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Application to glycoside and nucleoside synthesis

In the reaction with 6-bromo-2-naphthol, no simple glycosides were obtained, but a mixture of tetracyclic compounds in yields of 32 % and 44 %, respectively (zirconocene activator). The hafnium reagent gave the same products in a similar ratio (21% and 44% yield) [30], [Pg.288]

2 Application to glycosylphosphatidylinositol (CPI) anchor and inositol phosphoglycan (IPG) synthesis [Pg.289]

Use of orthogonal activation strategies in the synthesis of a disaccharide donor. [Pg.292]


See other pages where Application to glycoside and nucleoside synthesis is mentioned: [Pg.287]    [Pg.525]    [Pg.287]   


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Application to synthesis

Glycosides synthesis

Glycosides, and glycosidation

Nucleoside synthesis

Synthesis applications

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