Acta Chimica Sinica ›› 1962, Vol. 28 ›› Issue (6): 398-400. Previous Articles    

16α-羥基16β-甲基孕甾烯化合物的合成

黄鳴龍, 陈毓羣   

  1. 中国科学院有机化学研究所
  • 投稿日期:1962-08-17 发布日期:2013-06-03

SYNTHESIS OF 16α-HYDROXY-16β-METHYLPREGNENES

HUANG-MINLON, CHEN YUH-CHENG   

  1. Institute of Organic Chemistry, Academia Sinica
  • Received:1962-08-17 Published:2013-06-03

Modified Kishner-Wolff reduction of 16α,17α-epoxy-l6β-methyl-Δ5-pregnene 3β-o1-20-one (Ⅱb) afforded a mirture of two 16β-methyl-Δ5.17(20)-pregnadien-3β,16α-diols Ⅳa+Ⅳb geometrically isomeric at C17-20. The structures of those compounds were proved by hydrogenation to compound Ⅴ, dehydration to compound Ⅵa, oxidation to compounds Ⅶa and Ⅶb and ozonization to yield acetaldehyde.