Modern Strategies for Heterocycle Synthesis

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-couplin...

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Detalles Bibliográficos
Otros Autores:	Favi, Gianfranco (Editor)
Formato:	Libro electrónico
Idioma:	Inglés
Publicado:	Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute 2021
Materias:	Medicine amine nucleophiles alkynoic acids cascade reaction gold catalysis fused N-heterocycles solid-phase synthesis ketone traceless synthesis natural products enol ethers photocatalysis photoredox visible-light-induced catalysis photoredox cyclization organic dyes heterocycles dihydrocoumarins synthesis 3-trifluoroacetyl coumarins phenols antifungal activities terpyridines 3,2':6',3"-terpyridine cyclohexanol derivative condensation heterocyclic 1,2,3-triazol triazolylmethyl phosphinate triazolylmethyl phosphate copper-catalyzed azide-alkyne cycloaddition click reaction azides cinnolines triazoles CuAAC alkynes cycloalkynes Richter cyclization Suzuki coupling fluorescence cytotoxicity coumarin pyrazolo[3,4-b]pyridine silica sulfuric acid 2H-pyran valence isomerism 1-oxa-triene dienone oxa-electrocyclization Knoevenagel propargyl Claisen cycloisomerization asymmetric dimeric β-carboline acylhydrazone group cytotoxic antitumor structure-activity relationship γ-lactam pyrrolidones multicomponent reactions organocatalysis pyridine CF3CO-acetylenes 1,3-oxazines fluorinated heterocycles saturated oxygen heterocycles cyclic ethers total synthesis multicomponent reaction α-halohydrazones Staudinger reaction aza-Wittig 1H-imidazole-2(3H)-thione 2H-imidazo[2,1-b][1,3,4]thiadiazine purine nucleobase aromatic substitution arylation fluoroalcohol α-chloroglycinates 5-acylamino-1,3-thiazoles Hantzsch reaction TMSBr propargylic alcohols cascade cyclization 4-bromo quinolines synthesis of benzofurans intra-molecular approach inter-molecular approach
Ver en Biblioteca Universitat Ramon Llull:	https://discovery.url.edu/permalink/34CSUC_URL/1im36ta/alma991009654568906719