Next Article in Journal
Chemical Derivatization in Flow Analysis
Next Article in Special Issue
α-Aminophosphonates, -Phosphinates, and -Phosphine Oxides as Extraction and Precipitation Agents for Rare Earth Metals, Thorium, and Uranium: A Review
Previous Article in Journal
Teucrium polium (L.): Phytochemical Screening and Biological Activities at Different Phenological Stages
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molecules
Volume 27
Issue 5
10.3390/molecules27051562
molecules-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

1-Aminoalkylphosphonium Derivatives: Smart Synthetic Equivalents of N-Acyliminium-Type Cations, and Maybe Something More: A Review †

by
Jakub Adamek
1,2,*,
Mirosława Grymel
1,2,3,
Anna Kuźnik
1,2 and
Agnieszka Październiok-Holewa
1,2
1
Department of Organic Chemistry, Bioorganic Chemistry and Biotechnology, Silesian University of Technology, B. Krzywoustego 4, 44-100 Gliwice, Poland
2
Biotechnology Center, Silesian University of Technology, B. Krzywoustego 8, 44-100 Gliwice, Poland
3
Department of Chemical Organic Technology and Petrochemistry, Faculty of Chemistry, Silesian University of Technology, B. Krzywoustego 4, 44-100 Gliwice, Poland
*
Author to whom correspondence should be addressed.
†
With a special dedication to Roman Mazurkiewicz in honor of the achievements within his career along with thanks from his scientific pupils.
Molecules 2022, 27(5), 1562; https://doi.org/10.3390/molecules27051562
Submission received: 26 January 2022 / Revised: 15 February 2022 / Accepted: 24 February 2022 / Published: 26 February 2022
(This article belongs to the Special Issue Organophosphorus Chemistry: A New Perspective)
Browse Figures
Versions Notes

Abstract

:
N-acyliminium-type cations are examples of highly reactive intermediates that are willingly used in organic synthesis in intra- or intermolecular α-amidoalkylation reactions. They are usually generated in situ from their corresponding precursors in the presence of acidic catalysts (Brønsted or Lewis acids). In this context, 1-aminoalkyltriarylphosphonium derivatives deserve particular attention. The positively charged phosphonium moiety located in the immediate vicinity of the N-acyl group significantly facilitates Cα-P+ bond breaking, even without the use of catalyst. Moreover, minor structural modifications of 1-aminoalkyltriarylphosphonium derivatives make it possible to modulate their reactivity in a simple way. Therefore, these types of compounds can be considered as smart synthetic equivalents of N-acyliminium-type cations. This review intends to familiarize a wide audience with the unique properties of 1-aminoalkyltriarylphosphonium derivatives and encourage their wider use in organic synthesis. Hence, the most important methods for the preparation of 1-aminoalkyltriarylphosphonium salts, as well as the area of their potential synthetic utilization, are demonstrated. In particular, the structure–reactivity correlations for the phosphonium salts are discussed. It was shown that 1-aminoalkyltriarylphosphonium salts are not only an interesting alternative to other α-amidoalkylating agents but also can be used in such important transformations as the Wittig reaction or heterocyclizations. Finally, the prospects and limitations of their further applications in synthesis and medicinal chemistry were considered.

Graphical Abstract

1. Introduction

α-Amidoalkylation reactions play an increasingly important role in organic synthesis as convenient and effective methods for the formation of C-C and C-heteroatom bonds, particularly of the intramolecular type, allowing the synthesis of carbo- or heterocyclic systems. In most cases, N-acylimine 2 or N-acyliminium cations 3 are the correct α-amidoalkylating agents and they are generated from precursors with the relevant structure 1 (Scheme 1) [1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23].
Many examples of α-amidoalkylating agent precursors and their applications in α-amidoalkylations have been reported in the literature. A brief summary is given in Table 1. Compared to the precursors described therein, 1-aminoalkylphosphonium derivatives are relatively unknown compounds. However, they have unique structural features which promote the generation of N-acyliminium-type cations. One of the most important is the presence of a positively charged phosphonium moiety (which easily departs as triarylphosphine PAr3) in the immediate vicinity of the acyl group.
Moreover, the reactivity of 1-aminoalkylphosphonium derivatives can be modulated by simple structural modifications, e.g., by changing the amino protecting group or by the introduction of electron-withdrawing substituents to the phosphonium moiety (replacing Ph3P by (3-C6H4Cl)3P or (4-C6H4CF3)3P; see Figure 1). Depending on the structure of the phosphonium salt used, the α-amidoalkylations may require a basic or acidic catalyst. However, the introduction of the abovementioned activating structural modifications allows one, in many cases, to conduct the reactions under milder and even catalyst-free conditions. Furthermore, such modifications not only affect the reactivity but also the course of the reaction (for example, to reduce side reactions), or even make it possible to change the type of reaction taking place (the α-amidoalkylation reaction vs the Wittig reaction).
The main purpose of this review paper is to organize and disseminate current knowledge about 1-aminoalkylphosphonium derivatives. To help understand the presented issues, three classes of these P-compounds have been distinguished. Three separate chapters are dedicated to them, where general properties, the most important methods for preparation as well as synthetic applications are described. Particularly, the correlation between the structure and the reactivity of phosphonium derivatives I-III is discussed. Scheme 2 provides a classification and a brief summary of the chemistry of 1-aminoalkylphosphonium derivatives.

2. 1-Aminoalkyltriarylphosphonium Derivatives

2.1. 1-(N-acylamino)alkylphosphonium Salts

Compounds with general formula 4 (Figure 2) are often called 1-(N-acylamino)alkylphosphonium salts, because a lot of the described models are amide derivatives (e.g., R1 = H, Me, Et, t-Bu, Ph, Bn, etc.; R3 = H). It is not an exact name because this group also includes lactams (e.g., R1, R3 = (CH2)3), carbamates (R1 = t-BuO, BnO; R3 = H) or urea derivatives (e.g., R1 = NMe2, R3 =H). In the α-position, there may be hydrogen (R2 = H), alkyl (R2 = Me, Et, i-Bu, etc.), aryl (R2 = Ph, 2-thienyl, 1-naphtyl, etc.) or more complex substituents (e.g., CH2CO2-t-Bu, CH2C6H4OBn, PO(OEt)2 etc.). The positively charged triarylphosphonium group PAr3 (Ar = Ph, 3-C6H4Cl, 4-C6H4CF3) is also directly bonded to Cα.
1-(N-acylamino)alkyltriphenylphosphonium salts 4 (Ar = Ph) are crystalline, stable at room temperature compounds that can be stored under laboratory conditions for a long time. They are well soluble in DCM and MeCN, but insoluble in diethyl ether. The most effective method of their purification is crystallization from DCM/Et2O or MeCN/Et2O systems. 1-(N-acylamino)alkyltriarylphosphonium salts 4 which are derivatives of triarylphosphines with electron-withdrawing substituents (Ar = 3-C6H4Cl or 4-C6H4CF3) are less stable. They are usually synthesized just before the reaction and used without purifiaction. The type of phosphonium group used has a huge impact on the reactivity of the whole molecule, which will be discussed later in this review.

2.1.1. Preparation

In the last century, most of the methods for the synthesis of 1-(N-acylamino)alkyltriarylphosphonium salts 4 concerned 1-(N-acylamino)methyltriphenylphosphonium salts (4a, R2 = H, Scheme 3). Between 1972 and 1991, Drach, Brovarets and co-workers [24,25,26,27] showed that 1-(N-acylamino)methylphosphonium chlorides (4a, X = Cl) can be obtained, in a simple reactions, by alkylation of triphenylphosphine (but also tributylphosphine PBu3 or hexaethylphosphorus triamide P(NEt2)3) with N-(chloromethyl)amides (5, Z = Cl) (Scheme 3, Method A). They also used N-(hydroxymethyl)amides (5, Z = OH) as alkylating agents, that were N-(chloromethyl)amides precursors (Scheme 3, Method A) [27]. In 1974, Devlin and Walker reported similar reactions, which were carried out at room temperature, using AcOEt as a solvent. They obtained 1-(N-benzoylamino)methyltriphenylphosphonium bromide or chloride (4a, X = Br or Cl) from N-(bromomethyl)benzamide or N-(chloromethyl)benzamide, respectively, in 54% and 69% yield (Scheme 3, Method A) [28]. Triphenylphosphine was also alkylated with N-(methoxymethyl)urea derivative 6 (Scheme 3, Method B). Reactions were carried out in methanol by bubbling HCl gas through the substrate solution or by treating it with aqueous HBr or HI [29]. 1-(N-alkoxycarbonyl)methyltriphenylphosphonium chlorides or bromides (4a, R1 = OR, X = Cl or Br) were obtained by Kozhushko et al. in the reaction of triphenylphosphine with chloromethylisocyanate or bromomethylisocyanate and further hydrolysis of the isocyanate group (Scheme 3, Method C) [30,31]. In analogous reactions, the corresponding triphenylphosphonium iodides (4a, R1 = OR, X = I) were also obtained by adding methyl iodide in the first step of the synthesis [32]. The same authors also described reactions in which phosphonium salts 4a (R1 = OR, X = Cl) were obtained by alkylation of triphenylphosphine with N-(chloromethyl)carbamates 10, that were previously generated from alcohol and methyl isocyanide (Scheme 3, Method D) [33]. In turn, Zinner and Fehlhammer described the two-stage method for the synthesis of 1-(N-formylamino)methyltriphenylphosphonium chloride 4a (R1 = H, X = Cl). Initially, they conducted the alkylation of triphenylphosphine using trimethylsilyl isocyanide in the presence of hexachloroethane in THF. The acidic hydrolysis of indirectly formed isocyanomethyltriphenylphosphonium chloride 11 finally yielded the expected phosphonium salt 4a (Scheme 3, Method E) [34]. However, the authors did not report the yield of the hydrolysis step.
Only a few of the described methods for synthesizing 1-(N-acylamino)methyltriphenylphosphonium salts 4a were based on other approaches than the alkylation of triphenylphosphine by N-(halomethyl)amides, their precursors or related compounds. One of these methods involved the alkylation of methyl carbamate with hydroxymethyltriphenylphosphonium chloride 12, which resulted in the production of 1-(N-methoxycarbonyl)aminomethyltriphenylphosphonium chloride 4a (R1 = OMe, X = Cl) in 73% yield (Scheme 3, Method F) [35]. Devlin and Walker demonstrated that the treatment of 2-bromo-2-nitrostyrene 14 with triphenylphosphine in methanol gave the phosphonium salt 15 in 47% yield. The vacuum pyrolysis of salt 15 at 150 °C, reduction with NaHBF4 in methanol or refluxing in chloroform with addition of bromine led to a mixture containing 1-(N-benzoylamino)methyltriphenylphosphonium bromide 4a (R1 = Ph, X = Br) as the main product (Scheme 3, Method G) [28,36].
There are few data available in the literature on the synthesis of 1-substituted phosphonium salts 4. In 1975, Drach et al. demonstrated that the reaction of triphenylphosphine with N-(1-benzoyl-1-chloromethyl)amides 16 led to triphenylphosphonium salts 17 with a benzoyl group at the 1-position. However, salts 17 turned out to be hygroscopic and unstable. Thus, the authors decided to transform them into more stable oxazolones 18 (Scheme 4) [37].
Next, Drach et al. described the route for the synthesis of various 1-(N-acylamino)-substituted vinylphosphonium salts 22, which was based on the condensation of triphenylphosphine with N-polychloroalkylamides 19 [38,39]. As reported by the authors, in the first step, the salts 20 were probably formed, which further split off hydrogen chloride, resulting in the formation of the corresponding vinylphosphonium salts 22, typically in yields above 90% (Scheme 5). 1-(N-acylamino)vinylphosphonium salts (AVPOSs) 22 are unique reagents for various types of heterocyclization, which was comprehensively discussed by Drach, Brovarets, and co-workers in 2002 [39].
At about the same time, Mazurkiewicz et al. started more extensive research on the synthesis of structurally diverse 1-(N-acylamino)alkyltriarylphosphonium salts 4. Wherein, the common feature of these methods was the raw materials, which was N-protected α-amino acids. The use of α-amino acids or their derivatives as substrates was greatly advantageous, due to almost unlimited availability and structural diversity of such compounds.
The first approach was based on using 4-triphenylphosphoranylidene-5(4H)-oxazolones 24 or 4-alkyl-4-triphenylphosphonio-5(4H)-oxazolones 25, obtained from glycine (Scheme 6) [40]. Phosphoranylidene-5(4H)-oxazolones 24, were hydrolyzed at room temperature in the presence of HBF4 to N-acyl-α-triphenylphosphonioglycines 26 (R2 = H, Scheme 6/A). Similarly, phosphonium iodides 25 were exposed to water in the mixture of THF/DCM, but without any acidic catalyst. Under these conditions, compounds 25 were transformed, in a few days, into N-acyl-1-triphenylphosphonio-α-amino acids 26 (R2 = Me, Scheme 6/B). In the next stage, 1-triphenylphosphonio-α-amino acids 26 were heated at 105–115 °C under reduced pressure (5 mmHg) or treated with diisopropylethylamine in DCM at 20 °C, which resulted in their decarboxylation to corresponding 1-(N-acylamino)alkyltriphenylphosphonium salts 4, usually in good yields (Scheme 6/C). The authors also showed, that in the case of hydrolysis of 4-alkyl-4-triphenylphosphonio-5(4H)-oxazolones 25 with a bulky substituent in the 4-position, the reaction proceeded with simultaneous decarboxylation and gave the expected 1-(N-acylamino)alkyltriphenylphosphonium salts 4 in one reaction step (Scheme 6/D) [41,42].
However, the two most important and general methods for the synthesis of 1-(N-acylamino)alkylphosphonium salts 4 were developed by Mazurkiewicz and Adamek in the last 10 years (Scheme 7) [43,44].
The first, three-stage method begins with the appropriate protection of α-amino acid functional groups (the NH2 group and other groups susceptible to electrochemical oxidation). Next, electrochemical decarboxylative α-methoxylation (or more generally, alkoxylation) takes place. As the authors noted, the electrochemical oxidations could be carried out in methanol with the addition of sodium methoxide as a base or in the presence of a solid-supported base (SiO2-Pip); wherein the latter process (based on a solid-supported base) proceeded in excellent yields and had a less complicated work-up. Recently, a simpler and even more efficient, standardized method for preparation of N,O-acetals 30 using the commercially available ElectraSyn 2.0 setup (graphite electrodes, Et3N as a base, room temp.) was described [45].
The last step is the substitution of the methoxy group in the reaction of N,O-acetals 30 with various types of phosphonium salts (Ar3P·HX, Scheme 7; Method A). The proposed method allows high yields (up to 99%) to be obtained not only for the simplest 1-(N-acylamino)alkylphosphonium salts 4 (e.g., R2 = H), but also for much more complex structure, including derivatives of phosphine with various substituents (Ar = Ph, 3-C6H4Cl, 4-C6H4CF3) [43,46]. Moreover, the raw material base can be expanded, since N-methoxyalkyl derivatives can be obtained by electrochemical oxidation of amides, carbamates or lactams. However, this is a less efficient process and an aqueous work-up of the reaction mixture is necessary [47].
In 2021, a procedure for the prepartion of N-protected aminoalkylphosphonium salts (including 1-(N-acylamino)alkylphosphonium ones) in one reaction step from aldehydes and either amides, carbamates, lactams, or urea in the presence of phosphonium salts 33 -Ar3P·HX (Scheme 7; Method B) was described [44]. Using a one-pot methodology, the simple work-up of the reaction mixture (no chromatography) makes 1-(N-acylamino)alkylphosphonium salts obtainable in high yields under relatively mild conditions (even at room temperature, but usually at 50 °C for 1 h). So far, it is the only general method of obtaining N-protected aminoalkylphosphonium salts without the use of electrochemical techniques [44]. Mechanistic studies showed that in the first step of the transformation, aldehydes and phosphonium salts (Ar3P·HX) form 1-hydroxyalkylphosphonium salts 34, which then react with amide-type substrates 31 to give the desired 1-(N-acylamino)alkylphosphonium salts 4 in good to excellent yields [44].
Next, it was shown that by conducting the reaction step-by-step and changing the order of the reacting compounds, 1-(N-acylamino)alkylphosphonium salts 4 could also be obtained. However, the procedure is effective only for formaldehyde (or paraformaldehyde). Hydroxymethylamides 35, already mentioned in the introduction (see also Table 1), are generated during such a transformation (Scheme 8). This method works well for the synthesis of N-protected aminomethyltriarylphosphonium salts 4a, but requires a catalyst (NaBr) and elevated temperatures (70–135 °C) [48].
The presented methods (Scheme 7 and Scheme 8) are based on a wide and diverse base of raw materials (α-amino acids, amide-type compounds, aldehydes), and provide easy access to structurally diverse 1-(N-acylamino)alkylphosphonium salts 4 also in the synthesis on a larger gram-scale [44,48].

