A new approach toC-branched monosaccharides by the stereoselective hydrodesulfurization of methyl 4,6-O-benzylidene-3-[bis(methylthio)-methylene]-3-deoxy-α-D-erythro-hexopyranosid-2-ulose-Reference-Cited by-同舟云学术

A new approach toC-branched monosaccharides by the stereoselective hydrodesulfurization of methyl 4,6-O-benzylidene-3-[bis(methylthio)-methylene]-3-deoxy-α-D-erythro-hexopyranosid-2-ulose

Published:1995-09 Issue:9 Volume:1995 Page:1633-1636
ISSN:0947-3440
Container-title:Liebigs Annalen
language:de
Short-container-title:Liebigs Ann.

Author:

Peseke Klaus,Thiele Gabriela,Michalik Manfred

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,General Chemistry

Reference27 articles.

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4. The chemistry of castanospermine, part I: synthetic modifications at C-6

5. , , , , , J. Chem. Soc., Perkin Trans. 1, 1979, 2313–2316;

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. ChemInform Abstract: A New Approach to C-Branched Monosaccharides by the Stereoselective Hydrodesulfurization of Methyl 4,6-O-Benzylidene-3-(bis(methylthio) methylene)-3-deoxy-α-D-erythro-hexopyranosid-2-ulose.;ChemInform;2010-08-16

2. An Unusual C-1C-2 Ring-Splitting of Pyranosides by a Retro-Aldol Reaction - a Route to New Chiral Building Blocks;Liebigs Annalen;2006-01-25

3. Synthesis of Heteroanellated Pyranosides Starting from Methyl 4,6‐O‐benzylidene‐2,3‐dideoxy‐α‐d‐erythro‐hexopyranosid‐2‐ylidenemalononitrile;Journal of Carbohydrate Chemistry;2006-01-01

4. Synthesis of Pyrano‐ and Pyrido‐Anellated Pyranosides as Precursors for Nucleoside Analogues;Journal of Carbohydrate Chemistry;2005-04-01

5. Synthesis of Novel Anellated Pyranosides as Precursors of C‐Nucleoside Analogues Using Isopropyl 6‐O‐Acetyl‐3‐deoxy‐4‐S‐ethyl‐4‐thio‐α‐D‐threo‐hexopyranosid‐2‐ulose;Journal of Carbohydrate Chemistry;2004-12-27