Environmentally benign aryl C-glycosidations of unprotected sugars using montmorillonite K-10 as a solid acid

Kazunobu Toshima; Yasunobu Ushiki; Goh Matsuo; Shuichi Matsumura

doi:10.1016/S0040-4039(97)01724-3

Environmentally benign aryl C-glycosidations of unprotected sugars using montmorillonite K-10 as a solid acid

Kazunobu Toshima, Yasunobu Ushiki, Goh Matsuo, Shuichi Matsumura

Department of Applied Chemistry

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

21 Citations (Scopus)

Abstract

Highly practical aryl C-glycosidations of unprotected 1-OMe and 1-OH sugars with phenol and naphthol derivatives were effectively realized using montmorillonite K-10 as an environmentally compatible solid acid in CHCl₃ or H₂O.

Original language	English
Pages (from-to)	7375-7378
Number of pages	4
Journal	Tetrahedron Letters
Volume	38
Issue number	42
DOIs	https://doi.org/10.1016/S0040-4039(97)01724-3
Publication status	Published - 1997 Oct 20

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(97)01724-3

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abstract = "Highly practical aryl C-glycosidations of unprotected 1-OMe and 1-OH sugars with phenol and naphthol derivatives were effectively realized using montmorillonite K-10 as an environmentally compatible solid acid in CHCl3 or H2O.",

author = "Kazunobu Toshima and Yasunobu Ushiki and Goh Matsuo and Shuichi Matsumura",

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AU - Toshima, Kazunobu

AU - Ushiki, Yasunobu

AU - Matsuo, Goh

AU - Matsumura, Shuichi

PY - 1997/10/20

Y1 - 1997/10/20

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AB - Highly practical aryl C-glycosidations of unprotected 1-OMe and 1-OH sugars with phenol and naphthol derivatives were effectively realized using montmorillonite K-10 as an environmentally compatible solid acid in CHCl3 or H2O.

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Environmentally benign aryl C-glycosidations of unprotected sugars using montmorillonite K-10 as a solid acid

Abstract

ASJC Scopus subject areas

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