Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1388619 | Carbohydrate Research | 2010 | 5 Pages |
Abstract
(2â²,3â²-O-Isopropylidene-5â²-uridyl) 4-(2,3,4,6-tetra-O-acetyl-β-d-glycopyranosyl)allophanates were obtained in the reactions of 2â²,3â²-O-isopropylidene-uridine and O-peracetylated β-d-gluco-, galacto- and xylopyranosylamines, and OCNCOCl. 2,3,4,6-Tetra-O-acetyl-β-d-glucopyranosyl isocyanate and N-(2â²,3â²-O-isopropylidene-5â²-uridyl)urea gave 1-(2,3,4,6-tetra-O-acetyl-β-d-glucopyranosyl)-5-(2â²,3â²-O-isopropylidene-5â²-uridyl)biuret. Deprotection of the β-d-gluco configured allophanate and biuret was carried out by standard methods.
Related Topics
Physical Sciences and Engineering
Chemistry
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Authors
Marietta Tóth, László Somsák,