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

応用化学科

研究成果: Article › 査読

10 被引用数 (Scopus)

抄録

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.

本文言語	English
ページ（範囲）	27-29
ページ数	3
ジャーナル	Green Chemistry
巻	4
号	1
DOI	https://doi.org/10.1039/b109172g
出版ステータス	Published - 2002 1 1

ASJC Scopus subject areas

環境化学
汚染

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10.1039/b109172g

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引用スタイル

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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.",

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