Synthesis of Heteroaromatic Compounds

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...

Full description

Saved in:
Bibliographic Details
Other Authors: Sloop, Joseph (Editor)
Format: Electronic Book Chapter
Language:English
Published: Basel MDPI - Multidisciplinary Digital Publishing Institute 2023
Subjects:
n/a
Online Access:DOAB: download the publication
DOAB: description of the publication
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000naaaa2200000uu 4500
001 doab_20_500_12854_100813
005 20230623
003 oapen
006 m o d
007 cr|mn|---annan
008 20230623s2023 xx |||||o ||| 0|eng d
020 |a books978-3-0365-7562-9 
020 |a 9783036575636 
020 |a 9783036575629 
040 |a oapen  |c oapen 
024 7 |a 10.3390/books978-3-0365-7562-9  |c doi 
041 0 |a eng 
042 |a dc 
072 7 |a GP  |2 bicssc 
072 7 |a PN  |2 bicssc 
072 7 |a PNN  |2 bicssc 
100 1 |a Sloop, Joseph  |4 edt 
700 1 |a Sloop, Joseph  |4 oth 
245 1 0 |a Synthesis of Heteroaromatic Compounds 
260 |a Basel  |b MDPI - Multidisciplinary Digital Publishing Institute  |c 2023 
300 |a 1 electronic resource (446 p.) 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
506 0 |a Open Access  |2 star  |f Unrestricted online access 
520 |a 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. 
540 |a Creative Commons  |f https://creativecommons.org/licenses/by/4.0/  |2 cc  |4 https://creativecommons.org/licenses/by/4.0/ 
546 |a English 
650 7 |a Research & information: general  |2 bicssc 
650 7 |a Chemistry  |2 bicssc 
650 7 |a Organic chemistry  |2 bicssc 
653 |a heteroaromatics 
653 |a C-H bond functionalization 
653 |a oxidative cyclization 
653 |a cross-coupling 
653 |a amination 
653 |a triazoles 
653 |a palladium 
653 |a carbene ligands 
653 |a heterocycles 
653 |a nitrogen-containing heterocycles 
653 |a synthesis 
653 |a antiviral agents 
653 |a viruses 
653 |a COVID-19 
653 |a inhibition 
653 |a Mpro inhibitors 
653 |a drug design and synthesis 
653 |a structure-activity relationships (SAR) 
653 |a s-tetrazine 
653 |a 4H-1,2,4-triazole 
653 |a pinner reaction 
653 |a 1,2,3-triazole 
653 |a fused 1,2,3-triazole 
653 |a 1,2,3-triazolo[4,5-b]pyrazine 
653 |a 1,2,3-triazolo[4,5-c]pyridazine 
653 |a 1,2,3-triazolo[4,5-d]pyridazine 
653 |a 1,2,3-triazolo[1,5-a]pyrazine 
653 |a 1,2,3-triazolo[1,5-b]pyridazine 
653 |a triazolopyrazine 
653 |a triazolopyridazine 
653 |a practical applications 
653 |a spiro π-conjugated compound 
653 |a chiral compound 
653 |a thiophene 
653 |a furan 
653 |a pyrrole 
653 |a nucleophilic aromatic substitution 
653 |a circular dichroism 
653 |a circularly polarized luminescence 
653 |a pyridines 
653 |a 1,3,4-thiadiazoles 
653 |a 1,3-thiazoles 
653 |a hydrazonoyl halides 
653 |a molecular docking 
653 |a anticancer activity 
653 |a 1,3,4-oxadiazoles 
653 |a organic ligands 
653 |a substitution 
653 |a diisopropyl iminodiacetate 
653 |a pyrimidine 
653 |a benzimidazole 
653 |a aza-Diels-Alder reaction 
653 |a Povarov reaction 
653 |a oxidation 
653 |a fluorescence 
653 |a aggregation-induced emission 
653 |a mechanochromic properties 
653 |a heterocycle 
653 |a natural product 
653 |a nicotinic acid 
653 |a fungicidal activity 
653 |a 4-pyrone 
653 |a DMF-DMA 
653 |a enamination 
653 |a cycloaddition 
653 |a merocyanine 
653 |a 1,6-conjugate addition 
653 |a solvatochromism 
653 |a fluorophore 
653 |a acetylcoumarin 
653 |a thiazoles 
653 |a VEGFR-2 
653 |a polyfluoroflavones 
653 |a 1H-1,2,4-triazole 
653 |a imidazole 
653 |a regioselectivity 
653 |a azolyl-substituted flavones 
653 |a photoluminescence 
653 |a 4-pyridone 
653 |a oxazinone 
653 |a ring-opening 
653 |a aldehyde-lactol tautomerism 
653 |a ammonium acetate 
653 |a diazirine 
653 |a medicinal chemistry 
653 |a photoaffinity labeling 
653 |a metathesis 
653 |a carboaromatics 
653 |a 4,5-dihydro-5-oxo-pyrazolo[1,5-a]thieno[2,3-c]pyrimidines 
653 |a novel scaffold 
653 |a molecular dynamic studies 
653 |a proximity frequencies (PF) 
653 |a GABAA receptor subtype 
653 |a GABAA receptor ligands 
653 |a antibacterial 
653 |a anticancer 
653 |a antifibrotic 
653 |a antifungal 
653 |a antimicrobial 
653 |a antiviral 
653 |a appel salt 
653 |a 1,2,3-dithiazole 
653 |a disulfide bridge 
653 |a herbicidal 
653 |a chalcone 
653 |a heteroaromatic 
653 |a hybrid chalcone 
653 |a n/a 
856 4 0 |a www.oapen.org  |u https://mdpi.com/books/pdfview/book/7276  |7 0  |z DOAB: download the publication 
856 4 0 |a www.oapen.org  |u https://directory.doabooks.org/handle/20.500.12854/100813  |7 0  |z DOAB: description of the publication