676324-07-5Relevant articles and documents
Mechanism and conditions for highly enantioselective epoxidation of α,β-enones using charge-accelerated catalysis by a rigid quaternary ammonium salt
Corey,Zhang, Fu-Yao
, p. 1287 - 1290 (1999)
(Matrix presented) Highly enantioselective (up to 130:1) epoxidation of a variety of α,β-enones to form α,β-epoxy ketones is described along with a rational analysis of the mechanistic basis for this strong absolute stereochemical control by the chiral ca
Optically active epoxy compounds and processes for their production
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Page 14, (2010/11/30)
An optically active epoxyenone derivative of the following formula (1): wherein R1 is a methyl group, an ethyl group or a C3-10 branched, linear or cyclic alkyl group, and R2 is a phenyl group, a substituted phenyl group o