2.1.2. Synthetic Utilization

Synthetic applications of 1-(N-acylamino)alkylphosphonium salts 4 are summarized in Figure 3. The high reactivity of such compounds is mainly related to the possibility of easy cleaving of the Cα-P+ bond (Scheme 9).
The strength of the Cα-P+ bond can be further reduced by introducing electron-withdrawing substituents to the phosphonium moiety (Scheme 10, Ar = 3-C6H4Cl and 4-C6H4CF3). The equilibrium in such systems was examined and described in 2018 [46]. As can be seen, it is shifted toward more stable and less reactive 1-(N-acylamino)alkylphosphonium salts (reactivity: PS-CF3 > PS-Cl > PS-H; stability: PS-CF3 < PS-Cl < PS-H).
The ease of formation of iminium-type cations 3 from phosphonium salts 4 was essential in the α-amidoalkylation reactions of various types of nucleophiles (C-nucleophiles and heteronucleophiles). In many cases, the generation of such reactive intermediates can proceed without the use of any catalysts, which is an amazing advantage compared to other α-amidoalkylating agents described in the literature (e.g., N-(1-methoxyalkyl)amides, α-amido sulfones, or N-(benzotriazolylalkyl)amides) [12,20].
One of the most widely described α-amidoalkylation reactions involving 1-(N-acylamino)alkylphosphonium salts is the reaction with P-nucleophiles: phosphites, phosphonites, or phosphinites. The products of these transformations are called phosphorus analogs of α-amino acids 37 (more precisely: 1-aminoalkanephosphonic acid derivatives, 1-aminoalkanephosphinic acid derivatives, or 1-aminoalkylphosphine oxide derivatives), and they are extremely interesting in terms of their biological activity [49].
Initially, the Michaelis–Arbuzov-type reaction with a double catalytic system was used for the synthesis of such compounds. A base (e.g., the Hünig’s base-(i-Pr)2EtN) facilitates the cleavage of the Cα-P+ bond and the formation of corresponding N-acylimine. In turn, the iodide anion (introduced as methyltriphenylphosphonium iodide) enables dealkylation of the intermediate alkoxyphosphonium salt 36 (Scheme 11) [50,51,52]. Further studies showed that the reaction could be carried out also under a catalytic-free conditions [46,52]. It was also possible, for the first time, to isolate and characterize one of the intermediates 36 (R1 = t-Bu; R2 = Me; R3, R4 = OR = OEt, Scheme 11), thus proving the reaction mechanism [46].
Unfortunately, the major disadvantage of these reactions is the complete racemization of the products. However, two solutions were proposed to overcome this drawback. The first was enzymatic kinetic resolution of products using Penicillin G acylase from Escherichia coli (Scheme 12, Method A) [53,54]. The second was changing the synthetic approach and to conduct organocatalytic α-amidoalkylation of P-nucleophiles (e.g., dimethyl phosphite; Michaelis–Becker-type reaction) by 1-(N-acylamino)alkyltriphenylphosphonium salts in PTC systems using Cinchona alkaloid derivatives 38 and 39 as catalysts (Scheme 12, Method B) [55].
Further research on phosphorus analogs of α-amino acids 37 revealed the possibility of transforming them into bisphosphoric acid esters 43, which also exhibit important biological activity (Scheme 13) [56,57].
Electrochemical alkoxylation of compounds 37 followed by substitution of the alkoxy group leads to 1-(N-acylamino)-1-triphenylphosphoniumalkylphosphonates 42. They can be also synthesized in a multi-stage procedure from imidate hydrochlorides 40 (Scheme 13).
As shown, the high reactivity of the phosphonium salts 42 can be used not only in the α-amidoalkylation reactions of phosphorus or carbon nucleophiles (Scheme 13, route A and B) but also in the elimination (Scheme 13; route C) or Wittig reaction (Scheme 13, route D) [57].
In the years between 2012 and 2021, Mazurkiewicz (triphenylphosphonium derivatives) and then Adamek (phosphonium salts with weakened Cα-P+ bond) explored the possibility of α-amidoalkylation of various other heteronucleophiles (Scheme 14) [46,51,58]. They demonstrated that, under appropriate conditions, N-protected 1-aminoalkyltriarylphosphonium salts 4 react with a wide variety of nucleophiles including mercaptans (PhCH2SH), phenol (PhOH), amines (PhCH2NH2), phthalimide, benzotriazole (BtH) or its salts (BtNa), and sodium aryl sulfinates (Ar2SO2Na) [46,51].
Initially, reactions were carried out at an elevated temperature (60 °C) in the presence of Hünig’s base (for 1-(N-acylamino)alkyltriphenylphosphonium salts 4, Ar = Ph, Scheme 14) [51]. The use of 1-(N-acylamino)alkyltriarylphosphonium salts 4 with a weakened Cα-P+ bond strength (Ar = 3-C6H4Cl, 4-C6H4CF3, Scheme 14) made it possible to conduct these reactions at room temperature without the use of catalysts [46].
The extraordinary α-amidoalkylating properties of 1-(N-acylamino)alkylphosphonium salts 4 also allow the α-amidoalkylation of “non-nucleophilic” bases, such as DBU (1,8-diazabicyclo(5.4.0)undec-7-ene), DBN (1,5-diazabicyclo(4.3.0)non-5-ene) or TBD (1,5,7-triazabicyclo(4.4.0)dec-5-ene; Scheme 14). The corresponding 1-(N-acylamino)alkylamidinium or guanidinium salts 52 are products in these reactions. They can be isolated but show limited stability; for example, salts 52 with a hydrogen at the β-position underwent transformation to enamides 53. As shown, enamides 53 can also be obtained directly from phosphonium salts 4 with an appropriate structure (hydrogen at the β-position) by an elimination reaction (Scheme 14) [58].
Interestingly, the 1-(N-acylamino)alkylphosphonium salts 4 can be converted to other α-amidoalkylating agents such as N-[1-(benzotriazol-1-yl)alkyl]amides 50 or α-amido sulfones 51. So far, they have been synthesized mainly in a three-component condensation of aldehyde with an amide-type substrate (amides, lactams, urea derivatives, etc.) in the presence of benzotriazole (BtH) or aryl sulfinates, respectively [12,20].
The proposed methodology extended the base of raw materials with N,O-acetals 30 obtained from α-amino acids or amide-type substrates in electrochemical oxidation (alkoxylation). As shown, 1-(N-acylamino)alkylphosphonium salts 4 do not have to be isolated in this type of transformation (Scheme 15A, see also Section 2.1.1, Scheme 7) [47,59].
Such transformations gained attention and were used for the preparation of substrates for α-amido sulfone-based intermolecular Mannich addition in the stereodivergent synthesis of lankacyclinol (Lankacidin antibiotics; Scheme 15/B) [60,61,62].
High reactivity of 1-(N-acylamino)alkylphosphonium salts 4 is also revealed in reactions with C-nucleophiles leading to the formation of β-aminocarbonyl systems 58 and 60. In the case of 1,3-dicarbonyl compounds 57 (dimethyl or diethyl malonate, ethyl acetoacetate, and ethyl 2-methylacetoacetate), it was necessary to use bases (DBU or LDA-lithium diisopropylamide) as catalysts to produce enolate anions [46,51]. However, the use of 1-(N-acylamino)alkyltriarylphosphonium salts 4 with a weakened Cα-P+ bond made it possible to conduct the reaction under slightly milder conditions (Scheme 16/A). This was similar in the reaction with 1-morpholinocyclohexene 59; replacing the triphenylphosphonium residue (Ar = Ph) with a triarylphosphonium group (Ar = 3-C6H4Cl or 4-C6H4CF3) facilitates the transformation (Scheme 16B) [46,51].
In 2018, Adamek et al. examined the reactivity of 1-(N-acylamino)alkyltriarylphosphonium salts 4 towards various aromatic systems (Scheme 17/A). It was demonstrated that phosphonium salts 4 react with arenes or heteroarenes under non-catalytic conditions. Reactions of triphenylphosphonium salts 4 (Ar = Ph, Scheme 17) required an elevated temperature and led to the formation of 1-arylalkylphosphonium salts 63 (non-classical α-amidoalkylation products). In turn, the use of 1-(N-acylamino)alkyltriarylphosphonium salts 4 with a weakened Cα-P+ bond made it possible to carry out the transformations to the expected classical products-N-(1-arylalkyl)amides 62 at room temperature. Moreover, it was found that 1-arylalkylphosphonium salts 63 are formed from N-(1-arylalkyl)amides 62 in the consecutive-type reaction what is included in the plausible mechanism proposed by the authors (Scheme 17/B) [63].
The spontaneous generation of reactive N-acyliminium cations from 1-(N-acylamino)alkyltriarylphosphonium salts 4 (under catalyst-free conditions) was also used in reactions with silyl enolates 66 or 67, to provide N-protected β-amino esters 68, as well as N-protected β-amino ketones 69 in good to excellent yields (Scheme 18/A). As Październiok-Holewa et al. demonstrated, the process can be carried out in THF at 50 °C or 60 °C using conventional heating or microwave irradiation. The proposed mechanism of the transformation included, in the first stage, the formation of the reactive N-acyliminium cation 3, which further reacts with the silyl enolate to give silyloxy-substituted carbenium ion 70, which fast undergoes a desilylation reaction to give β-amino carbonyl compounds 68 or 69 (Scheme 18/B) [64].
1-(N-acylamino)alkyltriarylphosphonium salts 4 are bifunctional compounds and their reactivity is not related only to the phosphonium moiety. Already in the 1980s, the transformation of N-acylaminomethyltriphenylphosphonium salts 4a into imidoyl chlorides 71 was described [26]. They turned out to be valuable reagents in cyclization reactions, in which heterocyclic systems such as oxazole, imidazole, tetrazole, or quinazolinone derivatives 72–76 can be obtained (Scheme 19/A–D) [26,65,66]. The presence of a triphenylphosphonium group enables further modification of the synthesized heterocycles, which was demonstrated in the example of the quinazolinones 75 (a structural motif of N-acylaminoalkylphosphonium salt can also be indicated here). These compounds undergo a reduction under mild conditions (Scheme 19/E). They can also be used as ylide precursors in the Wittig reaction with 4-nitrobenzaldehyde (Scheme 19/F) [26,65,66].

