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Glucosamine building block derivatives

O-allyl glucosamine building block 68. Finally, the controlled hydrogenolysis concept was applied to the synthesis of lactose derivatives (Scheme 4.17). [Pg.88]

Add (pick) saccharide residues from the list of aldoses (hexoses in al-dopyranose form, pentoses in aldofuranose form, and tetraoses in open-chain form), ketoses (hexoses in ketofuranose form, pentoses and tetraose in open-chain form), derivatives (glucosamine, galactosamine, N-acetylnuraminic acid, N-acetyl muramic acid, inositol, 2-deoxyribose, rhamnose, fucose, and apiose), and blocking groups (H, NH2, =0, COO—, methyl, lactyl, O-methyl, iV-methyl, O-acetyl, iV-acetyl, phosphoric acid, sulfate, iV-sulfonic acid) to build polysaccharides. [Pg.310]


See other pages where Glucosamine building block derivatives is mentioned: [Pg.258]    [Pg.354]    [Pg.257]    [Pg.84]    [Pg.272]    [Pg.340]    [Pg.32]    [Pg.257]    [Pg.781]    [Pg.496]    [Pg.510]    [Pg.153]    [Pg.39]    [Pg.487]    [Pg.771]    [Pg.51]    [Pg.251]    [Pg.53]    [Pg.658]    [Pg.53]    [Pg.271]    [Pg.1168]    [Pg.193]    [Pg.232]    [Pg.47]    [Pg.295]    [Pg.569]    [Pg.64]    [Pg.220]   
See also in sourсe #XX -- [ Pg.258 , Pg.259 ]




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