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Azidosphingosine

Azidosphingosine 13 was received in different synthetic pathways.32 The synthesis by Schmidt33 is mentioned here. [Pg.261]

Peng George Wang and coworkers reported [69] the total synthesis of iGb3Cer by using the azidosphingosine glycosylation procedure (Scheme 12.7). The lactosyl 3 -OH acceptor 34 was prepared from lactose via anomeric benzylation, tin-mediated... [Pg.303]

The azidosphingosine (13) is connected with the oligosaccharide. The azide is transformed to an amino functionality. [Pg.260]

See other pages where Azidosphingosine is mentioned: [Pg.41]    [Pg.179]    [Pg.179]    [Pg.180]    [Pg.41]    [Pg.45]    [Pg.49]    [Pg.305]    [Pg.305]    [Pg.312]    [Pg.260]    [Pg.261]    [Pg.299]    [Pg.300]    [Pg.304]    [Pg.305]    [Pg.307]    [Pg.311]    [Pg.261]    [Pg.163]    [Pg.490]    [Pg.490]    [Pg.482]    [Pg.483]    [Pg.1638]    [Pg.1640]    [Pg.1640]    [Pg.53]    [Pg.53]    [Pg.163]    [Pg.490]    [Pg.490]    [Pg.490]    [Pg.467]    [Pg.53]    [Pg.53]   
See also in sourсe #XX -- [ Pg.260 ]

See also in sourсe #XX -- [ Pg.299 , Pg.300 , Pg.303 , Pg.305 , Pg.311 ]



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Azidosphingosine glycosylation procedure

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