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化学进展 2017, Vol. 29 Issue (1): 13-14 DOI: 10.7536/PC161238 前一篇   后一篇

所属专题: 中国化学印记

• 中国化学印记 •

铜催化的惰性苄位碳氢键的不对称氰基化反应

丁奎岭*   

  1. 中国科学院上海有机化学研究所 金属有机国家重点实验室 上海 200032
  • 出版日期:2017-01-05 发布日期:2017-01-10
  • 通讯作者: 丁奎岭 E-mail:kding@sioc.ac.cn

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

Kuiling Ding*   

  1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China
  • Online:2017-01-05 Published:2017-01-10
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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