A highly stereoselective synthesis of β-olivosides by glycosidations of 2-iodo-olivosyl fluoride using montmorillonite K-10 as an environmentally benign solid acid

Kazunobu Toshima, Keizou Uehara, Hideyuki Nagai, Shuichi Matsumura

Research output: Contribution to journalArticle

9 Citations (Scopus)


The novel and highly β-stereoselective glycosidations of a 2-iodo-olivosyl fluoride and alcohols using a heterogeneous and environmentally benign solid acid, montmorillonite K-10, have been developed to afford the corresponding 2-iodo-β-olivosides in high yields with high stereoselectivities.

Original languageEnglish
Pages (from-to)27-29
Number of pages3
JournalGreen Chemistry
Issue number1
Publication statusPublished - 2002 Jan 1


ASJC Scopus subject areas

  • Environmental Chemistry
  • Pollution

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