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L,2-anhydro-3,4,6-tri-0-benzyl

H. Yamaguchi and C. Schuerch, Synthesis of l,2-anhydro-3,4,6-tri-0-benzyl-u-D-gluco-pyranose, Carbohydr. Res., 81 (1980) 192-195. [Pg.168]

Conformational analyses by n.m.r. and computational methods have been reported for the following compounds l,2-anhydro-3,4,6-tri-0-benzyl-P-D-talopyranose, anhydro sugars 13 and similar hexopyranose derivatives, methyl 3,4-0-isopropylidene-a- and P-D-galactopyranoside and their di-O-acetates and di-O-methyl ethers, 3,4-0-(/ )-benzylidene-D-ribono-1,5-lactone (see Chapter 6), and 6-deoxy-6-phosphonoyl-D-fructopyranoses (see Chapter 17 for synthesis). D-Glucospyranosylamine, its tetra-O-acetate and 4,6-0-benzylidene acetal and several N-acylated derivatives, together with D-[l- C]glucopyranosylamine, have been used in a conformational study by n.m.r. spectroscopy aimed at probing the existence of the reverse anomeric effect. ... [Pg.280]

See other pages where L,2-anhydro-3,4,6-tri-0-benzyl is mentioned: [Pg.171]    [Pg.208]    [Pg.169]    [Pg.169]    [Pg.132]    [Pg.251]    [Pg.92]    [Pg.42]    [Pg.166]    [Pg.118]    [Pg.368]    [Pg.41]    [Pg.106]    [Pg.109]    [Pg.149]    [Pg.36]    [Pg.118]    [Pg.118]    [Pg.19]    [Pg.239]   


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