Issue 40, 2015

Enantioselective 1,4-addition of cyclopropylboronic acid catalyzed by rhodium/chiral diene complexes

Abstract

Rhodium-catalyzed asymmetric addition of cyclopropylboronic acids to electron-deficient alkenes such as alkenylsulfones, enones, enoates, and nitroalkenes proceeded to give high yields of the corresponding 1,4-addition products with high enantioselectivity.

Graphical abstract: Enantioselective 1,4-addition of cyclopropylboronic acid catalyzed by rhodium/chiral diene complexes

Supplementary files

Article information

Article type
Communication
Submitted
13 Mar 2015
Accepted
09 Apr 2015
First published
10 Apr 2015
This article is Open Access
Creative Commons BY license

Chem. Commun., 2015,51, 8528-8531

Enantioselective 1,4-addition of cyclopropylboronic acid catalyzed by rhodium/chiral diene complexes

R. Takechi and T. Nishimura, Chem. Commun., 2015, 51, 8528 DOI: 10.1039/C5CC02140E

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