摘要

The highly stereoselective olefination reaction of alpha-fluoro-beta-keto esters for the synthesis of alpha-fluoro-alpha,beta-unsaturated esters has been developed. The olefination combines nucleophilic addition, intramolecular nucleophilic addition, and elimination in one step, as well as provides a facile synthetic approach to alpha-fluoro-alpha,beta-unsaturated esters which are important units in many biologically active compounds and useful precursors in a variety of functional-group transformations.