2.2. 1-Imidoalkyltriarylphosphonium Salts

Structures of the 1-imidoalkylphosphonium salts 79 described in the literature are based on a phthalimide (A = 1,2-C6H4) or succinimide (A = (CH2)2) ring (Figure 4). Two electron-withdrawing carbonyl groups connected to the nitrogen atom reduce the electron density at Cα, thus increasing its electrophilicity. In the α-position there may be hydrogen (R2 = H), alkyl (R2 = Me, Et, i-Bu) or aryl (R2 = Ph) substituent. Cα is also directly bonded to the triarylphosphonium group PAr3 (Ar = Ph, 4-C6H4Cl, 3-C6H4Cl, 4-C6H4CF3), which is positively charged and can act as a nucleofugal group.
In most cases, the 1-imidoalkylphosphonium salts are stable solids that can be stored under laboratory conditions for a long time. Interestingly, some of them also show biological activities such as cytotoxic or antimicrobial properties [67,68,69].

2.2.1. Preparation

In general, there is not much information in the literature on the methods for synthesis of 1-imidoalkylphosphonium salts 79, and most of them concern the simplest ones-imidomethylphosphonium salts (R2 = H). To the best of our knowledge, the first attempt to prepare imidomethylphosphonium salts was reported in 1961 by Hellmann and Schumacher [70]. It consisted in the reaction of phthalimidomethyltrimethylammonium iodide with triphenylphosphine in methanol. Such a reaction was later used several times; however, the structure of the substrate and conditions were slightly modified (mainly the solvent, temperature, and reaction time, Table 2).
After several decades, general methods for the synthesis of imidoalkylphosphonium salts appeared. The first one consisted of three stages: (A) the protection of amino group (from amino acids) by smelting phtalic, succinic or 1,8-naphthalic anhydride with the corresponding amino acid at 140–170 °C; (B) electrochemical decarboxylative α-methoxylation of 1-imidoalkanecarboxylic acids 81; (C) the displacement of the methoxy group by the triarylphosphine by smelting of the N-(1-methoxyalkyl)imides 82 with triarylphosphonium tetrafluoroborates in the presence of NaBr as catalyst (Scheme 20) [73].
Next, 1-imidoalkylphosphonium salts 79 were prepared in the three-component coupling of aldehydes and imides in the presence of triarylphosphonium salts Ar3P·HX (Scheme 21). An interesting fact is the formation of an intermediate hydroxyalkylphosphonium salt 34 in situ from aldehyde and triarylphosphonium salt (Ar3P·HX) during the reaction (see also Section 2.1.1, Scheme 7) [44].
As it was demonstrated, 1-imidomethylphosphonium salts 79 can also be obtained in the step-by-step procedure. This time, at first, formaldehyde (reactions with other aldehydes are ineffective) and imides form hydroxymethylimides 84 which, after isolation and purification, are reacted with triarylphosphonium salts 33 (Ar3P·HX) in the last stage (Scheme 22). The use of NaBr as a catalyst had a positive effect on the reaction (both on reaction time and yield) when Ar3P·HBF4 was used (for Ar3P·HBr no catalyst is needed) [48].
The last two methods allow for the fast synthesis of 1-imidoalkylphosphonium salts 79 (especially 1-imidomethylphosphonium salts) from readily available substrates, even on a larger scale (5–20 g). Besides, the advantage of both strategies is that they rely on non-electrochemical procedures, thus they are an interesting complement to previously described method.

2.2.2. Synthetic Utilization

The most important synthetic applications of 1-imidoalkylphosphonium salts 79 are summarized in Figure 5. Due to certain structural features (dicarbonyl protecting group and thus no NH proton), 1-imidoalkylphosphonium salts 79 can be considered as potential precursors of ylides in the Wittig reaction. These properties of phthalimidomethyltriphenylphosphonium bromide 79 were used by Tan and co-workers in the first stage of multi-step synthesis of compounds 85 and 86, which are known to modulate the activity of the TAAR1 receptor (the trace amine-associated receptor 1, see Table 3) [72].
Recently, the possibilities of using 1-imidoalkylphosphonium salts in imidoalkylation reactions with carbon- or heteronucleophiles have been explored.
In 2017, the Friedel–Crafts-type reaction of 1-imidoalkylphosphonium salts with various aromatic compounds was described. N-(1-arylalkyl)imides 87 were the main products of these transformations (Scheme 23) [73].
The presence of the dicarbonyl protection increases the electrophilicity of the Cα. In addition, the use of phosphonium salts which were derivatives of triarylphosphines with electron-withdrawing substituents make it easier to cleave the Cα-P+ bond (first step of the reaction, Scheme 23). Such structural modifications facilitated reactions with aromatic systems, also with weakly activated anisole and toluene (see Scheme 23 and compare the relation between the required reaction temperature and the type of phosphonium moiety). It is worth noting that, contrary to the reaction of the 1-(N-acylamino)alkylphosphonium salts 4 with arenes described in this review (Section 2.1.2), no consecutive reaction leading to the so-called non-classical α-amidoalkylation products (1-arylalkylphosphonium salts 63, see also Scheme 17) was observed. The only exception was the reaction of phosphonium salts 79-CF3 with 1,3,5-trimethoxybenzene (Scheme 24).
1-Imidoalkylphosphonium salts have also been used in the synthesis of imidoalkanephosphonates, imidoalkanephosphinates, and imidoalkylphosphine oxides. Generally, these compounds exhibit interesting biological properties, including antibacterial and antifungal activities or can be used in the synthesis of many bioactive compounds such as phosphapeptides (acting as enzyme inhibitors), oligonucleotides, cytotoxic agents (for example Cryptophycin 52) or 2,4,5-imidazolidinetriones (herbicides and plant growth regulators) [74,75].
The strategy for preparation of P-compounds 90 from phosphonium salts 79 was based on the Michaelis–Arbuzov-type reaction with the appropriate phosphorus nucleophiles (Scheme 25) [76].
It was observed that the reactivity of phosphonium salts 79 strongly depends on their structure. Good yields were obtained only from 1-(N-phthalimido)alkylphosphonium salt derivatives of tris(3-chlorophenyl)phosphine and tris(4-trifluoromethylphenyl)phosphine. However, a relatively large excess of phosphorus nucleophile and the addition of methyltriphenylphosphonium iodide (MePPh3+I−) as a catalyst that can facilitate the reaction were required (the most preferred molar ratio of reagents is 1:10:0.25 of phosphonium salt:P-nucleophile:catalyst).

2.3. N-acyl-1-phosphonio-α-amino Acid Esters

The general structural formula of N-acyl-1-phosphonio-α-amino acid esters 91 is shown in Figure 6. In most cases, structures of this kind of phosphonium salts described in the literature are based on a glycinate skeleton (R2 = H), although derivatives of other proteinogenic and non-proteinogenic α-amino acids, containing in the α position alkyl (R2 = Me, CH2OMe, CH2CN, CH2CH=CH2) or alkyl-aryl substituent (R2 = CH2Ph, CH2Bt) are also known. Cα is most often directly bonded to the positively charged triphenylphosphonium group (R = Ph), and less often tributhylphosphonium group (R = Bu). In the structure of the phosphonium salts in question, the carboxyl group is protected as an ethyl or methyl ester (R3 = Me, Et), while the protected amino group is present as an amide (R1 = Me, t-Bu, Ph) or carbamate (R1 = MeO, t-BuO, PhCH2O) moiety. The most common counterion to the positively charged phosphonium group is the tetrafluoroborate, bromide or iodide anion (X = BF4, Br, I).

2.3.1. Preparation

For a wide group of compounds belonging to N-acyl-1-triphenylphosphonio-α-amino acid esters 91, N-acyl-1-triphenylphosphonioglycinates (R2 = H) are the best known ones. They were prepared for the first time in 1983 by Kober and Steglich from ethyl N-acyl-1-bromoglycinates 93 by their reaction with triphenylphosphine. The starting 1-bromoglycine derivatives 93 were previously obtained in situ in the reaction of photochemical bromination of N-acylglycine ethyl esters 92 with bromine or N-bromosuccinimide carried out in tetrachloromethane (Scheme 26) [77].
In 1996, Mazurkiewicz and Pierwocha developed a simple route for the transformation of N-acylated glycine 94 into the 4-phosphoranylidene-5(4H)-oxazolones 24 [40]. The corresponding 5(4H)-oxazolone, obtained here as an intermediate in the reaction of the starting compound with DCC (N,N′-dicyclohexylcarbodiimide), is phosphorylated in situ with dibromotriphenylphosphorane (R3PBr2) in the presence of triethylamine. The resulting phosphoranylidene-5(4H)-oxazolones 24 can be further effectively converted into N-acyl-1-triphenylphosphonioglycinates (R2 = H), as well as esters of other N-acyl-1-triphenylphosphonio-α-amino acids 91 (Scheme 27).
However, the most convenient procedure for the synthesis of N-acyl-1-triphenylphosphonioglycinate tetrafluoroborates (91, X = BF4) is to treat a solution of phosphoranylidene-5(4H)-oxazolones 24 in methanol with an ethereal solution of tetrafluoroboric acid [78]. An alternative method for the synthesis of N-acyl-1-triphenylphosphonioglycinates with an iodide counterion (91, X = I) is a two-stage procedure that consists in the reaction of phosphoranylideneoxazolone 24 with acetyl iodide performed in acetonitrile, followed by the subsequent reaction of the acylation product with methanol [78,79]. Similarly, the synthesis of N-acyl-1-triphenylphosphonio-α-amino acids 91 with an alkyl substituent at the α-position (R2 ≠ H) by alkylation of 4-phosphoranylidene-5(4H)-oxazolones 24 with alkyl halides [80], and the next opening of the oxazolone ring under the treatment with methanol or methanol in the presence of an acidic catalyst was also described (Scheme 27) [81].
In 2004, three methods for the tranformation of N-alkoxycarbonyl-1-hydroxyglycinates 96 into especially interesting N-alkoxycarbonyl-1-triphenylphosphonioglycinates 91 (R1 = MeO, t-BuO, BnO) were developed by Mazurkiewicz et al. The proposed synthetic routes included the following transformations: phosphorylation of N-alkoxycarbonyl-1-hydroxyglycinates 96 with Ph3P·Br2 in the presence of Et3N (Procedure A), the reaction of N-alkoxycarbonyl-1-hydroxyglycinates 96 with DCC and Ph3P·HBF4 in the presence of Ph3P as a catalyst (Procedure B), and a new kind of the Mitsunobu reaction using Ph3P·HBF4 as a nucleophile conjugated acid (Procedure C, Scheme 28) [82].

