25518-21-2Relevant academic research and scientific papers
An efficient asymmetric synthesis of substituted phenyl glycidic esters
Baures,Eggleston,Flisak,Gombatz,Lantos,Mendelson,Remich
, p. 6501 - 6504 (2007/10/02)
Chiral substituted glycidic esters have been prepared from their corresponding chalcones via a two step procedure consisting of an asymmetric epoxidation mediated by a poly-L-leucine polymer, followed by a previously unreported Baeyer-Villiger oxidation. The regioselectivity of this latter procedure was found to depend on the aryl substituent.
