STEREOSELECTIVE FORMATION OF GLYCOCONJUGATED LACTAMIDES FROM CHIRAL 2-BROMOPROPANAMIDES

Authors
NEJAD FMK MARCHETTI P RONDANIN R BARILI PL CATELANI G
Citation
Fmk. Nejad et al., STEREOSELECTIVE FORMATION OF GLYCOCONJUGATED LACTAMIDES FROM CHIRAL 2-BROMOPROPANAMIDES, Gazzetta chimica italiana, 124(2), 1994, pp. 65-69
Citations number
17
Categorie Soggetti
Chemistry
Journal title
Gazzetta chimica italiana → ACNP
ISSN journal
00165603
Volume
124
Issue
2
Year of publication
1994
Pages
65 - 69
Database
ISI
SICI code
0016-5603(1994)124:2<65:SFOGLF>2.0.ZU;2-8
Abstract
The silver oxide promoted reaction of chiral 2-bromopropanamides with 1,2:3,4-di-O-isopropylidene-D-galactopyranose or with 1,2:5,6-di-O-iso propylidene-D-glucofuranose takes place with complete stereoselectivit y and moderate chemical yield, giving diastereochemically pure glycoco njugate lactamides characterised through NMR spectroscopy.