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Amylose sulfate structure

A. Richter and W. Wagenknecht, Synthesis of amylose acetates and amylose sulfates with high structural uniformity, Carbohydr. Res., 338 (2003) 1397-1401. [Pg.192]

Polysaccharides Hydrogen bonds and dipole-dipole interactions with hydroxyl groups of the sugar molecules are assumed to be the main interactions. In some cases, the helical structure of dextrins might be responsible for chiral recognition. Heparin, dextran sulfate, dermatan sulfate, streptomycin sulfate, amylose, chondroitin sulfate C, laminaran, dextrin sulfopropyl, and kanamycin sulfate. Doxylamine, laudanosine, naproxen, oxamniquine, pheniramine, primaquine, timepidium, trimetoquinol, etc. [Pg.453]

See other pages where Amylose sulfate structure is mentioned: [Pg.15]    [Pg.336]    [Pg.489]    [Pg.474]    [Pg.224]    [Pg.224]    [Pg.262]    [Pg.736]    [Pg.319]    [Pg.366]    [Pg.252]    [Pg.347]    [Pg.422]    [Pg.39]   
See also in sourсe #XX -- [ Pg.29 , Pg.336 ]

See also in sourсe #XX -- [ Pg.336 ]



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Sulfation structure

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