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-isopropylidene-D-glucofuranose takes place with complete stereoselectivity and moderate chemical yield, giving diastereochemically pure glycoconjugate lactamides characterised through NMR spectroscopy.
STEREOSELECTIVE FORMATION OF GLYCOCONJUGATED LACTAMIDES FROM CHIRAL 2-BROMOPROPANAMIDES
CATELANI, GIORGIO;
1994-01-01
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-isopropylidene-D-glucofuranose takes place with complete stereoselectivity and moderate chemical yield, giving diastereochemically pure glycoconjugate lactamides characterised through NMR spectroscopy.File in questo prodotto:
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