A convenient procedure for the synthesis of 3β-hydroxy-6-oxo-5α-steroids.: Application to the synthesis of laxogenin

被引:15
|
作者
Iglesias-Arteaga, MA
Símuta-Lopez, EM
Xochihua-Moreno, S
Viñas-Bravo, O
Smith, SM
Reyes, SM
Sandoval-Ramírez, JS
机构
[1] Univ Nacl Autonoma Mexico, Fac Quim, Dept Quim Organ, Mexico City 04510, DF, Mexico
[2] Benemer Univ Autonoma Puebla, Fac Ciencias Quim, Puebla 72570, Mexico
关键词
laxogenin; diastereoselective epoxidation; 3; beta-hydroxy-6-oxo-5; alpha-steroids;
D O I
10.1590/S0103-50532005000300011
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A convenient pathway to obtain 3 beta-hydroxy-6-oxo-5 alpha-steroids from 3 beta-acetoxy Delta(5)-steroids is reported; the methodology was applied to the synthesis of laxogenin (7), substance that behaves as a plant growth hormone. This is an alternative way to produce an important functionality found in many examples of naturally occurring steroids. The developed procedure uses inexpensive reagents and can be carried out in four steps. The oxidizing and acidic steps used in this methodology did not affect the labile spiroketal side chain present in diosgenin (16).
引用
收藏
页码:381 / 385
页数:5
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