NATURAL PRODUCT RESEARCH AND DEVELOPMENT ›› 2017, Vol. 29 ›› Issue (9): 1475-1478. doi: 10.16333/j.1001-6880.2017.9.004

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Synthesis of Key Intermediate of Malyngamide K via Baylis-Hillman Reaction

DUAN Shu-hui1, SHI Qun1, ZHANG Jun-tao2*   

  1. 1School of Health Sciences, Wuhan University, Wuhan 430072, China; 2School of Chemical and Environmental Engineering, Wuhan Polytechnic University, Wuhan 430023,China
  • Online:2017-09-27 Published:2017-09-27

Abstract: Malyngamide K is a typical example of malyngamides with both cyclohexenone and allyl chloride moieties.The construction of its amine carbon skeleton is very important for the design of general synthetic route of those malyngamides.In this work,the amine carbon skeleton of malyngamide K was constructed between ethanol amine (2) and cyclohexanone (5) by BaylisHillman reaction,which provides a new synthetic route for those malyngamide analogues with both cyclohexenone and allyl chloride substructures.

Key words: organic chemistry, Baylis-Hillman reaction, synthesis, malyngamide K

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