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 journalArticle

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
Publication statusPublished - 1998

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Mannose
Sugars
Derivatives
mannosamine
propylene

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Synthesis of 2-Amino-2,5-dideoxy-5-hydroxyphosphinyl-D-mannopyranose Derivatives : New Phospho-sugar Analogues of D-Mannosamine. / Hanaya, Tadashi; Fujii, Yasushi; Yamamoto, Hiroshi.

In: Journal of Chemical Research - Part S, No. 12, 1998, p. 790-791.

Research output: Contribution to journalArticle

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