Issue 9, 2014

Copper(i)-catalyzed enantioselective hydroboration of cyclopropenes: facile synthesis of optically active cyclopropylboronates

Abstract

Copper(I)-catalyzed enantioselective hydroboration of 3-aryl substituted cyclopropene-3-carboxylate is described, providing chiral cyclopropylboronates with excellent enantioselectivities (89–95% ee) in moderate to high yields (55–86%). The non-directing effect of the ester group was observed, and the reaction proceeded with solely trans-selectivity. The chiral boronates could be conveniently converted into chiral 1,2-diaryl substituted cyclopropane derivatives.

Graphical abstract: Copper(i)-catalyzed enantioselective hydroboration of cyclopropenes: facile synthesis of optically active cyclopropylboronates

Supplementary files

Article information

Article type
Research Article
Submitted
28 máj 2014
Accepted
05 sep 2014
First published
10 sep 2014

Org. Chem. Front., 2014,1, 1116-1122

Copper(I)-catalyzed enantioselective hydroboration of cyclopropenes: facile synthesis of optically active cyclopropylboronates

B. Tian, Q. Liu, X. Tong, P. Tian and G. Lin, Org. Chem. Front., 2014, 1, 1116 DOI: 10.1039/C4QO00157E

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