Consecutive alkene cross-metathesis/oxonium ylide formation-rearrangement: synthesis of the anti-HIV agent hyperolactone C.

Alpha-diazo-beta-ketoesters bearing allylic ether functionality undergo highly stereoselective Ru-carbene-catalyzed alkene cross-metathesis followed by Rh(2)(OAc)(4)-catalyzed oxonium ylide formation/[2,3] sigmatropic rearrangement in a one-flask operation and in a highly diastereoselective manner....

תיאור מלא

מידע ביבליוגרפי
Main Authors: Hodgson, D, Angrish, D, Erickson, S, Kloesges, J, Lee, C
פורמט: Journal article
שפה:English
יצא לאור: 2008