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Title: An expeditious enantioselective total synthesis of valilactone. Author: Wu Y, Sun YP. Journal: J Org Chem; 2006 Jul 21; 71(15):5748-51. PubMed ID: 16839158. Abstract: The title compound was synthesized through an expeditious route using Crimmins aldolization to establish the two key stereogenic centers and a hydroxyl group activation (HGA) protocol to construct the anti alpha,beta-disubstituted beta-lactone from the corresponding syn aldol.[Abstract] [Full Text] [Related] [New Search]