2.3.2. Synthetic Utilization

N-Acyl-1-triphenylphosphonio-α-amino acid esters 91 are, in most cases, crystalline compounds, stable at room temperature, moderately sensitive to moisture, and well soluble in DCM and MeCN, but insoluble in diethyl ether. They can be easily purified by crystallization consisting of dissolution in DCM or MeCN at room temperature and precipitation with diethyl ether [78,79,80,81,82]. It is worth emphasizing that they are easily accessible from N-acylglycine even at kilogram scale (Scheme 26 and Scheme 27). All of these features of N-acyl-1-triphenylphosphonio-α-amino acid esters, as well as their diverse reactivity make these compounds interesting reagents in organic syntheses (Figure 7).
The directions of N-acyl-1-triphenylphosphonio-α-amino acid esters reactivity, and thus, the possibility of their further applications, were recognized during comprehensive research on their behavior in the presence of organic bases [83]. Reactions of N-acyl-1- triphenylphosphonio-α-amino acid methyl esters 91 with DBU and triethylamine were investigated then as the crucial step of the base catalysed displacement of the triphenylphosphonium group by various nucleophiles. Initially, this was observed by Kober, and Steglich, and later confirmed by Mazurkiewicz and Grymel, that N-acyl-1-triphenylphosphonioglycinates 91, upon treatment with bases, were converted into a mixture of the corresponding N-acyliminoacetate 97 and N-acyl-1-triphenylphosphoranylideneglycinate 98. Both the iminoacetate 97 and the ylide 98 turned out to be highly reactive, instable compounds that remained in an equilibrium and reacted slowly with each other providing the fumaric acid derivative 99. In the case of N-acyl-1-triphenylphosphonio-α-amino acid esters 91 with the quaternary α-carbon, the α-substituted homologues of N-acyliminoacetate 97 can undergo further tautomerization into the corresponding enamine 100 (Scheme 29) [83].
The application of N-acyl-1-triphenylphosphonioglycinates 91 as the precursors of phosphonium ylides 98 in the Wittig reaction with aliphatic or aromatic aldehydes in the presence of Et3N allowed the development of a simple and efficient procedure for the synthesis of α,β-dehydro-α-amino acid derivatives 101 (Scheme 29) [84].
On the other hand, methods for the displacement of the triphenylphosphonium group with a variety oxygen, sulfur, nitrogen and carbon nucleophilic agents, consisting in the addition of a nucleophile to the activated C=N double bond of the N-acylimino intermediate 97, opened up new routes for the synthesis of biologically important natural and unnatural non-proteinogenic α-amino acids by double functionalization of the glycine α-position with electrophilic and nucleophilic reagent (Scheme 30) [78,79,81].
N-acyl-1-triphenylphosphonio-α-amino acid esters 91 react easily with a wide variety of oxygen, sulphur and nitrogen nucleophiles including phenol (PhOH), mercaptans (t-BuSH, PhSH, PhCH2SH), imidazole, 4-nitroimidazole, pyrazole, benzotriazole, phthalimide, cyclohexylamine (Scheme 30) [78,81] and two kinds of carbon nucleophiles: enolates 103 of activated carbonyl compounds or enamines 105 (Scheme 31) [79]. Reactions were conducted in acetonitrile or methanol at room temperature in the presence of DBU or triethylamine, and the corresponding α-amino acid derivatives 102, 104, and 106 (including α,α-difunctionalized derivatives) were usually obtained in good to excellent yields [78,79,81].
This great interest in natural non-proteinogenic α-amino acids results from their diverse biological activities as antibiotics, pharmaceuticals, natural pesticides, and growth regulators, as well as their use in the synthesis of enzymes, hormones, new chemotherapeutics, synthetic immunostimulants, and other protein structured compounds [85,86]. The importance of α,α-disubstituted α-amino acids has been comprehensively discussed by many authors [87,88].
As demonstrated by Mazurkiewicz and Kuźnik, N-acyl-1-triphenylphosphonioglycinate tetrafluoroborates 91 are also convenient starting compounds for the transformation into N-acyl-α-(dialkoxyphosphoryl)glycinates 108 by the Michaelis–Arbuzow-type reaction with trimethylphosphite in the presence of methyltriphenylphosphonium iodide as a catalyst (Scheme 32) [89]. Among others, α-(dialkoxyphosphoryl)glycinates became the crucial synthetic tool commonly used for the synthesis of many natural products (including β-lactam antibiotics) or α,β-dehydro-α-amino acids by the Wadsworth-Emmons reaction [90,91,92,93,94,95,96]. As is known, hydrogenation of the latter compounds using chiral catalysts is considered to be one of the most general methods for the enantioselective synthesis of α-amino acids, including non-proteinogenic α-amino acids of diverse biological activities [97,98,99,100].
Although N-acyl-1-triphenylphosphonioglycinates 91 are relatively stable, they undergo interesting transformations at high temperatures. Thermogravimetric investigations revealed that during the process of the melting of salts 91, they underwent demethoxycarbonylation, providing N-acylaminomethyltriphenylphosphonium salts 4a (18–50%), along with methyltriphenylphosphonium salts (22–68%). When this reaction was performed in the presence of Ph3P and Ph3P∙HX (X = Br, BF4, I) the process of demethoxycarbonylation for N-acyl-1-triphenylphosphonioglycinate bromides and iodides (X = Br, I) occured at 95–130 °C in good to excellent yields (79–100%); whereas for N-acyl-1-triphenylphosphonioglycinate tetrafluoroborates 91 (X = BF4) as starting compounds, the analogous transformation occured at about 170–175 °C, giving the corresponding phosphonium tetrafluoroborates 4a in much lower yields (34–67%; Scheme 33) [101]. The practical significance of this process is due to the fact that the obtained 1-(N-acylamino)alkyltriphenylphosphonium salts 4a can be used as valuable α-amidoalkylating agents (see also Section 2.1.2).
The crucial structural motif for N-acyl-1-triphenylphosphonio-α-amino acid esters (amino, phosphonium and carbonyl groups bonded to the same carbon atom) can be a part of more complex systems. In this regard, 3-triphenylphosphonio-2,5-piperazinedione 111, 114 can be considered as structurally similar compounds to the phosphonium salts 91. They can be obtained from dipeptides in multistep procedure described by Mazurkiewicz and Gorewoda in 2011 [102]. The retention of configuration (position 6) results in the formation of chiral glycine cation equivalents 111, 114 which can be used for a diastereoselective nucleophilic substitution of the triphenylphosphonium group with S-, N-, P-, and C-nucleophiles (Scheme 34). Reactions were conducted at 0 or 25 °C in the presence of a base (i-Pr2EtN or DBU) and were particularly effective (high yields and high de%) for the proline derivative 111 [102].

3. Conclusions

1-Aminoalkylphosphonium derivatives are, in most cases, crystalline compounds, stable at room temperature and well soluble in chloroform, dichloromethane or acetonitrile, which makes them easy to store (even for a long time) and convenient to use reagents. On the other hand, they show remarkable reactivity especially towards various kinds of nucleophiles (both carbon- and heteronucleophiles). Moreover, the structure of such phosphonium salts is easy to modify by changing the N-protecting group or introducing electron-withdrawing or electron-donating substituents to the phosphonium moiety by using appropriately modified phosphines in the key stage of the synthesis. It allows for the control and, more interestingly, the targeting of the reactivity of these phosphonium compounds (α-amidoalkylation reaction vs. Wittig reaction).
All these factors make the 1-aminoalkylphosphonium derivatives an interesting group of “smart-reagents” with great potential as precursors of reactive intermediates such as N-acyliminium-type cations (generated without the need for any catalysts), or ylides. This was used in the synthesis of such compounds as phosphorus analogs of α-amino acids, β-aminocarbonyl systems, 1-arylalkylphosphonium salts or α,β-dehydro-α-amino acids, which are very important because of their valuable biological and chemical properties. However, most of the described reactions were intermolecular (did not lead to cyclization) and were not conducted in a stereocontrolled manner. These two aspects require further research because such transformations are of great importance in the synthesis of natural, biologically active compounds. It seems that, especially in this field, the easy ability to control the Cα-P+ bond strength and introduce structural modifications within phosphonium salts may be crucial (Figure 8—new challenges/asymmetric synthesis/cyclization). Studies on cyclization and stereocontrol of reactions involving 1-aminoalkylphosphonium salts are in progress.
It is worth adding that, not only many of the described compounds obtained from 1-aminoalkylphosphonium salts derivatives, but also some phosphonium salts themselves show interesting biological properties. However, in this case, the area of potential application should also be much more explored. 1-Aminoalkylphosphonium salts derivatives can be an ideal tool for the modification of already known structures with proven biological activity. Furthermore, recent reports on mitochondria-targeted phosphonium salts inspire the design and synthesis of molecular hybrids or conjugates that will use the targeting properties of the triphenylphosphonium (TPP) group, its biological properties, or both (Figure 8—new challenges/biological activity).
We hope that the presented data will encourage further research on 1-aminoalkylphosphonium salt derivatives and will contribute to discovering their full potential.

