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Galactose trichloroacetimidate

Unprotected galactose derivatives may be readily transformed into the trichloroacetimidates 8a-8g, as shown in Table VIII. Again, as demonstrated for the O-benzyl-protected compounds 8a, either the a-trichloroace-timidate 8a-a or the / -trichloroacetimidate 8a -/ may be obtained highly selectively, depending on the base used for the catalysis of the addition to the trichloroacetonitrile. [Pg.53]

Glycosylation of Trichloroacetimidates of D-Galactose with Sphingosine Derivative 6B... [Pg.59]

Trichloroacetimidates may alo be used for the synthesis of 2-amino-2-deoxy-a-D-glycopyranosides particularly in the galactose series.36... [Pg.79]

Novel branched yS-CyDs with jS-o-galactose residues were chemically synthesized using the trichloroacetimidate method. Tetraacetyl galactosyl trichloroacetimidate was obtained with trichloacetonitrile in the presence of l,8-diazabicyclo[5.4.0] undec-7-ene (DBU) [101]. [Pg.39]


See other pages where Galactose trichloroacetimidate is mentioned: [Pg.407]    [Pg.407]    [Pg.407]    [Pg.407]    [Pg.49]    [Pg.52]    [Pg.58]    [Pg.84]    [Pg.98]    [Pg.98]    [Pg.96]    [Pg.176]    [Pg.297]    [Pg.292]    [Pg.312]    [Pg.292]    [Pg.124]    [Pg.385]    [Pg.48]    [Pg.103]    [Pg.205]    [Pg.775]    [Pg.785]    [Pg.785]    [Pg.1221]    [Pg.1251]    [Pg.415]    [Pg.157]    [Pg.175]    [Pg.305]    [Pg.318]    [Pg.487]    [Pg.83]    [Pg.187]    [Pg.765]    [Pg.775]    [Pg.775]    [Pg.250]    [Pg.36]    [Pg.15]    [Pg.31]    [Pg.65]    [Pg.24]    [Pg.69]    [Pg.129]   
See also in sourсe #XX -- [ Pg.315 ]




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Trichloroacetimidate

Trichloroacetimidates

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