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- W2000435736 abstract "Abstract Oxidation of methyl α- and β- d -galactopyranoside with periodic acid in dimethyl sulphoxide gave, in each case, one major, monomeric product, isolated as a diacetate. These syrupy products were characterised by m.s. and 1 H- and 13 C-n.m.r. spectroscopy as (1 S ,2 S ,4 R ,7 S )-7-acetoxy-4-acetoxymethyl-2-methoxy-3,6,8-trioxabicyclo[3.2.1.]octane and (1 S ,2 R ,4 R ,7 S )-7-acetoxy-4-acetoxymethyl-2-methoxy-3,6,8-trioxabicyclo[3.2.1.]octane, respectively. Chemical shifts and coupling constants for the products were determined partly from the experimental n.m.r. spectra, and partly by an iterative fitting-procedure with the computer program NEMEN." @default.
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- W2000435736 date "1981-04-01" @default.
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- W2000435736 title "Characterisation by 1H- and 13C-n.m.r. spectroscopy of the products from oxidation of methyl α- and β-d-galactopyranoside with periodic acid in dimethyl sulphoxide" @default.
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- W2000435736 doi "https://doi.org/10.1016/s0008-6215(00)80985-4" @default.
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