Reprint
Synthesis of Heteroaromatic Compounds
Edited by
May 2023
446 pages
- ISBN978-3-0365-7563-6 (Hardback)
- ISBN978-3-0365-7562-9 (PDF)
This book is a reprint of the Special Issue Synthesis of Heteroaromatic Compounds that was published in
Chemistry & Materials Science
Medicine & Pharmacology
Summary
This Special Issue, entitled the “Synthesis of Heteroaromatic Compounds”, is an outstanding collection of fourteen original research papers and six review articles that discuss the advances made in both conventional and green preparatory methods, as well as the properties and applications of heteroaromatic molecules in industrial and medicinal chemistry areas of study.The collected works featured herein collate contributions from a truly international and diverse array of ninety experts in the fields of heteroaromatic compound synthesis, QSAR studies, computational chemistry and molecular docking, as well as bioactivity studies.
Format
- Hardback
License
© 2022 by the authors; CC BY-NC-ND license
Keywords
heteroaromatics; C-H bond functionalization; oxidative cyclization; cross-coupling; amination; triazoles; palladium; carbene ligands; heterocycles; nitrogen-containing heterocycles; synthesis; antiviral agents; viruses; COVID-19; inhibition; COVID-19; Mpro inhibitors; drug design and synthesis; structure-activity relationships (SAR); s-tetrazine; 4H-1,2,4-triazole; pinner reaction; synthesis; 1,2,3-triazole; fused 1,2,3-triazole; 1,2,3-triazolo[4,5-b]pyrazine; 1,2,3-triazolo[4,5-c]pyridazine; 1,2,3-triazolo[4,5-d]pyridazine; 1,2,3-triazolo[1,5-a]pyrazine; 1,2,3-triazolo[1,5-b]pyridazine; triazolopyrazine; triazolopyridazine; practical applications; spiro π-conjugated compound; chiral compound; thiophene; furan; pyrrole; nucleophilic aromatic substitution; circular dichroism; circularly polarized luminescence; pyridines; 1,3,4-thiadiazoles; 1,3-thiazoles; hydrazonoyl halides; molecular docking; anticancer activity; 1,3,4-oxadiazoles; organic ligands; heterocycles; substitution; diisopropyl iminodiacetate; pyrimidine; benzimidazole; aza-Diels–Alder reaction; Povarov reaction; oxidation; fluorescence; aggregation-induced emission; mechanochromic properties; heterocycle; natural product; nicotinic acid; thiophene; fungicidal activity; 4-pyrone; DMF-DMA; enamination; cycloaddition; merocyanine; 1,6-conjugate addition; solvatochromism; fluorophore; acetylcoumarin; hydrazonoyl halides; thiazoles; molecular docking; VEGFR-2; polyfluoroflavones; 1H-1,2,4-triazole; imidazole; nucleophilic aromatic substitution; regioselectivity; azolyl-substituted flavones; photoluminescence; 4-pyridone; oxazinone; ring-opening; benzimidazole; aldehyde-lactol tautomerism; ammonium acetate; diazirine; heteroaromatics; medicinal chemistry; photoaffinity labeling; metathesis; heteroaromatics; carboaromatics; 4,5-dihydro-5-oxo-pyrazolo[1,5-a]thieno[2,3-c]pyrimidines; novel scaffold; thiophene; molecular dynamic studies; proximity frequencies (PF); GABAA receptor subtype; GABAA receptor ligands; antibacterial; anticancer; antifibrotic; antifungal; antimicrobial; antiviral; appel salt; 1,2,3-dithiazole; disulfide bridge; herbicidal; chalcone; heteroaromatic; hybrid chalcone; n/a