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- W2950586645 endingPage "7037" @default.
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- W2950586645 abstract "4-Deoxy-l-hexoses were synthesized starting from our previously reported reagent 1 and (R)-benzyl glycidyl ether, which led in few steps to a substituted dihydropyran 6. The stereocontrolled hydroxylation of the latter afforded the corresponding 4-deoxy-l-hexoses 7a, 9, and 11. The same procedure, starting from (S)-benzyl glycidyl ether, enabled the preparation of their d-series enantiomers." @default.
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- W2950586645 date "2004-09-10" @default.
- W2950586645 modified "2023-09-23" @default.
- W2950586645 title "Synthesis of 4-Deoxy-<scp>l</scp>-(and <scp>d</scp>-)hexoses from Chiral Noncarbohydrate Building Blocks" @default.
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- W2950586645 doi "https://doi.org/10.1021/jo0493774" @default.
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