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Fluorinated oligosaccharides synthesis

Scheme 4. The two-stage activation method for oligosaccharide synthesis the use of thioglycosides as convenient sources of fluorinated glycosyl donors and application of the technology to the partial synthesis of avermectin (18). (Nicolaou, 1984) ... Scheme 4. The two-stage activation method for oligosaccharide synthesis the use of thioglycosides as convenient sources of fluorinated glycosyl donors and application of the technology to the partial synthesis of avermectin (18). (Nicolaou, 1984) ...
UDP-A-MurNAc-depsipentapeptide) derivatives including fluorescent-labeled derivatives. Shin-ichiro Nishimura et al. reported the synthesis of UDP-MurNAc-pentapeptide derivatives possessing a levulinyl (Lev) group on the side chain of the Lys residue [82, 83] for subsequent introduction of fluorescent label or oligosaccharide moieties by oxime formation after their incorporation through cell-wall biosynthesis. The 4-fluorinated UDP-MurNAc-pentapeptide was also synthesized as a stable biosynthesis inhibitor [84],... [Pg.370]


See other pages where Fluorinated oligosaccharides synthesis is mentioned: [Pg.52]    [Pg.622]    [Pg.601]    [Pg.1267]    [Pg.226]    [Pg.588]    [Pg.39]    [Pg.104]    [Pg.517]    [Pg.97]    [Pg.50]    [Pg.55]    [Pg.337]    [Pg.469]    [Pg.30]    [Pg.39]    [Pg.63]    [Pg.98]    [Pg.220]    [Pg.436]    [Pg.191]    [Pg.221]    [Pg.300]   
See also in sourсe #XX -- [ Pg.39 , Pg.40 ]




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