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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...

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Autores principales: Talbot, Fabien J. T., Dherbassy, Quentin, Manna, Srimanta, Shi, Chunling, Zhang, Shibo, Howell, Gareth P., Perry, Gregory J. P., Procter, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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