Synthesis 2014; 46(20): 2751-2756
DOI: 10.1055/s-0033-1338661
paper
© Georg Thieme Verlag Stuttgart · New York

Asymmetric Transfer Hydrogenation of 3-(Trifluoromethyl)quinolines

Authors

  • Ran-Ning Guo

    a   Department of Chemistry, Dalian University of Technology, Dalian 116012, P. R. of China
    b   State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, P. R. of China   Fax: +86(411)84379220   Email: ygzhou@dicp.ac.cn
  • Zhang-Pei Chen

    b   State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, P. R. of China   Fax: +86(411)84379220   Email: ygzhou@dicp.ac.cn
  • Xian-Feng Cai

    b   State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, P. R. of China   Fax: +86(411)84379220   Email: ygzhou@dicp.ac.cn
  • Yong-Gui Zhou*

    b   State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, P. R. of China   Fax: +86(411)84379220   Email: ygzhou@dicp.ac.cn
Further Information

Publication History

Received: 26 May 2014

Accepted after revision: 25 June 2014

Publication Date:
24 July 2014 (online)


Graphical Abstract

Abstract

A chiral phosphoric acid-catalyzed asymmetric transfer hydrogenation of 3-(trifluoromethyl)quinolines was successfully developed with up to 98% ee. The new method provides a direct and facile access to chiral 2,3-disubstituted 1,2,3,4-tetrahydroquinoline derivatives containing a stereogenic trifluoromethyl group.

Supporting Information