Eintopfsynthese einer Trisaccharideinheit des gemeinen Polysaccharid‐Antigens von Streptococci der Gruppe B unter Verwendung Cyclohexan‐1,2‐diacetal(CDA)‐geschützter Rhamnoside
- 21 November 1994
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 106 (22) , 2412-2414
- https://doi.org/10.1002/ange.19941062227
Abstract
Die Reaktivität von Zuckern in Glycosylierungen kann die Cyclohexan‐1,2‐diacetal(CDA)‐Schutzgruppe wirksam regulieren. Aus drei Monosaccharidbausteinen läßt sich das Trisaccharid 1 synthetisieren, wobei zwischen den Glycosylierungsschritten keine Umwandlung funktioneller Gruppen notwendig ist. magnified imageKeywords
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