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Glycosylations nucleophilic substitution, aglycone carbon

In a different approach to the preparation of glycosides, the nucleophilic substitution takes place at the carbon atom of the aglycone rather than at the anomeric carbon (Scheme 4.53). In contrast to the methods discussed in Section 4.3, there is no scission of the glycosyl-oxygen bond in these reactions. Instead, the R-X bond is cleaved. [Pg.163]


See other pages where Glycosylations nucleophilic substitution, aglycone carbon is mentioned: [Pg.163]    [Pg.144]    [Pg.242]    [Pg.277]    [Pg.60]   
See also in sourсe #XX -- [ Pg.144 , Pg.145 ]




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Aglycon

Aglycon glycosylation

Aglycone

Aglycones

Aglycons

Carbon nucleophile

Carbon nucleophiles

Carbon nucleophiles, substitution

Carbonates glycosylations, nucleophilic substitution

Glycosyl carbonates

Glycosyl nucleophilic substitutions

Glycosylations by Nucleophilic Substitution at the Aglycone Carbon

Nucleophilic substitution carbon

Nucleophilic substitutions glycosylations

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