首页> 外文会议>日本化学会春季年会 >Synthesis of Oligosaccharide derived from Pathogenic E.coli UsingBoronic-Acid-Catalyzed Regio-and Stereoselective β-Rhamnosylation
【24h】

Synthesis of Oligosaccharide derived from Pathogenic E.coli UsingBoronic-Acid-Catalyzed Regio-and Stereoselective β-Rhamnosylation

机译:衍生自致胆酸催化的Regio-and StereoSelectiveβ-rhamnosation的源于致病大肠杆菌的寡糖的合成

获取原文

摘要

Pathogenic Escherichia coli (E.coli) O1 is the common bacterial pathogen infectingchickens,leading to substantial economic losses in the poultry industry worldwide.In addition,pathogenic E.coli O1 stains have zoonotic potential.Therefore,to elucidate of the minimalglycan epitopes of pathogenic E.coli O1 and develop the glycovaccines,the chemical synthesisof homogeneous and structurally well-defined partial oligosaccharides and theirglycoconjugates have attracted much attention.Herein,we report the efficient synthesis ofcomplex oligosaccharide derived from pathogenic E.coli O13) and its glycoconjugate usingrecently developed our boronic-acid-catalyzed regio-and stereoselective β-rhamnosylation asa key step.
机译:致病性大肠杆菌(大肠杆菌)O1是常见的细菌病原体感染性,导致禽类工业中的大量经济损失。此外,致病的大肠杆菌O1污渍具有动物源性。因此,为了阐明致病性的最小甘油表位大肠杆菌O1和发展甘油杂志,均匀和结构明确定义的部分寡糖和术术的化学合成引起了很多关注。Reeptin,我们报告了衍生自致病大肠杆菌O13的复合寡糖的有效合成)及其糖缀合物使用了我们的糖缀合物硼酸酸催化的Regio-and立体选择β-rhamnosylAsa键。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号