Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1390836 | Carbohydrate Research | 2007 | 10 Pages |
Abstract
A mimic of a (1→2),(1→6)-mannotrioside was synthesized by replacing the central mannose unit with an enantiomerically pure, conformationally stable trans-diaxial cyclohexanediol. The three-dimensional structure of the molecule was investigated by NMR spectroscopy supported by molecular modelling and was compared to the known features of the natural mannotrioside.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Silvia Mari, Inmaculada Sánchez-Medina, Pierangelo Mereghetti, Laura Belvisi, Jesus Jiménez-Barbero, Anna Bernardi,