Synthesis ofβ-D-Ribofuranosyl-(1→3)-α-L-rhamnopyranosyl-(1→3)-L-rhamnopyranose by in situ Activating Glycosylation Using 1-OH Sugar Derivative and Me3SiBr–CoBr2–Bu4NBr–Molecular Sieves 4A System-Reference-Cited by-同舟云学术

Synthesis ofβ-D-Ribofuranosyl-(1→3)-α-L-rhamnopyranosyl-(1→3)-L-rhamnopyranose by in situ Activating Glycosylation Using 1-OH Sugar Derivative and Me3SiBr–CoBr2–Bu4NBr–Molecular Sieves 4A System

Published:2001-09 Issue:9 Volume:74 Page:1679-1694
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Hirooka Motoko,Mori Yoko,Sasaki Akiko,Koto Shinkiti,Shinoda Yoshika,Morinaga Aya

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference117 articles.

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2. Glycosylation via locked anomeric configuration: stereospecific synthesis of oligosaccharides containing the β-d-mannopyranosyl and β-l-rhamnopyranosyl linkage11For a preliminary account of this work, see ref. [7].

3. Direct synthesis of β-d-Xyl-(1→2)-β-d-Man-(1→4)-α-d-Glc-OME: a trisaccharide component of the Hyriopsis schlegelii glycosphingolipid

4. First synthesis of anomeric sulfimides - efficient glycosyl donors

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