Synthetic studies on novel fucosylated glycosphingolipids from the millipede, Parafontaria laminata armigera

Noriyasu Hada, Isao Ohtsuka, Mutsumi Sugita, Tadahiro Takeda

Research output: Contribution to journalArticlepeer-review

18 Citations (Scopus)

Abstract

A novel glycosphingolipid, β-D-Manp-(1→4)-[(α-L-Fucp-(1→3)]-β-D-Glcp-(1→1)-Cer, from the millipede, Parafontaria laminata armigera, was synthesized. A key reaction of this synthetic procedure is the formation of a spiro-orthoester and its reduction for β-selective mannosylation. (C) 2000 Elsevier Science Ltd.

Original languageEnglish
Pages (from-to)9065-9068
Number of pages4
JournalTetrahedron Letters
Volume41
Issue number47
DOIs
Publication statusPublished - 2000 Nov 18

Keywords

  • Chemical synthesis
  • Glycosphingolipids
  • Parafontaria laminata armigera

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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