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Glycopyranosyl cation

Noyori and coworkers found that tetrafluorosilane or trimethylsilyl tri-flate catalyzes the condensation of appropriately protected glycopyranosyl fluorides with trimethylsilyl ethers or alcohols. The strong affinity of silicon for fluorine was considered to be the driving force for this reaction. In the case of Sip4, attack of a nucleophile on the glycosyl cation-SiFj ion-pair intermediate was anticipated. Thus, condensation of 2,3,4,6-tetra-O-benzyl-a- and - -D-glucopyranosyl fluorides (47a and 47fi) with methyl... [Pg.107]


See other pages where Glycopyranosyl cation is mentioned: [Pg.144]    [Pg.47]    [Pg.272]    [Pg.396]    [Pg.396]    [Pg.69]    [Pg.144]    [Pg.47]    [Pg.272]    [Pg.396]    [Pg.396]    [Pg.69]    [Pg.90]    [Pg.104]    [Pg.412]    [Pg.119]    [Pg.210]   
See also in sourсe #XX -- [ Pg.69 ]




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Glycopyranosylations

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