Synthesis ofO-β-D-Glucopyranosyl-(1→2)-O-β-D-glucopyranosyl-(1→6)-D-glucopyranose; Dehydrative β-D-Glucosylation Using 2-O-Acetyl-3,4,6-tri-O-benzyl-D-glucopyranose-Reference-Cited by-同舟云学术

Synthesis ofO-β-D-Glucopyranosyl-(1→2)-O-β-D-glucopyranosyl-(1→6)-D-glucopyranose; Dehydrative β-D-Glucosylation Using 2-O-Acetyl-3,4,6-tri-O-benzyl-D-glucopyranose

Published:1985-01 Issue:1 Volume:58 Page:120-122
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Koto Shinkiti,Morishima Naohiko,Sato Hiroko,Sato Yuko,Zen Shonosuke

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/58/1/58_1_120/_pdf

Reference14 articles.

1. The Glucosylation of Several Alcohols with Tetra-O-benzyl-α-D-glucopyranose and a Mixture ofp-Nitrobenzenesulfonyl Chloride, Silver Trifluoromethanesulfonate, and Triethylamine

2. One-stage glycosylation using protected glycose: the synthesis of O-β-D-glucopyranosyl-(1 → 3)-O-[β-D-glucopyranosyl-(1 → 6)]-D-glucopyranose

3. The use of 2-O-acyl-1-O-sulfonyl-d-galactopyranose derivatives in β-d-galactopyranoside synthesis

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