05098nam 2201417z- 450 991055740990332120210501(CKB)5400000000043577(oapen)https://directory.doabooks.org/handle/20.500.12854/68487(oapen)doab68487(EXLCZ)99540000000004357720202105d2021 |y 0engurmn|---annantxtrdacontentcrdamediacrrdacarrierModern Strategies for Heterocycle SynthesisBasel, SwitzerlandMDPI - Multidisciplinary Digital Publishing Institute20211 online resource (372 p.)3-0365-0340-4 3-0365-0341-2 Heterocycles feature widely in natural products, agrochemicals, pharmaceuticals and dyes, and their synthesis is of great interest to synthetic chemists in both academia and industry. The contributions of recent applications of new methodologies in C-H activation, photoredox chemistry, cross-coupling strategies, borrowing hydrogen catalysis, multicomponent and solvent-free reactions, regio- and stereoselective syntheses, as well as other new, attractive approaches for the construction of heterocyclic scaffolds are of great interest. This Special Issue is dedicated to featuring the latest research that is ongoing in the field of heterocyclic synthesis. It is expected that most submissions will focus on five- and six-membered oxygen and nitrogen-containing heterocycles, but structures incorporating other rings/heteroatoms will also be considered. Original research (communications, full papers and reviews) that discusses innovative methodologies for assembling heterocycles with potential application in materials, catalysis and medicine are therefore welcome.Medicinebicssc1-oxa-triene1,2,3-triazol1,3-oxazines1H-imidazole-2(3H)-thione2H-imidazo[2,1-b][1,3,4]thiadiazine2H-pyran3-trifluoroacetyl coumarins3,2':6',3"-terpyridine4-bromo quinolines5-acylamino-1,3-thiazolesacylhydrazone groupalkynesalkynoic acidsamine nucleophilesantifungal activitiesantitumoraromatic substitutionarylationasymmetric dimeric β-carbolineaza-Wittigazidescascade cyclizationcascade reactionCF3CO-acetylenescinnolinesclick reactioncondensationcopper-catalyzed azide-alkyne cycloadditioncoumarinCuAACcyclic etherscycloalkynescyclohexanol derivativecycloisomerizationcytotoxiccytotoxicitydienonedihydrocoumarinsenol ethersfluorescencefluorinated heterocyclesfluoroalcoholfused N-heterocyclesgold catalysisHantzsch reactionheterocyclesheterocyclicinter-molecular approachintra-molecular approachketoneKnoevenagelmulticomponent reactionmulticomponent reactionsn/anatural productsnucleobaseorganic dyesorganocatalysisoxa-electrocyclizationphenolsphotocatalysisphotoredoxphotoredox cyclizationpropargyl Claisenpropargylic alcoholspurinepyrazolo[3,4-b]pyridinepyridinepyrrolidonesRichter cyclizationsaturated oxygen heterocyclessilica sulfuric acidsolid-phase synthesisStaudinger reactionstructure-activity relationshipSuzuki couplingsynthesissynthesis of benzofuransterpyridinesTMSBrtotal synthesistraceless synthesistriazolestriazolylmethyl phosphatetriazolylmethyl phosphinatevalence isomerismvisible-light-induced catalysisα-chloroglycinatesα-halohydrazonesγ-lactamMedicineFavi Gianfrancoedt1314046Favi GianfrancoothBOOK9910557409903321Modern Strategies for Heterocycle Synthesis3031622UNINA