The use of 2,6-anhydro-2-thio glycopyranosyl fluoride for a highly α-stereoselective glycosylation

Kazunobu Toshima, Satsuki Mukaiyama, Takashi Ishiyama, Kuniaki Tatsuta

Research output: Contribution to journalArticle

19 Citations (Scopus)


The glycosylation of 2, 6-anhydro-1-f1uoro-2-thioglycoside 1 with alcohols under various conditions proceeded smoothly at low temperature to give the corresponding α-glycosides in high yields, and the selectivity was highly independent on the conditions examined.

Original languageEnglish
Pages (from-to)6361-6362
Number of pages2
JournalTetrahedron Letters
Issue number44
Publication statusPublished - 1990


ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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