A Stereoselective One-stage α-Glucosylation with 2,3,4,6-Tetra-O-benzyl-α-D-glucopyranose and a Mixture of Methanesulfonic Acid, Cobalt(II) Bromide, and Tetraethylammonium Perchlorate-Reference-Cited by-同舟云学术

A Stereoselective One-stage α-Glucosylation with 2,3,4,6-Tetra-O-benzyl-α-D-glucopyranose and a Mixture of Methanesulfonic Acid, Cobalt(II) Bromide, and Tetraethylammonium Perchlorate

Published:1982-05 Issue:5 Volume:55 Page:1543-1547
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Koto Shinkiti,Morishima Naohiko,Zen Shonosuke

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/55/5/55_5_1543/_pdf

Reference19 articles.

1. The use of 1-O-tosyl-d-glucopyranose derivatives in α-d-glucoside synthesis

2. The mechanism of, and the solvent effects in, the glycosidation of D-glucosyl chlorides having a non-participating group at C-2, using silver perchlorate as catalyst

3. Halide ion catalyzed glycosidation reactions. Syntheses of .alpha.-linked disaccharides

4. A novel synthesis of 1,2-cis-disaccharides

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