Author Contributions

Conceptualization, J.A.; data curation, J.A., M.G., A.K. and A.P.-H.; writing—original draft preparation, J.A., M.G., A.K. and A.P.-H.; writing—review and editing, J.A., M.G., A.K. and A.P.-H.; supervision, J.A. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported under the Rector’s Habilitation Grant, Silesian University of Technology (Poland), No. 04/020/RGH20/1006. This research was also supported by Silesian University of Technology (Poland) Grant BK No. 04/050/BK_21/0116.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Neto, B.A.D.; Rocha, R.O.; Rodrigues, M.O. Catalytic Approaches to Multicomponent Reactions: A Critical Review and Perspectives on the Roles of Catalysis. Molecules 2022, 27, 132. [Google Scholar] [CrossRef]
  2. Kokkala, P.; Rajeshkumar, T.; Mpakali, A.; Stratikos, E.; Vogiatzis, K.D.; Georgiadis, D. A Carbodiimide-Mediated P–C Bond-Forming Reaction: Mild Amidoalkylation of P-Nucleophiles by Boc-Aminals. Org. Lett. 2021, 23, 1726–1730. [Google Scholar] [CrossRef]
  3. Heravi, M.M.; Zadsirjan, V.; Heydari, M.; Masoumi, B. Organocatalyzed Asymmetric Friedel-Crafts Reactions: An Update. Chem. Rec. 2019, 19, 2236–2340. [Google Scholar] [CrossRef]
  4. Aranzamendi, E.; Sotomayor, N.; Lete, E. Phenolic Activation in Chiral Brønsted Acid-Catalyzed Intramolecular α-Amidoalkylation Reactions for the Synthesis of Fused Isoquinolines. ACS Omega 2017, 2, 2706–2718. [Google Scholar] [CrossRef] [Green Version]
  5. Huang, Y.-Y.; Cai, C.; Yang, X.; Lv, Z.-C.; Schneider, U. Catalytic Asymmetric Reactions with N,O-Aminals. ACS Catal. 2016, 6, 5747–5763. [Google Scholar] [CrossRef]
  6. Kataja, A.O.; Masson, G. Imine and iminium precursors as versatile intermediates in enantioselective organocatalysis. Tetrahedron 2014, 70, 8783–8815. [Google Scholar] [CrossRef]
  7. Maryanoff, B.E.; Zhang, H.C.; Cohen, J.H.; Turchi, I.J.; Maryanoff, C.A. Cyclizations of N-acyliminium ions. Chem. Rev. 2004, 104, 1431–1628. [Google Scholar] [CrossRef]
  8. Yazici, A.; Pyne, S.G. Intermolecular addition reactions of N-acyliminium ions (Part I). Synthesis 2009, 339–368. [Google Scholar] [CrossRef] [Green Version]
  9. Yazici, A.; Pyne, S.G. Intermolecular addition reactions of N-acyliminium ions (Part II). Synthesis 2009, 513–541. [Google Scholar] [CrossRef] [Green Version]
  10. Aranzamendi, E.; Arrasate, S.; Sotomayor, N.; González-Díaz, H.; Lete, E. Chiral Brønsted Acid Catalyzed Enantioselective α-Amidoalkylation Reactions: A Joint Experimental and Predictive Study. ChemistryOpen 2016, 5, 540–549. [Google Scholar] [CrossRef] [Green Version]
  11. Zhang, S.; Shi, X.; Li, J.; Hou, Z.; Song, Z.; Su, X.; Peng, D.; Wang, F.; Yu, Y.; Zhao, G. Nickel-Catalyzed Amidoalkylation Reaction of γ-Hydroxy Lactams: An Access to 3-Substituted Isoindolinones. ACS Omega 2019, 4, 19420–19436. [Google Scholar] [CrossRef] [Green Version]
  12. Mazurkiewicz, R.; Październiok-Holewa, A.; Adamek, J.; Zielińska, K. α-Amidoalkylating agents: Structure, synthesis, reactivity and application. Adv. Heterocycl. Chem. 2014, 111, 43–94. [Google Scholar] [CrossRef]
  13. Touati, B.; El Bouakher, A.; Taillier, C.; Othman, R.B.; Trabelsi-Ayadi, M.; Antoniotti, S.; DuÇach, E.; Dalla, V. Enolizable Carbonyls and N,O-Acetals: A Rational Approach for Room-Temperature Lewis Superacid-Catalyzed Directa-Amidoalkylation of Ketones and Aldehydes. Chem. Eur. J. 2016, 22, 6012–6022. [Google Scholar] [CrossRef] [PubMed]
  14. Schneider, A.E.; Manolikakes, G. Bi(OTf)3-Catalyzed Multicomponent α-Amidoalkylation Reactions. J. Org. Chem. 2015, 80, 6193–6212. [Google Scholar] [CrossRef] [PubMed]
  15. Vinogradov, M.G.; Olga, V.; Turova, O.V.; Zlotin, S.G. The progress in the chemistry of N-acyliminium ions and their use in stereoselective organic synthesis. Russ. Chem. Rev. 2017, 86, 1–17. [Google Scholar] [CrossRef]
  16. Katritzky, A.R.; Abdel-Fattah, A.A.A.; Celik, I. Benzotriazole-mediated amidoalkylations of nitroalkanes, nitriles, alkynes and esters. ARKIVOC 2007, 11, 96–113. [Google Scholar] [CrossRef] [Green Version]
  17. Katritzky, A.R.; Manju, K.; Singh, S.K.; Meher, N.K. Benzotriazole mediated amino-, amido-, alkoxy- and alkylthioalkylation. Tetrahedron 2005, 61, 2555–2581. [Google Scholar] [CrossRef]
  18. Katritzky, A.R.; Mehta, S.; He, H.Y. Syntheses of Pyrrolo- and Indoloisoquinolinones by Intramolecular Cyclizations of 1-(2-Arylethyl)-5-benzotriazolylpyrrolidin-2-ones and 3-Benzotriazolyl-2-(2-arylethyl)-1-isoindolinones. J. Org. Chem. 2001, 66, 148–152. [Google Scholar] [CrossRef] [PubMed]
  19. Katritzky, A.R.; Kirichenko, K.; Elsayed, A.M.; Ji, Y.; Fang, Y. Convenient Preparation of tert-Butyl β-(Protected amino)esters. J. Org. Chem. 2002, 67, 4957–4959. [Google Scholar] [CrossRef]
  20. Petrini, M. α-Amido Sulfones as Stable Precursors of Reactive N-Acylimino Derivatives. Chem. Rev. 2005, 105, 3949–3977. [Google Scholar] [CrossRef]
  21. Ballini, R.; Palmieri, A.; Petrini, M.; Torregiani, E. Solventless Clay-Promoted Friedel−Crafts Reaction of Indoles with α-Amido Sulfones:  Unexpected Synthesis of 3-(1-Arylsulfonylalkyl) Indoles. Org. Lett. 2006, 8, 4093–4096. [Google Scholar] [CrossRef]
  22. Das, B.; Damodar, K.; Bhunia, N. A Simple and Efficient Access to α-Amino Phosphonates from N-Benzyloxycarbonylamino Sulfones Using Indium(III) Chloride. J. Org. Chem. 2009, 74, 5607–5609. [Google Scholar] [CrossRef] [PubMed]
  23. Marcantoni, E.; Palmieri, A.; Petrini, M. Recent synthetic applications of α-amido sulfones as precursors of N-acylimino derivatives. Org. Chem. Front. 2019, 6, 2142–2182. [Google Scholar] [CrossRef]
  24. Drach, B.; Kirsanov, A.; Sviridov, E. Reaction of N-chloromethyl amides of acids with triphenylphosphine. Zh. Obshch. Khim. 1972, 42, 953–954. [Google Scholar]
  25. Smolii, O.B.; Brovarets, V.S.; Drach, B.S. Substituted Methylphosphonium Salts with an Imidoyl Chloride Group. Zh. Obshch. Khim. 1986, 56, 2802–2803. [Google Scholar]
  26. Smolii, O.B.; Brovarets, V.S.; Pirozhenko, V.V.; Drach, B.S. Cyclocondensation of N-Substituted Imidoyl Chlorides Containing a Phosphonium Group. Zh. Obshch. Khim. 1988, 58, 2465–2471. [Google Scholar]
  27. Kasukhin, L.F.; Brovarets, V.S.; Smolii, O.B.; Kurg, V.V.; Budnik, L.V.; Drach, B.S. N-Acylaminomethyl and Substituted 1-Acylaminoethenylphosphonium Salts As Inhibitors of Acetylcholinesterase. Zh. Obshch. Khim. 1991, 61, 2679–2684. [Google Scholar]
  28. Devlin, C.J.; Walker, B.J. Reactions of bromonitroalkenes with tervalent phosphorus. Part II. Reaction in methanol. J. Chem. Soc. Perkin Trans. 1974, 1, 453–460. [Google Scholar] [CrossRef]
  29. Petersen, H.; Reuther, W. α-Ureidoalkylierung von Phosphor (III)-Verbindungen. Justus Liebigs Ann. Chem. 1972, 766, 58–72. [Google Scholar] [CrossRef]
  30. Kozhushko, B.N.; Gumenyuk, A.V.; Palichuk, Y.A.; Shokol, V.A. Trialkyl- et Triaryl-(Isocyanatomethyl) Chlorophosphoranes. Zh. Obshch. Khim. 1977, 47, 333–339. [Google Scholar]
  31. Shokol, V.A.; Silina, E.B.; Kozushko, B.N.; Golik, G.A. Bromomethyl Isocyanate and Its Phosphorylated Derivatives. Zh. Obshch. Khim. 1979, 49, 312–316. [Google Scholar]
  32. Kozhushko, B.N.; Silina, E.B.; Gumenyuk, A.V.; Turov, A.V.; Shokol, V.A. Triaryl(Isocyanatomethyl)Phosphonium Iodides. Zh. Obshch. Khim. 1980, 50, 2210–2215. [Google Scholar]
  33. Shokol, V.A.; Kozushko, B.N.; Gumenyuk, A.V. Trialkyl- And Aryldialkyl(Isocyanatomethyl)Ammonium Chlorides. Zh. Obshch. Khim. 1977, 47, 1110–1118. [Google Scholar]
  34. Zinner, G.; Fehlhammer, W.P. Isocyanomethylenetriphenylphosphorane. Angew. Chem. Int. Ed. Engl. 1985, 24, 979–980. [Google Scholar] [CrossRef]
  35. Frank, A.W.; Drake, G.L. Synthesis and properties of carbamate derivatives of tetrakis(hydroxymethyl)phosphonium chloride. J. Org. Chem. 1977, 42, 4040–4045. [Google Scholar] [CrossRef]
  36. Devlin, C.J.; Walker, B.J. A possible azirine intermediate in the reaction of bromonitroalkenes with triphenylphosphine. J. Chem. Soc. D Chem. Comm. 1970, 917–918. [Google Scholar] [CrossRef]
  37. Drach, B.S.; Dolgushina, I.Y.; Sinitsa, A.D. Application of Omega-Chloro-Omega-Acylamidoacetophenones for Synthesis of Phosphorylated Oxazoles. Zh. Obshch. Khim. 1975, 45, 1251–1255. [Google Scholar]
  38. Brovarets, V.S.; Lobanov, O.P.; Vinogradova, T.K.; Drach, B.S. Preparation and Properties of 2-Chloro-1-Acylaminovinyltriphenylphosphonium Chlorides. Zh. Obshch. Khim. 1984, 54, 288–301. [Google Scholar]
  39. Drach, B.S.; Brovarets, V.S.; Smolii, O.B. Acylamino-Substituted Vinylphosphonium Salts in Syntheses of Derivatives of Nitrogen Heterocycles. Russ. J. Gen. Chem. 2002, 72, 1661–1687. [Google Scholar] [CrossRef]
  40. Mazurkiewicz, R.; Pierwocha, A.W. Phosphoranylidene-5(4H)-oxazolones–A novel synthesis and properties. Monatsh. Chem. 1996, 127, 219–225. [Google Scholar] [CrossRef]
  41. Mazurkiewicz, R.; Październiok-Holewa, A.; Grymel, M. Synthesis and decarboxylation of N-acyl-α-triphenylphosphonio-α-amino acids: A new synthesis of α-(N-acylamino)alkyltriphenylphosphonium salts. Tetrahedron Lett. 2008, 49, 1801–1803. [Google Scholar] [CrossRef]
  42. Mazurkiewicz, R.; Październiok-Holewa, A.; Grymel, M. N-Acyl-α-triphenylphosphonio-α-amino Acids: Synthesis and Decarboxylation to α-(N-Acylamino)alkyltriphenylphosphonium Salts. Phosphorus Sulfur Silicon Relat. Elem. 2009, 184, 1017–1027. [Google Scholar] [CrossRef]
  43. Mazurkiewicz, R.; Adamek, J.; Październiok-Holewa, A.; Zielińska, K.; Simka, W.; Gajos, A.; Szymura, K. α-Amidoalkylating Agents from N-Acyl-α-amino Acids: 1-(N-Acylamino)alkyltriphenylphosphonium Salts. J. Org. Chem. 2012, 77, 1952–1960. [Google Scholar] [CrossRef] [PubMed]
  44. Adamek, J.; Zieleźny, P.; Erfurt, K. N-protected 1-aminoalkylphosphonium salts from amides, carbamates, lactams, or imides. J. Org. Chem. 2021, 86, 5852–5862. [Google Scholar] [CrossRef]
  45. Walęcka-Kurczyk, A.; Adamek, J.; Walczak, K.; Michalak, M.; Październiok-Holewa, A. Non-Kolbe electrolysis of N-protected-α-amino acids: A standardized method for the synthesis of N-protected (1-methoxyalkyl)amines. RSC Adv. 2022, 12, 2107–2114. [Google Scholar] [CrossRef]
