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Sugar acetates, acid-catalyzed anomerization

This process is the main course for the acid-catalyzed anomerization of sugar acetates, methyl glycosides, and related compounds in non-aqueous solvents.104,244,245 260,263 In many instances, formation of the cyclic carbonium ion is assisted by participation of a neighboring acetyl group,104 but this process is not a necessary feature. Anomerization of tetra-O-acetyl-2-deoxy-a-D-arafomo-hexopyranose takes place through a cyclic carbonium ion as depicted.245[Pg.43]


See other pages where Sugar acetates, acid-catalyzed anomerization is mentioned: [Pg.146]    [Pg.44]    [Pg.131]    [Pg.285]    [Pg.480]    [Pg.738]    [Pg.1428]    [Pg.480]    [Pg.209]    [Pg.139]    [Pg.160]    [Pg.334]    [Pg.245]    [Pg.309]    [Pg.293]    [Pg.245]   
See also in sourсe #XX -- [ Pg.24 , Pg.43 ]




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Acetals, acid catalyzed

Acetates, anomeric

Acidic sugars

Anomeric sugars

Anomerization acid-catalyzed

Sugars acetals

Sugars acetates

Sugars, acetates, anomerization

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