LEADER 05063nam 2201393z- 450 001 9910557409903321 005 20231214133337.0 035 $a(CKB)5400000000043577 035 $a(oapen)https://directory.doabooks.org/handle/20.500.12854/68487 035 $a(EXLCZ)995400000000043577 100 $a20202105d2021 |y 0 101 0 $aeng 135 $aurmn|---annan 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aModern Strategies for Heterocycle Synthesis 210 $aBasel, Switzerland$cMDPI - Multidisciplinary Digital Publishing Institute$d2021 215 $a1 electronic resource (372 p.) 311 $a3-0365-0340-4 311 $a3-0365-0341-2 330 $aHeterocycles 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. 606 $aMedicine$2bicssc 610 $aamine nucleophiles 610 $aalkynoic acids 610 $acascade reaction 610 $agold catalysis 610 $afused N-heterocycles 610 $asolid-phase synthesis 610 $aketone 610 $atraceless synthesis 610 $anatural products 610 $aenol ethers 610 $aphotocatalysis 610 $aphotoredox 610 $avisible-light-induced catalysis 610 $aphotoredox cyclization 610 $aorganic dyes 610 $aheterocycles 610 $adihydrocoumarins 610 $asynthesis 610 $a3-trifluoroacetyl coumarins 610 $aphenols 610 $aantifungal activities 610 $aterpyridines 610 $a3,2':6',3"-terpyridine 610 $acyclohexanol derivative 610 $acondensation 610 $aheterocyclic 610 $a1,2,3-triazol 610 $atriazolylmethyl phosphinate 610 $atriazolylmethyl phosphate 610 $acopper-catalyzed azide-alkyne cycloaddition 610 $aclick reaction 610 $aazides 610 $acinnolines 610 $atriazoles 610 $aCuAAC 610 $aalkynes 610 $acycloalkynes 610 $aRichter cyclization 610 $aSuzuki coupling 610 $afluorescence 610 $acytotoxicity 610 $acoumarin 610 $apyrazolo[3,4-b]pyridine 610 $asilica sulfuric acid 610 $a2H-pyran 610 $avalence isomerism 610 $a1-oxa-triene 610 $adienone 610 $aoxa-electrocyclization 610 $aKnoevenagel 610 $apropargyl Claisen 610 $acycloisomerization 610 $aasymmetric dimeric ?-carboline 610 $aacylhydrazone group 610 $acytotoxic 610 $aantitumor 610 $astructure-activity relationship 610 $a?-lactam 610 $apyrrolidones 610 $amulticomponent reactions 610 $aorganocatalysis 610 $apyridine 610 $aCF3CO-acetylenes 610 $a1,3-oxazines 610 $afluorinated heterocycles 610 $asaturated oxygen heterocycles 610 $acyclic ethers 610 $atotal synthesis 610 $amulticomponent reaction 610 $a?-halohydrazones 610 $aStaudinger reaction 610 $aaza-Wittig 610 $a1H-imidazole-2(3H)-thione 610 $a2H-imidazo[2,1-b][1,3,4]thiadiazine 610 $apurine 610 $anucleobase 610 $aaromatic substitution 610 $aarylation 610 $afluoroalcohol 610 $a?-chloroglycinates 610 $a5-acylamino-1,3-thiazoles 610 $aHantzsch reaction 610 $aTMSBr 610 $apropargylic alcohols 610 $acascade cyclization 610 $a4-bromo quinolines 610 $asynthesis of benzofurans 610 $aintra-molecular approach 610 $ainter-molecular approach 615 7$aMedicine 700 $aFavi$b Gianfranco$4edt$01314046 702 $aFavi$b Gianfranco$4oth 906 $aBOOK 912 $a9910557409903321 996 $aModern Strategies for Heterocycle Synthesis$93031622 997 $aUNINA