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Glycosylation Reactions with Conformationally Armed Glycosyl Donors

2 Glycosylation Reactions with Conformationally Armed Glycosyl Donors [Pg.131]

5 Armed-Disanned Concept in the Synthesis of Glycosidic Bond [Pg.132]

The implications of these findings are quite far-reaching. The large boost in reactivity found caused by ring inversion of some saccharides suggests that [Pg.132]

These findings, furthermore, offer a new explanation that does not rely on the questioned stereoelectronic effect as to why enzymes may change the conformation of a monosaccharide s unit or possibly preferentially stabilize the 6-OH in the gg orientation 87 (06-C6-C5-05) to make the substrate more reactive (Fig. 5.26). [Pg.133]


See other pages where Glycosylation Reactions with Conformationally Armed Glycosyl Donors is mentioned: [Pg.163]    [Pg.206]    [Pg.225]   


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Glycosylation conformation

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