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- W1971082482 abstract "Abstract Simple analogues of the dialdehyde formed by periodate oxidation of benzyl β- L -arabinopyranoside have been prepared. Oxydiacetaldehyde may be condensed with one or two moles of substituted thiosemicarbazides, whereas N -aryliminodiacetaldehydes give only bis(thiosemicarbazones). The oxidation of N -arylpyrrolidine-3,4-diols with one equivalent of periodate is straightforward if electron-attracting aromatic substituents are present, but, otherwise, some cleavage of NC bonds in the pyrrolidine ring can be demonstrated. The crystalline hemialdal, 2,6-dihydroxy-4-phenylmorpholine, was isolated. The rates of conversion of some α-functionally-substituted thiosemicarbazones into glyoxal derivatives have been compared." @default.
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- W1971082482 date "1968-07-01" @default.
- W1971082482 modified "2023-10-16" @default.
- W1971082482 title "The reaction of the periodate-oxidation products of 1,4-anhydroerythritol and of some related pyrrolidine glycols with thiosemicarbazides" @default.
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- W1971082482 doi "https://doi.org/10.1016/s0008-6215(00)81203-3" @default.
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