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- W1995980162 abstract "7-Deoxy-7-iodohept-1-enitols react intramolecularly to give 5-carba analogues of pyranoses (pseudo sugars) by the action of tributyltin hydride, which generates a radical at C-7. The configuration at the new chiral centre depends on the relative orientation of the oxygen functions in the starting material and the pattern of substitution." @default.
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- W1995980162 date "1992-03-01" @default.
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- W1995980162 title "Radical cyclisation of hept-1-enitols" @default.
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- W1995980162 doi "https://doi.org/10.1016/0008-6215(92)84055-w" @default.
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