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Enantioselective Cyanation of Benzylic C-H Bonds via Copper-Catalyzed Radical Delay

Progress in Chemistry ›› 2017, Vol. 29 ›› Issue (1) : 13 -14.

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Progress in Chemistry ›› 2017, Vol. 29 ›› Issue (1) : 13-14 DOI: 10.7536/PC161238
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Enantioselective Cyanation of Benzylic C-H Bonds via Copper-Catalyzed Radical Delay
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Abstract

C-H bond functionalization refers to transformations that introduce functional group directly via the cleavage of C-H bond, which shows excellent step- and atom-economy. A recent breakthrough was achieved by the Guosheng Liu group in collaboration with Shannon S. Stahl group from University of Wisconsin-Madison. They discovered a new strategy to achieve Cu-catalyzed enantioselective cyanation of benzylic C-H bonds via a "Radical Relay Process". The present copper-catalyzed method provides a remarkably chemo-, regio- and enantioselectivity to afford optical organonitriles efficiently under mild reaction conditions.

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Kuiling Ding. Enantioselective Cyanation of Benzylic C-H Bonds via Copper-Catalyzed Radical Delay. Progress in Chemistry, 2017, 29(1): 13-14 DOI:10.7536/PC161238

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