  46. Adamek, J.; Węgrzyk, A.; Kończewicz, J.; Walczak, K.; Erfurt, K. 1-(N-Acylamino)alkyltriarylphosphonium Salts with Weakened Cα-P+ Bond Strength—Synthetic Applications. Molecules 2018, 23, 2453. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Adamek, J.; Mazurkiewicz, R.; Październiok-Holewa, A.; Grymel, M.; Kuźnik, A.; Zielińska, K. 1-(N-Acylamino)alkyl Sulfones from N-Acyl-α-amino Acids or N-Alkylamides. J. Org. Chem. 2014, 79, 2765–2770. [Google Scholar] [CrossRef]
  48. Kozicka, D.; Zieleźny, P.; Erfurt, K.; Adamek, J. Amide-type substrates in the synthesis of N-protected 1-aminomethylphosphonium salts. Catalysts 2021, 11, 552. [Google Scholar] [CrossRef]
  49. Mucha, A.; Kafarski, P.; Berlicki, L. Remarkable Potential of the α-Aminophosphonate/Phosphinate Structural Motif in Medicinal Chemistry. J. Med. Chem. 2011, 54, 5955–5980. [Google Scholar] [CrossRef] [PubMed]
  50. Mazurkiewicz, R.; Październiok-Holewa, A.; Kononienko, A. A Novel Synthesis of 1-Aminoalkanephosphonic Acid Derivatives from 1-(N-Acylamino)alkyltriphenylphosphonium Salts. Phosphorus Sulfur Silicon 2010, 185, 1986–1992. [Google Scholar] [CrossRef]
  51. Październiok-Holewa, A.; Adamek, J.; Mazurkiewicz, R.; Zielińska, K. Amidoalkylating Properties of 1-(N-Acylamino)Alkyltriphenylphosphonium Salts. Phosphorus Sulfur Silicon Relat. Elem. 2013, 188, 205–212. [Google Scholar] [CrossRef]
  52. Adamek, J.; Październiok-Holewa, A.; Zielińska, K.; Mazurkiewicz, R. Comparative Studies on the Amidoalkylating Properties of N-(1-Methoxyalkyl)Amides and 1-(N-Acylamino)Alkyltriphenylphosphonium Salts in the Michaelis–Arbuzov-Like Reaction: A New One-Pot Transformation of N-(1-Methoxyalkyl)Amides into Phosphonic or Phosphinic Analogs of N-Acyl-α-Amino Acids. Phosphorus Sulfur Silicon Relat. Elem. 2013, 188, 967–980. [Google Scholar] [CrossRef]
  53. Zielińska, K.; Mazurkiewicz, R.; Szymańska, K.; Jarzębski, A.; Magiera, S.; Erfurt, K. Penicillin G Acylase-Mediated Kinetic Resolution of Racemic 1-(N-Acylamino)alkylphosphonic and 1-(N-Acylamino)alkylphosphinic Acids and Their Esters. J. Mol. Catal. B Enzym. 2016, 132, 31–40. [Google Scholar] [CrossRef]
  54. Zielińska, K.; Mazurkiewicz, R.; Szymańska, K.; Jarzębski, A. Batch and in-flow kinetic resolution of racemic 1-(N-acylamino)alkylphosphonic and 1-(N-acylamino)alkylphosphinic acids and their esters using immobilized penicillin G acylase. Tetrahedron Asymmetry 2017, 28, 146–152. [Google Scholar] [CrossRef]
  55. Walęcka-Kurczyk, A.; Walczak, K.; Kuźnik, A.; Stecko, S.; Październiok-Holewa, A. The Synthesis of α-Aminophosphonates via Enantioselective Organocatalytic Reaction of 1-(N-Acylamino)alkylphosphonium Salts with Dimethyl Phosphite. Molecules 2020, 25, 405. [Google Scholar] [CrossRef] [Green Version]
  56. Kuźnik, A.; Mazurkiewicz, R.; Grymel, M.; Zielińska, K.; Adamek, J.; Chmielewska, E.; Bochno, M.; Kubica, S. New method for the synthesis of α-aminoalkylenebisphosphonates and their asymmetric phosphonyl-phosphinyl and phosphonyl-phosphinoyl analogues. Beilstein J. Org. Chem. 2015, 11, 1418–1424. [Google Scholar] [CrossRef] [Green Version]
  57. Kuźnik, A.; Mazurkiewicz, R.; Zięba, M.; Erfurt, K. 1-(N-Acylamino)-1-triphenylphosphoniumalkylphosphonates: General synthesis and prospects for further synthetic applications. Tetrahedron Lett. 2018, 59, 3307–3310. [Google Scholar] [CrossRef]
  58. Październiok-Holewa, A.; Adamek, J.; Zielińska, K.; Piernikarczyk, K.; Mazurkiewicz, R. N-(1-acyloaminoalkyl)amidinium salts derived from DBU or related bases as reactive intermediates in α-amidoalkylation reactions. Arkivoc 2012, 4, 314–329. [Google Scholar] [CrossRef] [Green Version]
  59. Adamek, J.; Mazurkiewicz, R.; Październiok-Holewa, A.; Kuźnik, A.; Grymel, M.; Zielińska, K.; Simka, W. N-[1-(Benzotriazol-1-yl)alkyl]amides from N-acyl-α-amino acids or N-alkylamides. Tetrahedron 2014, 70, 5725–5729. [Google Scholar] [CrossRef]
  60. Zheng, K.; Shen, D.; Zhang, B.; Hong, R. Stereodivergent Synthesis of Lankacyclinol and Its C2/C18-Congeners Enabled by a Bioinspired Mannich Reaction. J. Org. Chem. 2021, 86, 10991–11005. [Google Scholar] [CrossRef]
  61. Zheng, K.; Shen, D.; Zhang, B.; Hong, R. Landscape of Lankacidin Biomimetic Synthesis: Structural Revisions and Biogenetic Implications. J. Org. Chem. 2020, 85, 13818–13836. [Google Scholar] [CrossRef]
  62. Zheng, K.; Hong, R. The Fruit of Gold: Biomimicry in the Syntheses of Lankacidins. Acc. Chem. Res. 2021, 54, 3438–3451. [Google Scholar] [CrossRef]
  63. Adamek, J.; Węgrzyk, A.; Krawczyk, M.; Erfurt, K. Catalyst-free Friedel-Crafts reaction of 1-(N-acylamino)alkyltriarylphosphonium salts with electron-rich arenes. Tetrahedron 2018, 74, 2575–2583. [Google Scholar] [CrossRef]
  64. Październiok-Holewa, A.; Walęcka-Kurczyk, A.; Musioł, S.; Stecko, S. Catalyst-free Mannich-type reaction of 1-(N-acylamino)alkyltriphenylphosphonium salts with silyl enolates. Tetrahedron 2019, 75, 732–742. [Google Scholar] [CrossRef]
  65. Smolii, O.B.; Brovarets, V.S.; Drach, B.S. Reaction of the Chloride of N-(Triphenylphosphoniomethyl)benzimidoyl chloride with Sodium Rhodanide. Zh. Obshch. Khim. 1987, 57, 2145–2146. [Google Scholar]
  66. Smolii, O.B.; Brovarets, V.S.; Drach, B.S. Reaction of the Chloride of N-(Triphenylphosphoniomethyl)benzimidoyl chloride with Carboxylic Acid Chlorides. Zh. Obshch. Khim. 1988, 58, 1670–1671. [Google Scholar]
  67. Dubois, R.J.; Lin, C.-C.; Beisler, J.A. Synthesis and antitumor properties of some isoindolylalkylphosphonium salts. J. Med. Chem. 1978, 21, 303–306. [Google Scholar] [CrossRef]
  68. Tessier, D.; Filteau, M.; Radu, I. New Antimicrobial Compositions and Uses Thereof. U.S. Patent US 2015/0201622 Al, 23 July 2015. [Google Scholar]
  69. Tessier, D.; Filteau, M.; Radu, I. Antimicrobial Solution Comprising a Metallic Salt and a Surfactant. International Patent WO 2006105669 A1, 12 October 2006. [Google Scholar]
  70. Hellmann, H.; Schumacher, O. Quartäre Phosphoniumsalze aus tertiären Phosphinen und quartären Ammoniumsalzen. Justus Liebigs Ann. Chem. 1961, 640, 79–84. [Google Scholar] [CrossRef]
  71. Enzmann, A.; Eckert, M.; Ponikwar, W.; Polborn, K.; Schneiderbauer, S.; Beller, M.; Beck, W. Aminomethyl and Aminoacetyl Complexes of Palladium(II), Platinum(II), Iron(II) and Rhenium(I) with N-Phthaloyl as Amino Protecting Group and Mechanistic Studies on the Palladium-Catalyzed Amidocarbonylation. Eur. J. Inorg. Chem. 2004, 6, 1330–1340. [Google Scholar] [CrossRef]
  72. Tan, E.S.; Naylor, J.C.; Groban, E.S.; Bunzow, J.R.; Jacobson, M.P.; Grandy, D.K.; Scanlan, T.S. The Molecular Basis of Species-Specific Ligand Activation of Trace Amine-Associated Receptor 1 (TAAR1). ACS Chem. Biol. 2009, 4, 209–220. [Google Scholar] [CrossRef] [Green Version]
  73. Adamek, J.; Mazurkiewicz, R.; Węgrzyk, A.; Erfurt, K. 1-Imidoalkylphosphonium salts with modulated Cα-P+ bond strength: Synthesis and application as new active α-imidoalkylating agents. Beilstein J. Org. Chem. 2017, 13, 1446–1455. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  74. Clavé, G.; Reverte, M.; Vasseur, J.-J.; Smietana, M. Modified internucleoside linkages for nuclease-resistant oligonucleotides. RSC Chem. Biol. 2021, 2, 94–150. [Google Scholar] [CrossRef]
  75. Nahrwold, M.; Bogner, T.; Eissler, S.; Verma, S.; Sewald, N. “Clicktophycin-52”: A Bioactive Cryptophycin-52 Triazole Analogue. Org. Lett. 2010, 12, 1064–1067. [Google Scholar] [CrossRef] [PubMed]
  76. Adamek, J.; Węgrzyk-Schlieter, A.; Steć, K.; Walczak, K.; Erfurt, K. Michaelis-Arbuzov-Type Reaction of 1-Imidoalkyltriarylphosphonium Salts with Selected Phosphorus Nucleophiles. Molecules 2019, 24, 3405. [Google Scholar] [CrossRef] [Green Version]
  77. Kober, R.; Steglich, W. Untersuchungen zur Reaktion von Acylaminobrommalonestern und Acylaminobromessigestern mit Trialkylphosphiteneine einfache Synthese von 2-Amino-2-(diethoxyphosphoryl) Essigsäure Ethylester. Liebigs Ann. Chem. 1983, 4, 599–609. [Google Scholar] [CrossRef]
  78. Mazurkiewicz, R.; Grymel, M. N-Acyl-α-triphenylphosphonioglycinates: A Novel Cationic Glycine Equivalent and its Reactions with Heteroatom Nucleophiles. Monatsh. Chem. 1999, 130, 597–604. [Google Scholar] [CrossRef]
  79. Mazurkiewicz, R.; Grymel, M. A new synthesis of α-amino acid derivatives by reaction of N-acyl-α-triphenylphosphonioglycinates with carbon nucleophiles. Phosporus Sulfur Silicon 2000, 164, 33–43. [Google Scholar] [CrossRef]
  80. Mazurkiewicz, R.; Pierwocha, A.W. 4-Phosphoranylidene-5(4H)-oxazolones II. Reactions with alkylating agents. Monatsh. Chem. 1997, 128, 893–900. [Google Scholar] [CrossRef]
  81. Grymel, M.; Kuźnik, A.; Mazurkiewicz, R. N-Acyl-α-triphenylphosphonio-α-amino acid esters as synthetic equivalents of α-amino acid α-cations. Phosporus Sulfur Silicon 2015, 190, 429–439. [Google Scholar] [CrossRef]
  82. Mazurkiewicz, R.; Grymel, M.; Kuźnik, A. Three New in situ Syntheses of N-Acyl-α-triphenylphosphonioglycinates. Monatsh. Chem. 2004, 135, 799–806. [Google Scholar] [CrossRef]
  83. Mazurkiewicz, R.; Grymel, M. Reaction of N-Acyl-α-triphenylphosphonio-α-amino Acid Esters with Organic Bases: Mechanism of the Base-Catalyzed Nucleophilic Substitution of the Triphenylphosphonium Group. Monatsh. Chem. 2002, 133, 1197–1204. [Google Scholar] [CrossRef]
  84. Mazurkiewicz, R.; Kuźnik, A.; Grymel, M.; Kuźnik, N. N-Acyl-α-triphenylphosphonioglycinates in the Synthesis of α,β-Dehydro-α-amino Acid Derivatives. Monatsh. Chem. 2004, 135, 807–815. [Google Scholar] [CrossRef]
  85. Gentilucci, L.; De Marco, R.; Cerisoli, L. Chemical Modifications Designed to Improve Peptide Stability: Incorporation of Non-Natural Amino Acids, Pseudo-Peptide Bonds, and Cyclization. Curr. Pharm. Des. 2010, 16, 3185–3203. [Google Scholar] [CrossRef]
  86. Meester, W.J.N.; van Maarseveen, J.H.; Schoemaker, H.E.; Hiemstra, H.; Rutjes, F.P.J.T. Glyoxylates as Versatile Building Blocks for the Synthesis of α-Amino Acid and α-Alkoxy Acid Derivatives via Cationic Intermediates. Eur. J. Org. Chem. 2003, 2003, 2519–2529. [Google Scholar] [CrossRef]
