Syntheses ofO-β-D-Mannosyl-(1→4)-O-α-D-mannosyl-(1→3)-L-rhamnose andO-(2-Acetamido-2-deoxy-β-D-mannosyl)-(1→4)-O-α-D-galactosyl-(1→4)-D-galactose via In-situ-activating Glycosylation Using 2-O-Acetyl-3,4,6-tri-O-benzyl-D-glucose-Reference-Cited by-同舟云学术

Syntheses ofO-β-D-Mannosyl-(1→4)-O-α-D-mannosyl-(1→3)-L-rhamnose andO-(2-Acetamido-2-deoxy-β-D-mannosyl)-(1→4)-O-α-D-galactosyl-(1→4)-D-galactose via In-situ-activating Glycosylation Using 2-O-Acetyl-3,4,6-tri-O-benzyl-D-glucose

Published:2003-08 Issue:8 Volume:76 Page:1603-1615
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Koto Shinkiti,Shinoda Yoshika,Hirooka Motoko,Sekino Akiko,Ishizumi Sachiko,Koma Mutsuko,Matuura Chieko,Sakata Naoko

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference77 articles.

1. 2-Oxo- and 2-Oximinoglycosyl Halides: Versatile Glycosyl Donors for the Construction of .BETA.-D-Mannose and .BETA.-D-Mannosamine-containing Oligosaccharides.

2. Reaction d'imidates de glucopyranosyle avec l'acetonitrile. Applications synthetiques

3. Synthesis of β-O-glycosides using enol ether and imidate derived leaving groups. Emphasis on the use of nitriles as a solvent

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