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Light opens a new window for N-heterocyclic carbene catalysis

N-Heterocyclic carbenes (NHCs) are efficient Lewis basic catalysts for the umpolung of various polarized unsaturated compounds usually including aldehydes, imines, acyl chlorides and activated esters. NHC catalysis involving electron pair transfer steps has been extensively studied; however, NHC cat...

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Autores principales: Liu, Jing, Xing, Xiao-Ning, Huang, Jin-Hai, Lu, Liang-Qiu, Xiao, Wen-Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162372/
https://www.ncbi.nlm.nih.gov/pubmed/34094315
http://dx.doi.org/10.1039/d0sc03595e
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author Liu, Jing
Xing, Xiao-Ning
Huang, Jin-Hai
Lu, Liang-Qiu
Xiao, Wen-Jing
author_facet Liu, Jing
Xing, Xiao-Ning
Huang, Jin-Hai
Lu, Liang-Qiu
Xiao, Wen-Jing
author_sort Liu, Jing
collection PubMed
description N-Heterocyclic carbenes (NHCs) are efficient Lewis basic catalysts for the umpolung of various polarized unsaturated compounds usually including aldehydes, imines, acyl chlorides and activated esters. NHC catalysis involving electron pair transfer steps has been extensively studied; however, NHC catalysis through single-electron transfer (SET) processes, despite having the potential to achieve chemical transformations of inert chemical bonds and using green reagents, has long been a challenging task in organic synthesis. In parallel, visible-light-induced photocatalysis and photoexcitation have been established as powerful tools to facilitate sustainable organic synthesis, as they enable the generation of various reactive radical intermediates under extremely mild conditions. Recently, a number of elegant visible-light-induced, NHC-catalyzed transformations were developed for accessing valuable organic compounds. As a result, this minireview will highlight the recent advances in this field.
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spelling pubmed-81623722021-06-04 Light opens a new window for N-heterocyclic carbene catalysis Liu, Jing Xing, Xiao-Ning Huang, Jin-Hai Lu, Liang-Qiu Xiao, Wen-Jing Chem Sci Chemistry N-Heterocyclic carbenes (NHCs) are efficient Lewis basic catalysts for the umpolung of various polarized unsaturated compounds usually including aldehydes, imines, acyl chlorides and activated esters. NHC catalysis involving electron pair transfer steps has been extensively studied; however, NHC catalysis through single-electron transfer (SET) processes, despite having the potential to achieve chemical transformations of inert chemical bonds and using green reagents, has long been a challenging task in organic synthesis. In parallel, visible-light-induced photocatalysis and photoexcitation have been established as powerful tools to facilitate sustainable organic synthesis, as they enable the generation of various reactive radical intermediates under extremely mild conditions. Recently, a number of elegant visible-light-induced, NHC-catalyzed transformations were developed for accessing valuable organic compounds. As a result, this minireview will highlight the recent advances in this field. The Royal Society of Chemistry 2020-08-11 /pmc/articles/PMC8162372/ /pubmed/34094315 http://dx.doi.org/10.1039/d0sc03595e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Liu, Jing
Xing, Xiao-Ning
Huang, Jin-Hai
Lu, Liang-Qiu
Xiao, Wen-Jing
Light opens a new window for N-heterocyclic carbene catalysis
title Light opens a new window for N-heterocyclic carbene catalysis
title_full Light opens a new window for N-heterocyclic carbene catalysis
title_fullStr Light opens a new window for N-heterocyclic carbene catalysis
title_full_unstemmed Light opens a new window for N-heterocyclic carbene catalysis
title_short Light opens a new window for N-heterocyclic carbene catalysis
title_sort light opens a new window for n-heterocyclic carbene catalysis
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162372/
https://www.ncbi.nlm.nih.gov/pubmed/34094315
http://dx.doi.org/10.1039/d0sc03595e
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