  87. Heimgartner, H.; Braun, K.; Linden, A. Synthesis and conformational analysis of pentapeptides containing enantiomerically pure 2,2-disubstituted glycines. Helv. Chim. Acta 2008, 91, 526–558. [Google Scholar] [CrossRef] [Green Version]
  88. Ohfune, Y.; Shinada, T. Enantio- and Diastereoselective Construction of α,α-Disubstituted α-Amino Acids for the Synthesis of Biologically Active Compounds. Eur. J. Org. Chem. 2005, 2005, 5127–5143. [Google Scholar] [CrossRef]
  89. Mazurkiewicz, R.; Kuźnik, A. A new convenient synthesis of N-acyl-2-(dimethoxyphosphoryl)glycinates. Tetrahedron Lett. 2006, 47, 3439–3442. [Google Scholar] [CrossRef]
  90. Kobayashi, K.; Tanaka, K.; Kogen, H. Recent topics of the natural product synthesis by Horner–Wadsworth–Emmons reaction. Tetrahedron Lett. 2018, 59, 568–582. [Google Scholar] [CrossRef]
  91. Mazurkiewicz, R.; Kuźnik, A.; Grymel, M.; Październiok-Holewa, A. α-Amino acid derivatives with a Cα-P bond in organic synthesis. Arkivoc 2007, 6, 193–216. [Google Scholar] [CrossRef]
  92. Pfefferkorn, J.A.; Nugent, R.A.; Gross, R.J.; Greene, M.L.; Mitchell, M.A.; Reding, M.T.; Funk, L.A.; Anderson, R.; Wells, P.A.; Shelly, J.A.; et al. Inhibitors of HCV NS5B polymerase. Part 2: Evaluation of the northern region of (2Z)-2-benzoylamino-3-(4-phenoxy-phenyl)-acrylic acid. Bioorg. Med. Chem. Lett. 2005, 15, 2812–2818. [Google Scholar] [CrossRef] [PubMed]
  93. Shangguan, N.; Joullié, M.M. Total synthesis of isoroquefortine E and phenylahistin. Tetrahedron Lett. 2009, 50, 6755–6757. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  94. Wang, W.; Xiong, C.; Zhang, J.; Hruby, V.J. Practical, asymmetric synthesis of aromatic-substituted bulky and hydrophobic tryptophan and phenylalanine derivatives. Tetrahedron 2002, 58, 3101–3110. [Google Scholar] [CrossRef]
  95. Cativiela, C.; Diaz de Villegas, M.D.; Gálvez, J.A.; Su, G. Horner-Wadsworth-Emmons reaction for the synthesis of unusual alpha,beta-didehydroamino acids with a chiral axis. Arkivoc 2004, 4, 59–66. [Google Scholar] [CrossRef] [Green Version]
  96. Aguado, G.P.; Moglioni, A.G.; Ortuño, R.M. Enantiodivergent synthesis of cyclobutyl-(Z)-α,β-dehydro-α-amino acid derivatives from (−)-cis-pinononic acid. Tetrahedron Asymmetry 2003, 14, 217–223. [Google Scholar] [CrossRef]
  97. Etayo, P.; Vidal-Ferran, A. Rhodium-catalysed asymmetric hydrogenation as a valuable synthetic tool for the preparation of chiral drugs. Chem. Soc. Rev. 2013, 42, 728–754. [Google Scholar] [CrossRef] [PubMed]
  98. Adamczyk, M.; Akireddy, S.R.; Reddy, R.E. Nonproteinogenic amino acids: An efficient asymmetric synthesis of (S)-(−)-acromelobic acid and (S)-(−)-acromelobinic acid. Tetrahedron 2002, 58, 6951–6963. [Google Scholar] [CrossRef]
  99. Blaskovich, M.A. Handbook on Syntheses of Amino Acids, General Routes to Amino Acids; American Chemical Society & Oxford University Press: New York, NY, USA, 2010. [Google Scholar]
  100. Yasuno, Y.; Mizutani, I.; Sueuchi, Y.; Wakabayashi, Y.; Yasuo, N.; Shimamoto, K.; Shinada, T. Catalytic Asymmetric Hydrogenation of Dehydroamino Acid Esters with Biscarbamate Protection and Its Application to the Synthesis of xCT Inhibitors. Chem. Eur. J. 2019, 25, 5145–5148. [Google Scholar] [CrossRef]
  101. Adamek, J.; Mrowiec-Białon, J.; Październiok-Holewa, A.; Mazurkiewicz, R. Thermogravimetrical investigations of the dealkoxycarbonylation of N-acyl-α-triphenylphosphonioglycinates. Thermochim. Acta 2011, 512, 22–27. [Google Scholar] [CrossRef]
  102. Gorewoda, T.; Mazurkiewicz, R.; Simka, W.; Mlostoń, G.; Schroeder, G.; Kubicki, M.; Kuźnik, N. 3-Triphenylphosphonio-2,5-piperazinediones as new chiral glycine cation equivalents. Tetrahedron Asymmetry 2011, 22, 823–833. [Google Scholar] [CrossRef]
Molecules 27 01562 sch001 550
Scheme 1. The α-amidoalkylation reaction.
Scheme 1. The α-amidoalkylation reaction.
Molecules 27 01562 sch001
Molecules 27 01562 g001 550
Figure 1. Areas of potential structural modifications within phosphonium precursors of α-amidoalkylating agents.
Figure 1. Areas of potential structural modifications within phosphonium precursors of α-amidoalkylating agents.
Molecules 27 01562 g001
Molecules 27 01562 sch002 550
Scheme 2. Classification and reactivity of 1-aminoalkylphosphonium derivatives.
Scheme 2. Classification and reactivity of 1-aminoalkylphosphonium derivatives.
Molecules 27 01562 sch002
Molecules 27 01562 g002 550
Figure 2. General structure of 1-(N-acylamino)alkylphosphonium salts 4.
Figure 2. General structure of 1-(N-acylamino)alkylphosphonium salts 4.
Molecules 27 01562 g002
Molecules 27 01562 sch003 550
Scheme 3. Methods for the synthesis of 1-(N-acylamino)methyltriphenylphosphonium salts 4a.
Scheme 3. Methods for the synthesis of 1-(N-acylamino)methyltriphenylphosphonium salts 4a.
Molecules 27 01562 sch003
Molecules 27 01562 sch004 550
Scheme 4. Synthesis of 1-(N-acylamino)benzoylmethyltriphenylphosphonium chlorides 17.
Scheme 4. Synthesis of 1-(N-acylamino)benzoylmethyltriphenylphosphonium chlorides 17.
Molecules 27 01562 sch004
Molecules 27 01562 sch005 550
Scheme 5. Synthesis of 1-(N-acylamino)vinylphosphonium salts (AVPOSs) 22.
Scheme 5. Synthesis of 1-(N-acylamino)vinylphosphonium salts (AVPOSs) 22.
Molecules 27 01562 sch005
Molecules 27 01562 sch006 550
Scheme 6. Synthesis of 1-(N-acylamino)alkylphosphonium salts 4 from oxazolones.
Scheme 6. Synthesis of 1-(N-acylamino)alkylphosphonium salts 4 from oxazolones.
Molecules 27 01562 sch006
Molecules 27 01562 sch007 550
Scheme 7. Modern strategy in the synthesis of 1-(N-acylamino)alkylphosphonium salts 4; Method A–Synthesis based on the electrochemical alkoxylation; Method B–Non-electrochemical synthesis based on the one-pot, three components coupling.
Scheme 7. Modern strategy in the synthesis of 1-(N-acylamino)alkylphosphonium salts 4; Method A–Synthesis based on the electrochemical alkoxylation; Method B–Non-electrochemical synthesis based on the one-pot, three components coupling.
Molecules 27 01562 sch007
Molecules 27 01562 sch008 550
Scheme 8. Step-by-step procedure for the synthesis of N-protected aminomethylphosphonium salts 4a.
Scheme 8. Step-by-step procedure for the synthesis of N-protected aminomethylphosphonium salts 4a.
Molecules 27 01562 sch008
Molecules 27 01562 g003 550
Figure 3. Applications of 1-(N-acylamino)alkylphosphonium salts 4.
Figure 3. Applications of 1-(N-acylamino)alkylphosphonium salts 4.
Molecules 27 01562 g003
Molecules 27 01562 sch009 550
Scheme 9. 1-(N-acylamino)alkyltriarylphosphonium salts 4 as precursors of N-acylimines 2 and N-acyliminium-type cations 3.
Scheme 9. 1-(N-acylamino)alkyltriarylphosphonium salts 4 as precursors of N-acylimines 2 and N-acyliminium-type cations 3.
Molecules 27 01562 sch009
Molecules 27 01562 sch010 550
Scheme 10. Generation of N-acyliminium-type cations from 1-(N-acylamino)alkyltriarylphosphonium salts 4.
Scheme 10. Generation of N-acyliminium-type cations from 1-(N-acylamino)alkyltriarylphosphonium salts 4.
Molecules 27 01562 sch010
Molecules 27 01562 sch011 550
Scheme 11. Michaelis–Arbuzov-type reaction of 1-(N-acylamino)alkylphosphonium salts 4 with P-nucleophiles.
Scheme 11. Michaelis–Arbuzov-type reaction of 1-(N-acylamino)alkylphosphonium salts 4 with P-nucleophiles.
Molecules 27 01562 sch011
Molecules 27 01562 sch012 550
Scheme 12. Methods for the obtaining of enantiomerically enriched phosphorus analogs of α-amino acids 37 via 1-(N-acylamino)alkyltriphenylphosphonium salts 4 based on enzymatic kinetic resolution (Method A) or organocatalytic α-amidoalkylation of P-nucleophiles in PTC systems (Method B).
Scheme 12. Methods for the obtaining of enantiomerically enriched phosphorus analogs of α-amino acids 37 via 1-(N-acylamino)alkyltriphenylphosphonium salts 4 based on enzymatic kinetic resolution (Method A) or organocatalytic α-amidoalkylation of P-nucleophiles in PTC systems (Method B).
Molecules 27 01562 sch012
Molecules 27 01562 sch013 550
Scheme 13. Synthesis and applications of 1-(N-acylamino)-1-triphenylphosphoniumalkylphosphonates 42. Reagents and conditions: (A) R3R4POR (e.g., P(OEt)3, MeP(OEt)2, Ph2P(OMe), etc.), (i-Pr)2EtN, Ph3P+Me I−, 20–60 °C, 0.3–6 h; (B) KCN, 18–crown–6, 20 °C, 24 h; (C) (i-Pr)2EtN, 20 °C, 5 h; (D) MeC(O)CF3, K2CO3, 18-crown-6, 50 °C, 4 h.
Scheme 13. Synthesis and applications of 1-(N-acylamino)-1-triphenylphosphoniumalkylphosphonates 42. Reagents and conditions: (A) R3R4POR (e.g., P(OEt)3, MeP(OEt)2, Ph2P(OMe), etc.), (i-Pr)2EtN, Ph3P+Me I−, 20–60 °C, 0.3–6 h; (B) KCN, 18–crown–6, 20 °C, 24 h; (C) (i-Pr)2EtN, 20 °C, 5 h; (D) MeC(O)CF3, K2CO3, 18-crown-6, 50 °C, 4 h.
Molecules 27 01562 sch013
Molecules 27 01562 sch014 550
Scheme 14. Reactivity of 1-(N-acylamino)alkyltriarylphosphonium salts 4 with nucleophiles.
Scheme 14. Reactivity of 1-(N-acylamino)alkyltriarylphosphonium salts 4 with nucleophiles.
Molecules 27 01562 sch014
Molecules 27 01562 sch015 550
Scheme 15. The synthetic use of the transformation of N,O-acetals to N-[1-(benzotriazol-1-yl)alkyl]amides 50 or α-amido sulfones 51, 56 via phosphonium salts.
Scheme 15. The synthetic use of the transformation of N,O-acetals to N-[1-(benzotriazol-1-yl)alkyl]amides 50 or α-amido sulfones 51, 56 via phosphonium salts.
Molecules 27 01562 sch015
Molecules 27 01562 sch016 550
Scheme 16. Conditions and yields for reactions of 1-(N-acylamino)alkyltriarylphosphonium salts 4 with 1,3-dicarbonyl compounds (A) or 1-morpholinocyclohexene (B).
Scheme 16. Conditions and yields for reactions of 1-(N-acylamino)alkyltriarylphosphonium salts 4 with 1,3-dicarbonyl compounds (A) or 1-morpholinocyclohexene (B).
Molecules 27 01562 sch016
Molecules 27 01562 sch017 550
Scheme 17. Reaction of 1-(N-acylamino)alkyltriarylphosphonium salts 4 with aromatic compounds: (A) synthetic routes, (B) plausible mechanism.
Scheme 17. Reaction of 1-(N-acylamino)alkyltriarylphosphonium salts 4 with aromatic compounds: (A) synthetic routes, (B) plausible mechanism.
Molecules 27 01562 sch017
Molecules 27 01562 sch018 550
