Synthesis of Heteroaromatic Compounds

doi:10.3390/books978-3-0365-7562-9

dc.contributor.editor	Sloop, Joseph
dc.date.accessioned	2023-06-23T09:44:45Z
dc.date.available	2023-06-23T09:44:45Z
dc.date.issued	2023
dc.identifier	ONIX_20230623_9783036575636_45
dc.identifier.uri	https://directory.doabooks.org/handle/20.500.12854/100813
dc.description.abstract	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.
dc.language	English
dc.subject.classification	thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general	en_US
dc.subject.classification	thema EDItEUR::P Mathematics and Science::PN Chemistry	en_US
dc.subject.classification	thema EDItEUR::P Mathematics and Science::PN Chemistry::PNN Organic chemistry	en_US
dc.subject.other	heteroaromatics
dc.subject.other	C-H bond functionalization
dc.subject.other	oxidative cyclization
dc.subject.other	cross-coupling
dc.subject.other	amination
dc.subject.other	triazoles
dc.subject.other	palladium
dc.subject.other	carbene ligands
dc.subject.other	heterocycles
dc.subject.other	nitrogen-containing heterocycles
dc.subject.other	synthesis
dc.subject.other	antiviral agents
dc.subject.other	viruses
dc.subject.other	COVID-19
dc.subject.other	inhibition
dc.subject.other	Mpro inhibitors
dc.subject.other	drug design and synthesis
dc.subject.other	structure-activity relationships (SAR)
dc.subject.other	s-tetrazine
dc.subject.other	4H-1,2,4-triazole
dc.subject.other	pinner reaction
dc.subject.other	1,2,3-triazole
dc.subject.other	fused 1,2,3-triazole
dc.subject.other	1,2,3-triazolo[4,5-b]pyrazine
dc.subject.other	1,2,3-triazolo[4,5-c]pyridazine
dc.subject.other	1,2,3-triazolo[4,5-d]pyridazine
dc.subject.other	1,2,3-triazolo[1,5-a]pyrazine
dc.subject.other	1,2,3-triazolo[1,5-b]pyridazine
dc.subject.other	triazolopyrazine
dc.subject.other	triazolopyridazine
dc.subject.other	practical applications
dc.subject.other	spiro π-conjugated compound
dc.subject.other	chiral compound
dc.subject.other	thiophene
dc.subject.other	furan
dc.subject.other	pyrrole
dc.subject.other	nucleophilic aromatic substitution
dc.subject.other	circular dichroism
dc.subject.other	circularly polarized luminescence
dc.subject.other	pyridines
dc.subject.other	1,3,4-thiadiazoles
dc.subject.other	1,3-thiazoles
dc.subject.other	hydrazonoyl halides
dc.subject.other	molecular docking
dc.subject.other	anticancer activity
dc.subject.other	1,3,4-oxadiazoles
dc.subject.other	organic ligands
dc.subject.other	substitution
dc.subject.other	diisopropyl iminodiacetate
dc.subject.other	pyrimidine
dc.subject.other	benzimidazole
dc.subject.other	aza-Diels–Alder reaction
dc.subject.other	Povarov reaction
dc.subject.other	oxidation
dc.subject.other	fluorescence
dc.subject.other	aggregation-induced emission
dc.subject.other	mechanochromic properties
dc.subject.other	heterocycle
dc.subject.other	natural product
dc.subject.other	nicotinic acid
dc.subject.other	fungicidal activity
dc.subject.other	4-pyrone
dc.subject.other	DMF-DMA
dc.subject.other	enamination
dc.subject.other	cycloaddition
dc.subject.other	merocyanine
dc.subject.other	1,6-conjugate addition
dc.subject.other	solvatochromism
dc.subject.other	fluorophore
dc.subject.other	acetylcoumarin
dc.subject.other	thiazoles
dc.subject.other	VEGFR-2
dc.subject.other	polyfluoroflavones
dc.subject.other	1H-1,2,4-triazole
dc.subject.other	imidazole
dc.subject.other	regioselectivity
dc.subject.other	azolyl-substituted flavones
dc.subject.other	photoluminescence
dc.subject.other	4-pyridone
dc.subject.other	oxazinone
dc.subject.other	ring-opening
dc.subject.other	aldehyde-lactol tautomerism
dc.subject.other	ammonium acetate
dc.subject.other	diazirine
dc.subject.other	medicinal chemistry
dc.subject.other	photoaffinity labeling
dc.subject.other	metathesis
dc.subject.other	carboaromatics
dc.subject.other	4,5-dihydro-5-oxo-pyrazolo[1,5-a]thieno[2,3-c]pyrimidines
dc.subject.other	novel scaffold
dc.subject.other	molecular dynamic studies
dc.subject.other	proximity frequencies (PF)
dc.subject.other	GABAA receptor subtype
dc.subject.other	GABAA receptor ligands
dc.subject.other	antibacterial
dc.subject.other	anticancer
dc.subject.other	antifibrotic
dc.subject.other	antifungal
dc.subject.other	antimicrobial
dc.subject.other	antiviral
dc.subject.other	appel salt
dc.subject.other	1,2,3-dithiazole
dc.subject.other	disulfide bridge
dc.subject.other	herbicidal
dc.subject.other	chalcone
dc.subject.other	heteroaromatic
dc.subject.other	hybrid chalcone
dc.subject.other	n/a
dc.title	Synthesis of Heteroaromatic Compounds
dc.type	book
oapen.identifier.doi	10.3390/books978-3-0365-7562-9
oapen.relation.isPublishedBy	46cabcaa-dd94-4bfe-87b4-55023c1b36d0
oapen.relation.isbn	9783036575636
oapen.relation.isbn	9783036575629
oapen.pages	446
oapen.place.publication	Basel

Files in this item

Files	Size	Format	View
There are no files associated with this item.

This item appears in the following Collection(s)

Imported or submitted locally

Show simple item record

Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0/