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4-(吡啶-2-基)噻唑-2-基硫代糖苷作为通过暂时失活进行寡糖合成的双齿配体。

4-(pyridin-2-yl)thiazol-2-yl thioglycosides as bidentate ligands for oligosaccharide synthesis via temporary deactivation.

作者信息

Pornsuriyasak Papapida, Rath Nigam P, Demchenko Alexei V

机构信息

Department of Chemistry and Biochemistry, University of Missouri-St. Louis, St. Louis, Missouri 63121, USA.

出版信息

Chem Commun (Camb). 2008 Nov 21(43):5633-5. doi: 10.1039/b810569c. Epub 2008 Oct 1.

DOI:10.1039/b810569c
PMID:18997976
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3150469/
Abstract

This study focusses on a new concept for oligosaccharide synthesis based on 4-(pyridin-2-yl)thiazol-2-yl thioglycosides that can either act as effective glycosyl donors or can be deactivated by stable bidentate complexation with palladium(II) bromide.

摘要

本研究聚焦于基于4-(吡啶-2-基)噻唑-2-基硫代糖苷的寡糖合成新概念,该硫代糖苷既可以作为有效的糖基供体,也可以通过与溴化钯(II)形成稳定的双齿络合物而失活。

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引用本文的文献

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S-Benzimidazolyl glycosides as a platform for oligosaccharide synthesis by an active-latent strategy.S-苯并咪唑基糖苷作为通过活性-潜伏策略进行寡糖合成的平台。

本文引用的文献

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Glycans in cancer and inflammation--potential for therapeutics and diagnostics.癌症与炎症中的聚糖——治疗与诊断潜力
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