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

doi:10.1039/b109172g

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

Department of Applied Chemistry

Research output: Contribution to journal › Article › peer-review

10 Citations (Scopus)

Abstract

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 language	English
Pages (from-to)	27-29
Number of pages	3
Journal	Green Chemistry
Volume	4
Issue number	1
DOIs	https://doi.org/10.1039/b109172g
Publication status	Published - 2002 Jan 1

ASJC Scopus subject areas

Environmental Chemistry
Pollution

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

Abstract

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