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Copper-catalyzed functionalization of enynes
The copper-catalyzed functionalization of enyne derivatives has recently emerged as a powerful approach in contemporary synthesis. Enynes are versatile and readily accessible substrates that can undergo a variety of reactions to yield densely functionalized, enantioenriched products. In this perspec...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163025/ https://www.ncbi.nlm.nih.gov/pubmed/34094380 http://dx.doi.org/10.1039/d0sc04012f |
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author | Dherbassy, Quentin Manna, Srimanta Talbot, Fabien J. T. Prasitwatcharakorn, Watcharapon Perry, Gregory J. P. Procter, David J. |
author_facet | Dherbassy, Quentin Manna, Srimanta Talbot, Fabien J. T. Prasitwatcharakorn, Watcharapon Perry, Gregory J. P. Procter, David J. |
author_sort | Dherbassy, Quentin |
collection | PubMed |
description | The copper-catalyzed functionalization of enyne derivatives has recently emerged as a powerful approach in contemporary synthesis. Enynes are versatile and readily accessible substrates that can undergo a variety of reactions to yield densely functionalized, enantioenriched products. In this perspective, we review copper-catalyzed transformations of enynes, such as boro- and hydrofunctionalizations, copper-mediated radical difunctionalizations, and cyclizations. Particular attention is given to the regiodivergent functionalization of 1,3-enynes, and the current mechanistic understanding of such processes. |
format | Online Article Text |
id | pubmed-8163025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81630252021-06-04 Copper-catalyzed functionalization of enynes Dherbassy, Quentin Manna, Srimanta Talbot, Fabien J. T. Prasitwatcharakorn, Watcharapon Perry, Gregory J. P. Procter, David J. Chem Sci Chemistry The copper-catalyzed functionalization of enyne derivatives has recently emerged as a powerful approach in contemporary synthesis. Enynes are versatile and readily accessible substrates that can undergo a variety of reactions to yield densely functionalized, enantioenriched products. In this perspective, we review copper-catalyzed transformations of enynes, such as boro- and hydrofunctionalizations, copper-mediated radical difunctionalizations, and cyclizations. Particular attention is given to the regiodivergent functionalization of 1,3-enynes, and the current mechanistic understanding of such processes. The Royal Society of Chemistry 2020-10-07 /pmc/articles/PMC8163025/ /pubmed/34094380 http://dx.doi.org/10.1039/d0sc04012f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Dherbassy, Quentin Manna, Srimanta Talbot, Fabien J. T. Prasitwatcharakorn, Watcharapon Perry, Gregory J. P. Procter, David J. Copper-catalyzed functionalization of enynes |
title | Copper-catalyzed functionalization of enynes |
title_full | Copper-catalyzed functionalization of enynes |
title_fullStr | Copper-catalyzed functionalization of enynes |
title_full_unstemmed | Copper-catalyzed functionalization of enynes |
title_short | Copper-catalyzed functionalization of enynes |
title_sort | copper-catalyzed functionalization of enynes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163025/ https://www.ncbi.nlm.nih.gov/pubmed/34094380 http://dx.doi.org/10.1039/d0sc04012f |
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