ENANTIOSELECTIVE SYNTHESIS OF OPTICALLY-ACTIVE METOLACHLOR VIA ASYMMETRIC REDUCTION

Authors
CHO BT CHUN YS
Citation
Bt. Cho et Ys. Chun, ENANTIOSELECTIVE SYNTHESIS OF OPTICALLY-ACTIVE METOLACHLOR VIA ASYMMETRIC REDUCTION, Tetrahedron : asymmetry, 3(3), 1992, pp. 337-340
Citations number
10
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
3
Issue
3
Year of publication
1992
Pages
337 - 340
Database
ISI
SICI code
0957-4166(1992)3:3<337:ESOOMV>2.0.ZU;2-0
Abstract
Optically active metolachlor was prepared by chloroacetylation of the corresponding amine obtained by asymmetric reduction of the requisite imine with the chiral hydrides, such as Itsuno's reagent (4), Corey's reagent (5) and K glucoride (6).