Environmentally benign and stereoselective formation of β-O-glycosidic linkages using benzyl-protected glucopyranosyl phosphite and montmorillonite K-10

Hideyuki Nagai, Shuichi Matsumura, Kazunobu Toshima

研究成果: Article査読

26 被引用数 (Scopus)

抄録

An environmentally benign and highly stereoselective β-glucopyranosylation without neighboring group participation has been developed employing benzyl-protected glucopyranosyl diethyl phosphite as a glycosyl donor and montmorillonite K-10 as an activator.

本文言語English
ページ(範囲)847-850
ページ数4
ジャーナルTetrahedron Letters
43
5
DOI
出版ステータスPublished - 2002 1 28

ASJC Scopus subject areas

  • 生化学
  • 創薬
  • 有機化学

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「Environmentally benign and stereoselective formation of β-O-glycosidic linkages using benzyl-protected glucopyranosyl phosphite and montmorillonite K-10」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

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