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

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Thiosugars
Oligosaccharides
Sugars

Keywords

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

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

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

A new entry for the controlled synthesis of 2,6-dideoxy oligosaccharides. / Toshima, Kazunobu; Nozaki, Yuko; Inokuchi, Hatsuki; Nakata, Masaya; Tatsuta, Kuniaki; Kinoshita, Mitsuhiro.

In: Tetrahedron Letters, Vol. 34, No. 10, 05.03.1993, p. 1611-1614.

Research output: Contribution to journalArticle

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, vol. 34, no. 10, pp. 1611-1614. https://doi.org/10.1016/0040-4039(93)85021-N
Toshima, Kazunobu ; Nozaki, Yuko ; Inokuchi, Hatsuki ; Nakata, Masaya ; Tatsuta, Kuniaki ; Kinoshita, Mitsuhiro. / A new entry for the controlled synthesis of 2,6-dideoxy oligosaccharides. In: Tetrahedron Letters. 1993 ; Vol. 34, No. 10. pp. 1611-1614.
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