Armed-Disarmed Concept in the Synthesis of Glycosidic Bond

Armed-Disarmed Concept in the Synthesis of Glycosidic Bond 

Fraser-Reid et al. reported [1] that n-pentenyl glycosides undergo chetnospecific cleavage i — 2 3, with W-bromosuccinimide under conditions that leave a wide variety of other protecting groups unaffected (Fig. 5.1). 

Miljkovic, Electrostatic and Stereoelectronic Effects in Carbohydrate Chemistry, 

Veeneman and van Boom [6] have attempted to synthesize L-rhamnose-containing fragments from Streptococcus pneumoniae type-specific capsular 

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