546
3
Chemical Glycosylation Reactions
⊡ Scheme 46
(Ref. [54])
⊡ Scheme 47
(Ref. [56])
⊡ Scheme 48
(Ref. [59])
and coworkers applied Terashima’s method to their synthetic study on everninomicin antibiotics ( > Scheme 50) [61]. Rosso et al. reported the use of the 1-O-(p-nitrobenzoyl)glycosyl
donor for the practical synthesis of Disaccharide H, 2-O-(α-L-fucopyranosyl)-D-galactopyranose—which is one of the biologically important L-fucose-containing oligosaccharides—in
3
Chemical Glycosylation Reactions
⊡ Scheme 46
(Ref. [54])
⊡ Scheme 47
(Ref. [56])
⊡ Scheme 48
(Ref. [59])
and coworkers applied Terashima’s method to their synthetic study on everninomicin antibiotics ( > Scheme 50) [61]. Rosso et al. reported the use of the 1-O-(p-nitrobenzoyl)glycosyl
donor for the practical synthesis of Disaccharide H, 2-O-(α-L-fucopyranosyl)-D-galactopyranose—which is one of the biologically important L-fucose-containing oligosaccharides—in