An enantiospecific route to C,D ring synthons for steroid synthesis

Autor: Clase, J. Andrew, Money, Thomas
Zdroj: Canadian Journal of Chemistry; May 1992, Vol. 70 Issue: 5 p1537-1544, 8p
Abstrakt: A simple enantiospecific route to a hydrindenone intermediate for steroid synthesis has been accomplished. The introduction of a wide variety of side-chain units is made possible by stereoselective alkylation of a bicyclic ester 13derived from (+)-camphor 4.
Databáze: Supplemental Index