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Effects of α- and β-Galactosylated C2-Ceramides on the Immune System

✍ Scribed by Sakai, Teruyuki; Ueno, Hitomi; Natori, Takenori; Uchimura, Akira; Motoki, Kazuhiro; Koezuka, Yasuhiko

Book ID
127062401
Publisher
American Chemical Society
Year
1998
Tongue
English
Weight
38 KB
Volume
41
Category
Article
ISSN
0022-2623

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Predominant a-linked products can be generated in glycosylation involving galactosyl trichloroacetimidate donors with 2-naphthylmethyl (NAP) as the non-participating group at C-2 position. The above-mentioned donor was successfully utilized for the synthesis of a-galactosyl ceramide.