ENANTIOSEPARATION OF N-(1-ARYLETHYL)AMIDES AND ALPHA-[N-(3,5-DINITROBENZOYL)]AMINO ESTERS BY COLUMN CHROMATOGRAPBY - CHIRAL RECOGNITION USING A HYDROGEN-BOND ACCEPTOR CENTERED IN A PSEUDO-C-2 SYMMETRICAL ENVIRONMENT .2.

Authors
KISHIKAWA K TAKADA Y KAWASHIMA K KOHMOTO S YAMAMOTO M YAMADA K
Citation
K. Kishikawa et al., ENANTIOSEPARATION OF N-(1-ARYLETHYL)AMIDES AND ALPHA-[N-(3,5-DINITROBENZOYL)]AMINO ESTERS BY COLUMN CHROMATOGRAPBY - CHIRAL RECOGNITION USING A HYDROGEN-BOND ACCEPTOR CENTERED IN A PSEUDO-C-2 SYMMETRICAL ENVIRONMENT .2., Tetrahedron : asymmetry, 7(6), 1996, pp. 1733-1739
Citations number
8
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
7
Issue
6
Year of publication
1996
Pages
1733 - 1739
Database
ISI
SICI code
0957-4166(1996)7:6<1733:EONAA>2.0.ZU;2-W
Abstract
Enantioseparation of N-(1-arylethyl)amides and alpha-[N-(3,5-dinitrobe nzoyl)]amino esters was achieved by column chromatography on silica ge l modified with a chiral acylurea which has two (S)-1-(1-naphthyl)ethy l moieties in a pseudo-C-2 symmetric position around an axis of the ur ea-carbonyl. Copyright (C) 1996 Elsevier Science Ltd