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铜催化的惰性苄位碳氢键的不对称氰基化反应

丁奎岭*

化学进展 ›› 2017, Vol. 29 ›› Issue (1) :13-14

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化学进展 ›› 2017, Vol. 29 ›› Issue (1) :13-14 DOI: 10.7536/PC161238
中国化学印记
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铜催化的惰性苄位碳氢键的不对称氰基化反应

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

  • Kuiling Ding*
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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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丁奎岭. 铜催化的惰性苄位碳氢键的不对称氰基化反应[J]. 化学进展, 2017, 29(1): 13-14 DOI:10.7536/PC161238
Kuiling Ding. Enantioselective Cyanation of Benzylic C-H Bonds via Copper-Catalyzed Radical Delay[J]. Progress in Chemistry, 2017, 29(1): 13-14 DOI:10.7536/PC161238

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参考文献

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