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Stereoselective glycosylations using selectivity

A novel strategy for stereoselective glycosylations has been reported in which a chiral auxiliary at the 2-position of a glycosyl donor is used (Scheme 126).189 Upon formation of an oxonium ion, participation of the nucleophilic moiety of the auxiliary is (g) selective and depedent on the chirality. [Pg.494]

See other pages where Stereoselective glycosylations using selectivity is mentioned: [Pg.133]    [Pg.89]    [Pg.377]    [Pg.36]    [Pg.43]    [Pg.256]    [Pg.261]    [Pg.282]    [Pg.391]    [Pg.98]    [Pg.106]    [Pg.206]    [Pg.216]    [Pg.307]    [Pg.308]    [Pg.313]    [Pg.572]    [Pg.112]    [Pg.591]    [Pg.533]    [Pg.440]    [Pg.537]    [Pg.1214]    [Pg.1251]    [Pg.1650]    [Pg.93]    [Pg.578]    [Pg.533]    [Pg.134]    [Pg.110]    [Pg.260]    [Pg.99]    [Pg.253]    [Pg.126]    [Pg.503]    [Pg.503]    [Pg.120]    [Pg.224]    [Pg.1144]    [Pg.514]    [Pg.646]    [Pg.649]    [Pg.40]    [Pg.43]    [Pg.52]    [Pg.65]    [Pg.91]    [Pg.117]   
See also in sourсe #XX -- [ Pg.82 ]



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Glycosylation stereoselectivity

Glycosylations glycosylation Stereoselective

Selectivity stereoselectivity

Stereoselective glycosylation

Stereoselective glycosylations using

Stereoselective glycosylations using anomeric selectivities

Stereoselective glycosylations using glycosylation

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