Partial synthesis of a sea cucumber ganglioside analogue from a starfish cerebroside

Ryuichi Higuchi, Takeshi Mori, Tetsuji Sugata, Koji Yamada, Tomofumi Miyamoto

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

A sea cucumber ganglioside analogue 7 (NGNAα2→6Glcβ1→1Cer), which contains a phytosphingosine as a long-chain base and an α-hydroxy fatty acid, has been synthesized. Coupling of the methyl 2-thioglycoside derivative 5 of N-glycolylneuraminic acid with a cerebroside derivative 3, prepared from acanthacerebroside A (1), afforded protected ganglioside analogue 6, which was deprotected to give the corresponding ganglioside 7.

Original languageEnglish
Pages (from-to)145-147
Number of pages3
JournalEuropean Journal of Organic Chemistry
Issue number1
Publication statusPublished - Jan 1 1999

Fingerprint

Cerebrosides
Gangliosides
phytosphingosine
analogs
fatty acids
synthesis
Thioglycosides
Derivatives
acids
Fatty Acids

All Science Journal Classification (ASJC) codes

  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

Partial synthesis of a sea cucumber ganglioside analogue from a starfish cerebroside. / Higuchi, Ryuichi; Mori, Takeshi; Sugata, Tetsuji; Yamada, Koji; Miyamoto, Tomofumi.

In: European Journal of Organic Chemistry, No. 1, 01.01.1999, p. 145-147.

Research output: Contribution to journalArticle

Higuchi, Ryuichi ; Mori, Takeshi ; Sugata, Tetsuji ; Yamada, Koji ; Miyamoto, Tomofumi. / Partial synthesis of a sea cucumber ganglioside analogue from a starfish cerebroside. In: European Journal of Organic Chemistry. 1999 ; No. 1. pp. 145-147.
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