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Copper‐Catalyzed Borylative Couplings with C−N Electrophiles
Copper‐catalyzed borylative multicomponent reactions (MCRs) involving olefins and C−N electrophiles are a powerful tool to rapidly build up molecular complexity. The products from these reactions contain multiple functionalities, such as amino, cyano and boronate groups, that are ubiquitous in medic...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689787/ https://www.ncbi.nlm.nih.gov/pubmed/32544295 http://dx.doi.org/10.1002/anie.202007251 |
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author | Talbot, Fabien J. T. Dherbassy, Quentin Manna, Srimanta Shi, Chunling Zhang, Shibo Howell, Gareth P. Perry, Gregory J. P. Procter, David J. |
author_facet | Talbot, Fabien J. T. Dherbassy, Quentin Manna, Srimanta Shi, Chunling Zhang, Shibo Howell, Gareth P. Perry, Gregory J. P. Procter, David J. |
author_sort | Talbot, Fabien J. T. |
collection | PubMed |
description | Copper‐catalyzed borylative multicomponent reactions (MCRs) involving olefins and C−N electrophiles are a powerful tool to rapidly build up molecular complexity. The products from these reactions contain multiple functionalities, such as amino, cyano and boronate groups, that are ubiquitous in medicinal and process chemistry programs. Copper‐catalyzed MCRs are particularly attractive because they use a relatively abundant and non‐toxic catalyst to selectively deliver high‐value products from simple feedstocks such as olefins. In this Minireview, we explore this rapidly emerging field and survey the borylative union of allenes, dienes, styrenes and other olefins, with imines, nitriles and related C−N electrophiles. |
format | Online Article Text |
id | pubmed-7689787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76897872020-12-08 Copper‐Catalyzed Borylative Couplings with C−N Electrophiles Talbot, Fabien J. T. Dherbassy, Quentin Manna, Srimanta Shi, Chunling Zhang, Shibo Howell, Gareth P. Perry, Gregory J. P. Procter, David J. Angew Chem Int Ed Engl Minireviews Copper‐catalyzed borylative multicomponent reactions (MCRs) involving olefins and C−N electrophiles are a powerful tool to rapidly build up molecular complexity. The products from these reactions contain multiple functionalities, such as amino, cyano and boronate groups, that are ubiquitous in medicinal and process chemistry programs. Copper‐catalyzed MCRs are particularly attractive because they use a relatively abundant and non‐toxic catalyst to selectively deliver high‐value products from simple feedstocks such as olefins. In this Minireview, we explore this rapidly emerging field and survey the borylative union of allenes, dienes, styrenes and other olefins, with imines, nitriles and related C−N electrophiles. John Wiley and Sons Inc. 2020-07-28 2020-11-09 /pmc/articles/PMC7689787/ /pubmed/32544295 http://dx.doi.org/10.1002/anie.202007251 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Minireviews Talbot, Fabien J. T. Dherbassy, Quentin Manna, Srimanta Shi, Chunling Zhang, Shibo Howell, Gareth P. Perry, Gregory J. P. Procter, David J. Copper‐Catalyzed Borylative Couplings with C−N Electrophiles |
title | Copper‐Catalyzed Borylative Couplings with C−N Electrophiles |
title_full | Copper‐Catalyzed Borylative Couplings with C−N Electrophiles |
title_fullStr | Copper‐Catalyzed Borylative Couplings with C−N Electrophiles |
title_full_unstemmed | Copper‐Catalyzed Borylative Couplings with C−N Electrophiles |
title_short | Copper‐Catalyzed Borylative Couplings with C−N Electrophiles |
title_sort | copper‐catalyzed borylative couplings with c−n electrophiles |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689787/ https://www.ncbi.nlm.nih.gov/pubmed/32544295 http://dx.doi.org/10.1002/anie.202007251 |
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