Enantioselective synthesis of the optically active alpha-methylene-beta-hydroxy esters, equivalent compounds to Morita-Baylis-Hillman adducts, using successive asymmetric aldol reaction and oxidative deselenization.

Shiina, Isamu

Enantioselective synthesis of the optically active alpha-methylene-beta-hydroxy esters, equivalent compounds to Morita-Baylis-Hillman adducts, using successive asymmetric aldol reaction and oxidative deselenization. [electronic resource] - The Journal of organic chemistry Sep 2005 - 8103-6 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0022-3263

10.1021/jo051276y doi


Esters
Hydroxy Acids--chemistry
Methylation
Methylene Chloride--chemistry
Models, Molecular
Molecular Conformation
Oxidation-Reduction
Stereoisomerism