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Stereoselective Synthesis of (±) Neocnidilide
引用本文:Xiao Zhen JIAO,Ping XIE*,Lian Suo ZU,Xiao Tian LIANG Institute of Materia Medica,Chinese Academy of Medical Sciences & Peking Union Medical College,Beijing 100050. Stereoselective Synthesis of (±) Neocnidilide[J]. 中国化学快报, 2003, 14(2)
作者姓名:Xiao Zhen JIAO  Ping XIE*  Lian Suo ZU  Xiao Tian LIANG Institute of Materia Medica  Chinese Academy of Medical Sciences & Peking Union Medical College  Beijing 100050
作者单位:Xiao Zhen JIAO,Ping XIE*,Lian Suo ZU,Xiao Tian LIANG Institute of Materia Medica,Chinese Academy of Medical Sciences & Peking Union Medical College,Beijing 100050
摘    要:The lactone neocnidilide 8 occur in the roots of Cnidilide officinale1 which is shown to inhibit the growth and toxin production of mycotoxin-producing fungi2. Although The synthesis of lactones 7, which is stereoisomer of cnidilide, and 8 had been reported by others3, 4, we would like to report the highly stereoselective synthesis of its racemic isomer 8 as shown in Scheme 1. Scheme 1 COOHHOOCbcOOHH1234d5eOHOHHH 6fOOHHH 7g8COOHOHa12345673a7aOHHOH1235673 a7a1234561'1'2'…


Stereoselective Synthesis of (±) Neocnidilide
Xiao Zhen JIAO,Ping Xie,Lian Suo ZU,Xiao Tian LIANG. Stereoselective Synthesis of (±) Neocnidilide[J]. Chinese Chemical Letters, 2003, 14(2)
Authors:Xiao Zhen JIAO  Ping Xie  Lian Suo ZU  Xiao Tian LIANG
Abstract:The racemic neocnidilide has been synthesized by stereoselective reaction of hemiacetal 5 with n-BuMgBr.
Keywords:Neocnidilide   stereoselective   synthesis.
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