Palladium-Catalyzed Asymmetric Hydrofunctionalizations of Conjugated Dienes

  • Yuchao Wang ,
  • Jinbiao Liu ,
  • Zhitao He
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  • a Faculty of Materials Metallurgy and Chemistry, Jiangxi University of Science and Technology, Ganzhou, Jiiangxi 341000
    b CAS Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Shanghai 200032
    c University of Chinese Academy of Sciences, Beijing 100049

Received date: 2023-02-11

  Revised date: 2023-03-18

  Online published: 2023-04-10

Supported by

The National Natural Science Foundation of China(22071262); The Science and Technology Commission of Shanghai Municipality(22ZR1475200); The Shanghai Rising-Star Program(20QA1411300)

Abstract

Because of the broad substrate availability, high atom economy and efficient stereocontrol, palladium-catalzyed asymmetric hydrofunctionalizations of conjugated dienes have emerged as an efficient route to construct enantioenriched allylic motifs, including allylic C—C, C—N, C—S, C—P, C—Si and C—O bonds. The development, advance and mechanistic features of this area in the past decades are summarized. Based on the types of allylic stereogenic centers constructed via this strategy, the review is divided into six parts, including asymmetric hydroalkylation, hydroamination, hydrophosphinylation, hydrosulfonylation, hydrosilylation and hydroalkoxylation.

Cite this article

Yuchao Wang , Jinbiao Liu , Zhitao He . Palladium-Catalyzed Asymmetric Hydrofunctionalizations of Conjugated Dienes[J]. Chinese Journal of Organic Chemistry, 2023 , 43(8) : 2614 -2627 . DOI: 10.6023/cjoc202302010

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