Synthesis of 2-Amino-2,5-dideoxy-5-hydroxyphosphinyl-D-mannopyranose Derivatives: New Phospho-sugar Analogues of D-Mannosamine

Tadashi Hanaya, Yasushi Fujii, Hiroshi Yamamoto

    Research output: Contribution to journalArticlepeer-review

    3 Citations (Scopus)

    Abstract

    3,6-Di-O-benzyl-5-deoxy-5-dimethylphosphinyi-1,2-0-isopropylidene-α- D-glucofuranose 5 was converted, in four steps, into methyl 2-acetamido-3,6-di-O-benzyl-2,5-dideoxy-5-dimethoxyphosphinyl-α-D- mannofuranoside 7, which led to 3,5-di-O-benzyl derivatives 9 of a P-in-the-ring D-mannosamine analogue.

    Original languageEnglish
    Pages (from-to)790-791
    Number of pages2
    JournalJournal of Chemical Research - Part S
    Issue number12
    DOIs
    Publication statusPublished - Jan 1 1998

    ASJC Scopus subject areas

    • Chemistry(all)

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