Bibliographic Details
| Title: |
Synthesis of the 6-deoxytalose-containing tri- and hexasaccharides of the O-antigen polysaccharide from Mesorhizobium huakuii IFO15243T |
| Authors: |
Zong, Guanghui1, Feng, Yichen1, Liang, Xiaomei1, Chen, Liezhong2, Zhang, Jianjun1 zhangjianjun@cau.edu.cn, Wang, Daoquan1 |
| Source: |
Carbohydrate Research. Sep2010, Vol. 345 Issue 14, p2067-2073. 7p. |
| Subjects: |
Oligosaccharides, Organic synthesis, Antigens, Polysaccharides, Bacteria, Glycosylation, Monomers, Glycoconjugates |
| Abstract: |
Abstract: The synthesis of a trisaccharide and a hexasaccharide, the monomer and dimer of the repeating unit of O-antigen polysaccharide from Mesorhizobium huakuii IFO15243, has been accomplished through suitable protecting group manipulations and stereoselective glycosylation reactions starting from commercially available l-rhamnose. The target oligosaccharides in the form of their p-methoxyphenyl glycosides are suitable for further glycoconjugate formation via selective cleavage of this group. [ABSTRACT FROM AUTHOR] |
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| Database: |
Engineering Source |
