Bulletin of the Chemical Society of Japan p. 2535 - 2537 (1984)
Update date:2022-08-02
Topics:
Yoshimura
Yasumori
Kondo
Sato
The compound was stereoselectively synthesized from methyl 2,6-dideoxy-4-O-methyl- beta -L-threo-hexopyranosid-3-ulose through the successive conversions; cyanomesylation, reductive spiro aziridine formation, reductive ring-opening to the methyl-branched amino sugar, oxidation to the corresponding nitro sugar.
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