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

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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.

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Tian, B., Liu, Q., Tong, X., Tian, P., & Lin, G. Q. (2014). Copper(I)-catalyzed enantioselective hydroboration of cyclopropenes: Facile synthesis of optically active cyclopropylboronates. Organic Chemistry Frontiers, 1(9), 1116–1122. https://doi.org/10.1039/c4qo00157e

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