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Pd-Catalyzed Isomerization of Alkenes

  • Hong-Chao Chen ,
  • Yichen Wu ,
  • Yang Yu ,
  • Peng Wang
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  • a College of Science, Shanghai University, Shanghai 201900
    b State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Shanghai 200032
    c CAS Key Laboratory of Energy Regulation Materials, Shanghai Institute of Organic Chemistry, Shanghai 200032
    d School of Chemistry and Material Sciences, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou 310024
* Corresponding author. E-mail:

Received date: 2021-09-28

  Revised date: 2021-11-03

  Online published: 2021-11-17

Supported by

National Natural Science Foundation of China(22171277); National Natural Science Foundation of China(22101291); National Natural Science Foundation of China(21821002); Shanghai Rising-Star Program(20QA1411400)

Abstract

Starting from commercially available simple olefins, alkene isomerization could realize the efficient construction of multi-substituted alkenes, which might be difficult to access with other synthetic methods, in an atom-economic manner via the stereoselective or positional-selective modulation of the carbon-carbon double bonds. The palladium catalyzed stereoselective (Z/E) and the positional selective isomerization reactions of alkenes are summarized. The mechanistic perspectives, and their synthetic applications in the synthesis of drug molecules and natural products are discussed in detail.

Cite this article

Hong-Chao Chen , Yichen Wu , Yang Yu , Peng Wang . Pd-Catalyzed Isomerization of Alkenes[J]. Chinese Journal of Organic Chemistry, 2022 , 42(3) : 742 -757 . DOI: 10.6023/cjoc202109045

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