Scheme 18. Reaction of 1-(N-acylamino)alkyltriarylphosphonium salts 4 with silyl enolates—(A) conditions and yields, (B) plausible mechanism.
Scheme 18. Reaction of 1-(N-acylamino)alkyltriarylphosphonium salts 4 with silyl enolates—(A) conditions and yields, (B) plausible mechanism.
Molecules 27 01562 sch018
Molecules 27 01562 sch019 550
Scheme 19. Synthesis of imidoyl chlorides 71 and their further transformations.
Scheme 19. Synthesis of imidoyl chlorides 71 and their further transformations.
Molecules 27 01562 sch019
Molecules 27 01562 g004 550
Figure 4. General structure of 1-imidoalkylphosphonium salts 79.
Figure 4. General structure of 1-imidoalkylphosphonium salts 79.
Molecules 27 01562 g004
Molecules 27 01562 sch020 550
Scheme 20. Three-step synthesis of 1-imidoalkylphosphonium salts 79 from amino acids.
Scheme 20. Three-step synthesis of 1-imidoalkylphosphonium salts 79 from amino acids.
Molecules 27 01562 sch020
Molecules 27 01562 sch021 550
Scheme 21. Three-component coupling of aldehydes, imides, and triarylphosphonium salts in the synthesis of 1-imidoalkylphosphonium salts 79.
Scheme 21. Three-component coupling of aldehydes, imides, and triarylphosphonium salts in the synthesis of 1-imidoalkylphosphonium salts 79.
Molecules 27 01562 sch021
Molecules 27 01562 sch022 550
Scheme 22. Step-by-step method for the synthesis of 1-imidoalkylphosphonium salts 79 from imides.
Scheme 22. Step-by-step method for the synthesis of 1-imidoalkylphosphonium salts 79 from imides.
Molecules 27 01562 sch022
Molecules 27 01562 g005 550
Figure 5. Applications of 1-imidoalkylphosphonium salts 79.
Figure 5. Applications of 1-imidoalkylphosphonium salts 79.
Molecules 27 01562 g005
Molecules 27 01562 sch023 550
Scheme 23. Friedel–Crafts-type reaction of 1-imidoalkylphosphonium salts 79 with various aromatic compounds–conditions and yields (MW–microvawe assisted reaction).
Scheme 23. Friedel–Crafts-type reaction of 1-imidoalkylphosphonium salts 79 with various aromatic compounds–conditions and yields (MW–microvawe assisted reaction).
Molecules 27 01562 sch023
Molecules 27 01562 sch024 550
Scheme 24. Unusual course of the reaction of 1-imidoalkylphosphonium salt 79-CF3 with a highly activated aromatic system–1,3,5-trimethoxybenzene.
Scheme 24. Unusual course of the reaction of 1-imidoalkylphosphonium salt 79-CF3 with a highly activated aromatic system–1,3,5-trimethoxybenzene.
Molecules 27 01562 sch024
Molecules 27 01562 sch025 550
Scheme 25. Michaelis–Arbuzov-type reaction of 1-imidoalkylphosphonium salts 79 with selected phosphorus nucleophiles.
Scheme 25. Michaelis–Arbuzov-type reaction of 1-imidoalkylphosphonium salts 79 with selected phosphorus nucleophiles.
Molecules 27 01562 sch025
Molecules 27 01562 g006 550
Figure 6. General structure of N-acyl-1-phosphonio-α-amino acid esters 91.
Figure 6. General structure of N-acyl-1-phosphonio-α-amino acid esters 91.
Molecules 27 01562 g006
Molecules 27 01562 sch026 550
Scheme 26. Method for the synthesis of N-acyl-1-triphenylphosphonioglycinate bromides 91 from glycine derivatives 92 via 1-bromoglycinates 93.
Scheme 26. Method for the synthesis of N-acyl-1-triphenylphosphonioglycinate bromides 91 from glycine derivatives 92 via 1-bromoglycinates 93.
Molecules 27 01562 sch026
Molecules 27 01562 sch027 550
Scheme 27. Synthesis of N-acyl-1-triphenylphosphonio-α-amino acid esters 91 via phosphoranylidene-5(4H)-oxazolones 24.
Scheme 27. Synthesis of N-acyl-1-triphenylphosphonio-α-amino acid esters 91 via phosphoranylidene-5(4H)-oxazolones 24.
Molecules 27 01562 sch027
Molecules 27 01562 sch028 550
Scheme 28. Methodology for the synthesis of N-acyl-1-triphenylphosphonioglycinates 91 via α-hydroxyglycinates. Reagents and conditions: Procedure A: Ph3P·Br2, Et3N, Ph3P, DCM, rt; Procedure B: DCC, Ph3P·HBF4, Ph3P, DCM, rt; Procedure C: DEAD (diethyl azodicarboxylate), Ph3P·HBF4, Ph3P, THF, rt.
Scheme 28. Methodology for the synthesis of N-acyl-1-triphenylphosphonioglycinates 91 via α-hydroxyglycinates. Reagents and conditions: Procedure A: Ph3P·Br2, Et3N, Ph3P, DCM, rt; Procedure B: DCC, Ph3P·HBF4, Ph3P, DCM, rt; Procedure C: DEAD (diethyl azodicarboxylate), Ph3P·HBF4, Ph3P, THF, rt.
Molecules 27 01562 sch028
Molecules 27 01562 g007 550
Figure 7. Applications of N-acyl-1-phosphonio-α-amino acid esters 91.
Figure 7. Applications of N-acyl-1-phosphonio-α-amino acid esters 91.
Molecules 27 01562 g007
Molecules 27 01562 sch029 550
Scheme 29. Various pathways for synthetic applications of N-acyl-1-triphenylphosphonio-α-amino acid esters 91 in the presence of a base (Et3N or DBU).
Scheme 29. Various pathways for synthetic applications of N-acyl-1-triphenylphosphonio-α-amino acid esters 91 in the presence of a base (Et3N or DBU).
Molecules 27 01562 sch029
Molecules 27 01562 sch030 550
Scheme 30. Synthetic applications of N-acyl-1-triphenylphosphonio-α-amino acid esters 91 in reactions with heteronucleophiles.
Scheme 30. Synthetic applications of N-acyl-1-triphenylphosphonio-α-amino acid esters 91 in reactions with heteronucleophiles.
Molecules 27 01562 sch030
Molecules 27 01562 sch031 550
Scheme 31. Synthetic applications of N-acyl-1-triphenylphosphonio-α-amino acid esters 91 in reactions with C-nucleophiles.
Scheme 31. Synthetic applications of N-acyl-1-triphenylphosphonio-α-amino acid esters 91 in reactions with C-nucleophiles.
Molecules 27 01562 sch031
Molecules 27 01562 sch032 550
Scheme 32. Transformation of N-acyl-1-triphenylphosphonioglycinate tetrafluoroborates 91 into N-acyl-α-(dimethoxyphosphoryl)glycinates 108 and selected examples of their further use in the synthesis of biologically active compounds.
Scheme 32. Transformation of N-acyl-1-triphenylphosphonioglycinate tetrafluoroborates 91 into N-acyl-α-(dimethoxyphosphoryl)glycinates 108 and selected examples of their further use in the synthesis of biologically active compounds.
Molecules 27 01562 sch032
Molecules 27 01562 sch033 550
Scheme 33. Thermal stability of N-acyl-1-triphenylphosphonio-α-amino acid esters 91.
Scheme 33. Thermal stability of N-acyl-1-triphenylphosphonio-α-amino acid esters 91.
Molecules 27 01562 sch033
Molecules 27 01562 sch034 550
Scheme 34. Synthetic use of 3-triphenylphosphonio-2,5-piperazinedione 111, 114-chiral glycine cation equivalents.
Scheme 34. Synthetic use of 3-triphenylphosphonio-2,5-piperazinedione 111, 114-chiral glycine cation equivalents.
Molecules 27 01562 sch034
Molecules 27 01562 g008 550
Figure 8. 1-Aminoalkylphosphonium derivatives—new challenges.
Figure 8. 1-Aminoalkylphosphonium derivatives—new challenges.
Molecules 27 01562 g008
Table
Table 1. Summary of characteristics for the most important precursors of α-amidoalkylating agents 1.
Table 1. Summary of characteristics for the most important precursors of α-amidoalkylating agents 1.
Structure of PrecursorSummary of CharacteristicsExamples of Use in α-Amidoalkylation
(Selected Research or Review Literature) a
Molecules 27 01562 i001limited structural diversity, limited reactivity, parent compounds for the other α-amidoalkylating agents, activation with acidic catalysts, synthesis from amides (or imides) and aldehydes (mostly in situ)—only N-hydoxymethylamides (or -imides) can be easily isolated[3,4,6,7,8,9,10,11,12]
Molecules 27 01562 i002limited reactivity, high structural diversity, activation with acidic catalysts, main synthesis methods based on electrochemical alkoxylation[5,6,7,8,9,12,13,14]
Molecules 27 01562 i003high reactivity, rather low yields in α-amidoalkylation reactions (lots of by-products), difficulties in the preparation, purification and storage[6,7,8,9,12]
Molecules 27 01562 i004high reactivity (good leaving group), high structural diversity, activation with acidic catalysts, easy to use and storage, diverse methods of synthesis, broad scope of application [8,9,12,16,17,18,19]
Molecules 27 01562 i005high reactivity (good leaving group), high structural diversity, activation with acidic catalysts, easy to use and storage, diverse methods of synthesis, broad scope of application, currently the most popular and convenient[8,9,12,20,21,22,23]
a Selected examples aimed at showing the most recent interest in α-amidoalkylation reactions.
Table
Table 2. Conditions and yields for the synthesis of phthalimidomethylphosphonium salts 79.
Table 2. Conditions and yields for the synthesis of phthalimidomethylphosphonium salts 79.
Molecules 27 01562 i006
EntrySubstrate 80SolventConditionsYield of 79, %Refs.
X
1(Me3N)+ I-methanolreflux, 4 h58[70]
2Clbenzenereflux, 2 h-[70]
3Bracetonereflux, 3 min80[24]
4Brbenzenereflux, 22 h68[67,71] a
5Brtoluenereflux, 24 h-[72]
a Compound 79 (X = Br) is also formed as a by-product in the reaction with Pd(PPh3)4 (rt, benzene).
Table
Table 3. Application of phthalimidomethyltriphenylphosphonium bromide as ylide precursors.
Table 3. Application of phthalimidomethyltriphenylphosphonium bromide as ylide precursors.
Molecules 27 01562 i007
Phosphonium Salt 79Carbonyl ComponentsConditionsIntermediate CompoundTargeted Compound
Molecules 27 01562 i008 Molecules 27 01562 i009KHMDS, THF, 0 °C→RT, 86% Molecules 27 01562 i01085
Molecules 27 01562 i011KHMDS, THF, 0 °C→RT, 77% Molecules 27 01562 i01286
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Adamek, J.; Grymel, M.; Kuźnik, A.; Październiok-Holewa, A. 1-Aminoalkylphosphonium Derivatives: Smart Synthetic Equivalents of N-Acyliminium-Type Cations, and Maybe Something More: A Review. Molecules 2022, 27, 1562. https://doi.org/10.3390/molecules27051562

AMA Style

Adamek J, Grymel M, Kuźnik A, Październiok-Holewa A. 1-Aminoalkylphosphonium Derivatives: Smart Synthetic Equivalents of N-Acyliminium-Type Cations, and Maybe Something More: A Review. Molecules. 2022; 27(5):1562. https://doi.org/10.3390/molecules27051562

Chicago/Turabian Style

Adamek, Jakub, Mirosława Grymel, Anna Kuźnik, and Agnieszka Październiok-Holewa. 2022. "1-Aminoalkylphosphonium Derivatives: Smart Synthetic Equivalents of N-Acyliminium-Type Cations, and Maybe Something More: A Review" Molecules 27, no. 5: 1562. https://doi.org/10.3390/molecules27051562

Article Metrics

Back to TopTop