34914-75-5Relevant articles and documents
Diastereoselective Aldol Reactions of Enolates Generated from Vicinally Substituted Trimethylsilylmethyl Cyclopropyl Ketones
Yadav, Veejendra K.,Balamurugan, Rengarajan
, p. 4281 - 4284 (2007/10/03)
(Equation presented) Vicinally substituted trimethylsilylmethyl cyclopropyl ketones undergo facile desilylative ring opening with Lewis acids under mild conditions. The enolates, thus generated, undergo aldol addition with aldehydes and ketones. The diast