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Copper‐Catalyzed Borylative Couplings with C−N Electrophiles.

Authors :
Talbot, Fabien J. T.
Dherbassy, Quentin
Manna, Srimanta
Shi, Chunling
Zhang, Shibo
Howell, Gareth P.
Perry, Gregory J. P.
Procter, David J.
Source :
Angewandte Chemie International Edition. 11/9/2020, Vol. 59 Issue 46, p20278-20289. 12p.
Publication Year :
2020

Abstract

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14337851
Volume :
59
Issue :
46
Database :
Academic Search Index
Journal :
Angewandte Chemie International Edition
Publication Type :
Academic Journal
Accession number :
146785867
Full Text :
https://doi.org/10.1002/anie.202007251