884496-07-5Relevant academic research and scientific papers
An N-aryl-substituted oxazolidinone-containing ketone-catalyzed asymmetric epoxidation with hydrogen peroxide as the primary oxidant
Burke, Christopher P.,Shu, Lianhe,Shi, Yian
, p. 6320 - 6323 (2008/02/09)
(Chemical Equation Presented) Asymmetric epoxidation of various olefins with an N-aryl-substituted oxazolidinone-containing ketone as catalyst and hydrogen peroxide as the primary oxidant has been investigated, and up to 96% ee was obtained.
Enantioselective synthesis of 2-aryl cyclopentanones by asymmetric epoxidation and epoxide rearrangement
Shen, Yu-Mei,Wang, Bin,Shi, Yian
, p. 1429 - 1432 (2007/10/03)
(Chemical Equation Presented) Optically active epoxides are prepared by the highly enantioselective epoxidation of benzylidenecyclobutanes using a glucose-derived ketone as the catalyst and oxone as the oxidant. A subsequent Lewis acid catalyzed rearrange
