Abstract
Selective NaBH4 and CeCl3·7H2O/NaBH4 mediated reduction of the carbonyl group at C-12 in 22,26-oxacholestane derivatives, prepared by regioselective acid-catalyzed opening of botogenin acetate and hecogenin acetate, provided the respective 12α-hydroxycholestanes in high yield. The structures of the products were established by NMR techniques.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Monatshefte für Chemie und verwandte Teile anderer Wissenschaften
Paper Title
Journal
Date
