Synlett 2015; 26(20): 2784-2788
DOI: 10.1055/s-0035-1560531
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© Georg Thieme Verlag Stuttgart · New York

Nickel-Catalyzed Regioselective Reductive Cross-Coupling of Aryl Halides with Polysubstituted Allyl Halides in the Presence of Imidazolium Salts

Authors

  • Zhan Zhang

    Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou 310018, P. R. of China   Email: renhj@zstu.edu.cn
  • Lijun Xu

    Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou 310018, P. R. of China   Email: renhj@zstu.edu.cn
  • Zhengkai Chen

    Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou 310018, P. R. of China   Email: renhj@zstu.edu.cn
  • Zhubo Liu

    Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou 310018, P. R. of China   Email: renhj@zstu.edu.cn
  • Maozhong Miao

    Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou 310018, P. R. of China   Email: renhj@zstu.edu.cn
  • Jinyu Song

    Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou 310018, P. R. of China   Email: renhj@zstu.edu.cn
  • Hongjun Ren*

    Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou 310018, P. R. of China   Email: renhj@zstu.edu.cn
Further Information

Publication History

Received: 21 September 2015

Accepted after revision: 26 October 2015

Publication Date:
13 November 2015 (online)


Graphical Abstract

Abstract

The nickel-catalyzed direct reductive cross-coupling of aryl halides with readily accessible polysubstituted allyl halides provides an efficient method for preparing diverse allylated arenes under mild conditions. Both allyl bromides and allyl chlorides are compatible with the transformation.

Supporting Information