Back to Search
Start Over
Copper‐Catalyzed Borylative Couplings with C−N Electrophiles.
- 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]
- Subjects :
- *CYANO group
*ELECTROPHILES
*PHARMACEUTICAL chemistry
*DIOLEFINS
*CATALYSTS
*ALKENES
Subjects
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