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Hydrides trifluoride, structure

The value of methylation studies in structural determination of carbohydrates is well known. Methylation of sucrose has generally been achieved by the use of dimethyl sulfate-sodium hydroxide,34,35 methyl iodide-silver oxide-acetone,20 sodium hydride-methyl io-dide-N,N-dimethylformamide,35 or diazomethane-boron trifluoride etherate.36,37 The last method (already applied to monosaccharides38,39) has been found particularly useful for sucrose, because it proceeds without concomitant migration of acyl groups. The reaction of 2,3,6,T,3, 4, 6 -hepta-0-acetylsucrose (21) and 2,3,4,6,1, 3, 4 -hepta-O-acetylsucrose (22) with diazomethane in dichloromethane in the presence of a catalytic proportion of boron trifluoride etherate for 0.5 h at —5° gave the corresponding 4-methyl (23) and 6 -methyl (24)... [Pg.243]


See other pages where Hydrides trifluoride, structure is mentioned: [Pg.172]    [Pg.80]    [Pg.271]    [Pg.104]    [Pg.605]    [Pg.921]    [Pg.25]    [Pg.120]    [Pg.82]    [Pg.96]    [Pg.140]    [Pg.386]   
See also in sourсe #XX -- [ Pg.27 , Pg.90 ]




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Hydrides structure

Trifluoride, structure

Trifluorides, structures

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