532983-42-9Relevant articles and documents
An improved synthesis of methyl protodioscin: Tautomerization and direct access to the 3-o-substituted kryptogenin
Xu, Qing-Chun,Liu, Yang,Liu, Jiao,He, Chun-Xian,Yan, Mao-Cai,Cheng, Mao-Sheng
, p. 780 - 781 (2008/12/21)
The acid-catalyzed tautomerization of 3-O-substituted kryptogenin 2 was studied, and the effects of acids such as silica gel, TMSOTf, acetic acid, and CDCl3, are discussed. Additionally, a Zn/KI/HOAc reduction based on this tautomerization was adopted, which afforded 2 directly, and provided a facile procedure for the synthesis of methyl protodioscin and other furostanol saponins in a mild way. Copyright