Boron enolates derived from alpha-heterosubstituted thioacetates and bearing menthone-derived chiral ligands react with aldehydes to give anti aldols with excellent diastero- and enantiocontrol.
A HIGHLY ENANTIOSELECTIVE AND DIASTEREOSELECTIVE ALDOL REACTION FOR ALPHA-HETEROSUBSTITUTED THIOACETATES / C.M.A. GENNARI, A. VULPETTI, D. MORESCA. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 35:27(1994), pp. 4857-4860.
A HIGHLY ENANTIOSELECTIVE AND DIASTEREOSELECTIVE ALDOL REACTION FOR ALPHA-HETEROSUBSTITUTED THIOACETATES
C.M.A. GENNARIPrimo
;
1994
Abstract
Boron enolates derived from alpha-heterosubstituted thioacetates and bearing menthone-derived chiral ligands react with aldehydes to give anti aldols with excellent diastero- and enantiocontrol.
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