Chinese Journal of Organic Chemistry ›› 2021, Vol. 41 ›› Issue (7): 2707-2714.DOI: 10.6023/cjoc202103029 Previous Articles     Next Articles



王凯凯a, 陈绍维b, 李亚军b, 李达谅a,*(), 鲍红丽b,*()   

  1. a 福建师范大学南方生物医学研究中心&化学与材料学院 福州 350007
    b 中国科学院福建物质结构研究所 煤制乙二醇重点实验室 福州 350002
  • 收稿日期:2021-03-18 修回日期:2021-04-15 发布日期:2021-04-29
  • 通讯作者: 李达谅, 鲍红丽
  • 基金资助:
    国家自然科学基金(21871258); 国家自然科学基金(21922112); 国家自然科学基金(22001251); 福建师范大学校创新团队(IRTL1703)

Iron-Catalyzed Decarboxylative Heck-Type Alkylation of Conjugate 1,3-Dienes

Kaikai Wanga, Shaowei Chenb, Yajun Lib, Daliang Lia(), Hongli Baob()   

  1. a Biomedical Research Center of South China & College of Chemistry and Materials Science, Fujian Normal University, Fuzhou 350007
    b Key Laboratory of Coal to Ethylene Glycol and Its Related Technology, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002
  • Received:2021-03-18 Revised:2021-04-15 Published:2021-04-29
  • Contact: Daliang Li, Hongli Bao
  • Supported by:
    National Natural Science Foundation of China(21871258); National Natural Science Foundation of China(21922112); National Natural Science Foundation of China(22001251); Innovative Research Teams Program of Fujian Normal University(IRTL1703)

An iron-catalyzed decarboxylative Heck-type alkylation of conjugate 1,3-dienes with alkyl diacyl peroxides andt-butyl peresters is reported. This method offers an efficient approach to alkylation of 1,3-dienes with good yields, and in some cases with high selectivities. Late-stage alkylation of bioactive compounds was also found to be effective.

Key words: iron catalysis, 1,3-dienes, Heck-type alkylation, decarboxylation, peresters, diacyl peroxides