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Photoinduced inverse Sonogashira coupling reaction
Alkynes are widely used in chemistry, medicine and materials science. Here we demonstrate a transition-metal and photocatalyst-free inverse Sonogashira coupling reaction between iodoalkynes and (hetero)arenes or alkenes under visible-light irradiation. Mechanistic and computational studies suggest t...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241966/ https://www.ncbi.nlm.nih.gov/pubmed/35872819 http://dx.doi.org/10.1039/d2sc01933g |
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author | Zhang, Lizhu Wei, Cunbo Wu, Jiawen Liu, Dan Yao, Yinchao Chen, Zhuo Liu, Jianxun Yao, Chang-Jiang Li, Dinghua Yang, Rongjie Xia, Zhonghua |
author_facet | Zhang, Lizhu Wei, Cunbo Wu, Jiawen Liu, Dan Yao, Yinchao Chen, Zhuo Liu, Jianxun Yao, Chang-Jiang Li, Dinghua Yang, Rongjie Xia, Zhonghua |
author_sort | Zhang, Lizhu |
collection | PubMed |
description | Alkynes are widely used in chemistry, medicine and materials science. Here we demonstrate a transition-metal and photocatalyst-free inverse Sonogashira coupling reaction between iodoalkynes and (hetero)arenes or alkenes under visible-light irradiation. Mechanistic and computational studies suggest that iodoalkynes can be directly activated by visible light irradiation, and an excited state iodoalkyne acted as an “alkynyl radical synthetic equivalent”, reacting with a series of C(sp(2))–H bonds for coupling products. This work should open new windows in radical chemistry and alkynylation method. |
format | Online Article Text |
id | pubmed-9241966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-92419662022-07-22 Photoinduced inverse Sonogashira coupling reaction Zhang, Lizhu Wei, Cunbo Wu, Jiawen Liu, Dan Yao, Yinchao Chen, Zhuo Liu, Jianxun Yao, Chang-Jiang Li, Dinghua Yang, Rongjie Xia, Zhonghua Chem Sci Chemistry Alkynes are widely used in chemistry, medicine and materials science. Here we demonstrate a transition-metal and photocatalyst-free inverse Sonogashira coupling reaction between iodoalkynes and (hetero)arenes or alkenes under visible-light irradiation. Mechanistic and computational studies suggest that iodoalkynes can be directly activated by visible light irradiation, and an excited state iodoalkyne acted as an “alkynyl radical synthetic equivalent”, reacting with a series of C(sp(2))–H bonds for coupling products. This work should open new windows in radical chemistry and alkynylation method. The Royal Society of Chemistry 2022-05-30 /pmc/articles/PMC9241966/ /pubmed/35872819 http://dx.doi.org/10.1039/d2sc01933g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Zhang, Lizhu Wei, Cunbo Wu, Jiawen Liu, Dan Yao, Yinchao Chen, Zhuo Liu, Jianxun Yao, Chang-Jiang Li, Dinghua Yang, Rongjie Xia, Zhonghua Photoinduced inverse Sonogashira coupling reaction |
title | Photoinduced inverse Sonogashira coupling reaction |
title_full | Photoinduced inverse Sonogashira coupling reaction |
title_fullStr | Photoinduced inverse Sonogashira coupling reaction |
title_full_unstemmed | Photoinduced inverse Sonogashira coupling reaction |
title_short | Photoinduced inverse Sonogashira coupling reaction |
title_sort | photoinduced inverse sonogashira coupling reaction |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241966/ https://www.ncbi.nlm.nih.gov/pubmed/35872819 http://dx.doi.org/10.1039/d2sc01933g |
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