A new entry for the controlled synthesis of 2,6-dideoxy oligosaccharides

Kazunobu Toshima, Yuko Nozaki, Hatsuki Inokuchi, Masaya Nakata, Kuniaki Tatsuta, Mitsuhiro Kinoshita

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

A novel methodology for the controlled synthesis of 2,6-dideoxy oligosaccharides by combinational use of an activated 2,6-anhydro-2-thio sugar and a deactivated 2,6-anhydro-2-sulfinyl sugar, both of which have a same leaving group at anomeric position, has been demonstrated.

Original languageEnglish
Pages (from-to)1611-1614
Number of pages4
JournalTetrahedron Letters
Volume34
Issue number10
DOIs
Publication statusPublished - 1993 Mar 5

Keywords

  • 2
  • 6-anhydro-2-sulfinyl sugar
  • 6-anhydro-2-thio sugar
  • avermectins.
  • glycosylation
  • oligosaccharide

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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    Toshima, K., Nozaki, Y., Inokuchi, H., Nakata, M., Tatsuta, K., & Kinoshita, M. (1993). A new entry for the controlled synthesis of 2,6-dideoxy oligosaccharides. Tetrahedron Letters, 34(10), 1611-1614. https://doi.org/10.1016/0040-4039(93)85021-N