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  • 标题:Studies on Anthelmintics. XXXI. The Configuration of Stereoisomers of Ethyl 11-Ethoxycarbonyl-6α-hydroxy-3-oxoeusanton-4-enic Acid Lactone
  • 本地全文:下载
  • 作者:Masao Sumi
  • 期刊名称:Chemical and Pharmaceutical Bulletin
  • 印刷版ISSN:0009-2363
  • 电子版ISSN:1347-5223
  • 出版年度:1956
  • 卷号:4
  • 期号:3
  • 页码:152-157
  • DOI:10.1248/cpb1953.4.152
  • 出版社:The Pharmaceutical Society of Japan
  • 摘要:Configurational assignment has been made for three isomeric compounds obtained by the performic acid-oxidation of the enol acetate (II). The major product, which became an important intermediate for the total synthesis of santonin, has been given the structure of ethyl 11-ethoxycarbonyl-6α-hydroxy-3-oxo-11-epi-eusanton-4-enic acid lactone (III), and the other two were proved to be the C11-and the C6-epimer of (III). The mechanism of the oxidation reaction is also discussed briefly.
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