Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1388947 | Carbohydrate Research | 2009 | 5 Pages |
Abstract
A simple stereoselective synthesis of per-O-benzoyl-β-d-mannopyranosyl azide from per-O-benzoyl-α-d-mannopyranosyl bromide using phase transfer catalysis was developed. The stereochemistry at C-1 of the anomeric O-benzoylated α- and β-d-mannopyranosyl azides was unambiguously established using 2D NOESY NMR spectroscopy. Pure deprotected β-d-mannopyranosyl azide was prepared by debenzoylation with sodium methoxide in methanol.
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Authors
Polina I. Abronina, Vadim V. Kachala, Leonid O. Kononov,