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- W1974822409 abstract "Starting from 1,2.5,6-di-O-isopropylidene-D-mannitol and -D-glucitol, respectively, D-threo- and erythro-hex-E-3-enitol were synthesized; these were hydrogenated to the 3,4-dideoxy compounds, which were converted into the corresponding 1,2:5,6-dianhydrides, possessing significantly different cytostatic activity. The D-threo- and erythro-E-3-ene diepoxides were also synthesized; they are unstable at room temperature and show no biological activity." @default.
- W1974822409 created "2016-06-24" @default.
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- W1974822409 date "1980-08-01" @default.
- W1974822409 modified "2023-09-23" @default.
- W1974822409 title "Synthesis of 1,2:5,6-dianhydro-3,4-dideoxy-erythro- and D-threo-hexitol and their E-3-ENE derivatives" @default.
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- W1974822409 doi "https://doi.org/10.1016/s0008-6215(00)85364-1" @default.
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