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C–H activation-annulation on the N-heterocyclic carbene platform

Ring-fused cationic N-heterocycles are an important class of organic compounds recognized to be of significant interest in diverse research areas including bioactivity, materials chemistry, supramolecular chemistry, etc. Toward the synthesis of such molecules, recently unique chemistry has been expl...

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Detalles Bibliográficos
Autores principales: Dutta, Champak, Choudhury, Joyanta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9084354/
https://www.ncbi.nlm.nih.gov/pubmed/35542736
http://dx.doi.org/10.1039/c8ra03799j
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author Dutta, Champak
Choudhury, Joyanta
author_facet Dutta, Champak
Choudhury, Joyanta
author_sort Dutta, Champak
collection PubMed
description Ring-fused cationic N-heterocycles are an important class of organic compounds recognized to be of significant interest in diverse research areas including bioactivity, materials chemistry, supramolecular chemistry, etc. Toward the synthesis of such molecules, recently unique chemistry has been explored utilizing a novel conjugative action of NHC ligands as a functionalizable directing group in rhodium(iii)-catalyzed aromatic/heteroaromatic/non-aromatic C–H activation and subsequent annulation of various imidazolium salts with internal alkynes. This review highlights the initial development and underscores the potential of this chemistry.
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spelling pubmed-90843542022-05-09 C–H activation-annulation on the N-heterocyclic carbene platform Dutta, Champak Choudhury, Joyanta RSC Adv Chemistry Ring-fused cationic N-heterocycles are an important class of organic compounds recognized to be of significant interest in diverse research areas including bioactivity, materials chemistry, supramolecular chemistry, etc. Toward the synthesis of such molecules, recently unique chemistry has been explored utilizing a novel conjugative action of NHC ligands as a functionalizable directing group in rhodium(iii)-catalyzed aromatic/heteroaromatic/non-aromatic C–H activation and subsequent annulation of various imidazolium salts with internal alkynes. This review highlights the initial development and underscores the potential of this chemistry. The Royal Society of Chemistry 2018-08-06 /pmc/articles/PMC9084354/ /pubmed/35542736 http://dx.doi.org/10.1039/c8ra03799j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Dutta, Champak
Choudhury, Joyanta
C–H activation-annulation on the N-heterocyclic carbene platform
title C–H activation-annulation on the N-heterocyclic carbene platform
title_full C–H activation-annulation on the N-heterocyclic carbene platform
title_fullStr C–H activation-annulation on the N-heterocyclic carbene platform
title_full_unstemmed C–H activation-annulation on the N-heterocyclic carbene platform
title_short C–H activation-annulation on the N-heterocyclic carbene platform
title_sort c–h activation-annulation on the n-heterocyclic carbene platform
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9084354/
https://www.ncbi.nlm.nih.gov/pubmed/35542736
http://dx.doi.org/10.1039/c8ra03799j
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