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

Noriyasu Hada, Isao Ohtsuka, Mutsumi Sugita, Tadahiro Takeda

Research output: Contribution to journalArticle

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
Publication statusPublished - 2000 Nov 18

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Glycosphingolipids

Keywords

  • Chemical synthesis
  • Glycosphingolipids
  • Parafontaria laminata armigera

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Synthetic studies on novel fucosylated glycosphingolipids from the millipede, Parafontaria laminata armigera. / Hada, Noriyasu; Ohtsuka, Isao; Sugita, Mutsumi; Takeda, Tadahiro.

In: Tetrahedron Letters, Vol. 41, No. 47, 18.11.2000, p. 9065-9068.

Research output: Contribution to journalArticle

Hada, N, Ohtsuka, I, Sugita, M & Takeda, T 2000, 'Synthetic studies on novel fucosylated glycosphingolipids from the millipede, Parafontaria laminata armigera', Tetrahedron Letters, vol. 41, no. 47, pp. 9065-9068.
Hada, Noriyasu ; Ohtsuka, Isao ; Sugita, Mutsumi ; Takeda, Tadahiro. / Synthetic studies on novel fucosylated glycosphingolipids from the millipede, Parafontaria laminata armigera. In: Tetrahedron Letters. 2000 ; Vol. 41, No. 47. pp. 9065-9068.
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