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- W1965547467 abstract "1-O-Benzoyl-2,3:5,6-di-O-isopropylidene-d-gulitol (3) and -d-allitol (4) were found to be inert toward oxidation by chromium trioxide in pyridine, confirming previous findings of apparent effects of 1,4-interaction. 1-O-Benzoyl-2,3:5,6-di-O-isopropylidene-d-mannitol (2), though previously established to be inert toward chromium trioxide in pyridine, was smoothly oxidized to 6-O-benzoyl-1,2:4,5-di-O-isopropylidene-d-mannitol (2), though previously established to be inert toward chromium trioxide in pyridine, was smoothly oxidized to 6-O-benzoyl-1,2:4,5-di-O-isopropylidene-d-arabino-3-hexulose (5) by methyl sulfoxide in acetic anhydride. However, the latter converted 1,5-di-O-benzoyl-2,4-O-benzylidene-xylitol (6) and -ribitol (7) into 3-(methylthio)methyl ethers." @default.
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- W1965547467 date "1970-04-01" @default.
- W1965547467 modified "2023-09-23" @default.
- W1965547467 title "The effect of stereochemistry on the oxidation of substituted hexitols" @default.
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- W1965547467 doi "https://doi.org/10.1016/s0008-6215(00)84898-3" @default.
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