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- W2023161712 abstract "Condensation of D-talose with nitromethane in alkaline methanol gave the corresponding epimeric 1-deoxy-1-nitroheptitols which were converted into D-glycero-L-altro-heptose and D-glycero-L-allo-heptose (1.5:1) in 44% yield. Reduction of D-glycero-L-altro-heptose with sodium borohydride gave the hitherto unknown meso-glycero-altro-heptitol. The gas–liquid chromatography retention times of the 10 geometrically isomeric heptitol heptaacetates were determined. These data provide the necessary information for the key step in a procedure for the rapid identification of an unknown heptose." @default.
- W2023161712 created "2016-06-24" @default.
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- W2023161712 date "1966-01-01" @default.
- W2023161712 modified "2023-09-30" @default.
- W2023161712 title "THE SYNTHESIS OF <scp>D</scp>-<i>glycero</i>-<scp>L</scp>-<i>altro</i>-HEPTOSE, <scp>D</scp>-<i>glycero</i>-<scp>L</scp>-<i>allo</i>-HEPTOSE, AND <i>meso</i>-<i>glycero</i>-<i>altro</i>-HEPTITOL" @default.
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- W2023161712 doi "https://doi.org/10.1139/v66-006" @default.
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