Synthesis of L-glycero- and D-glycero-D-manno-Heptose Building Blocks for Stereoselective Assembly of the Lipopolysaccharide Core Trisaccharide of Vibrio parahemolyticus O2

被引:10
作者
Wang, Junchang [1 ]
Rong, Jingjing [1 ]
Lou, Qixin [1 ]
Zhu, Yirong [1 ]
Yang, You [1 ]
机构
[1] East China Univ Sci & Technol, Sch Pharm, Shanghai Key Lab New Drug Design, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
NEISSERIA-MENINGITIDIS LIPOPOLYSACCHARIDE; CHEMICAL-SYNTHESIS; CHAIN ELONGATION; NOVO SYNTHESIS; TETRASACCHARIDE; GLYCOSYLATION; OLIGOSACCHARIDES; BIOSYNTHESIS; HOMOLOGATION; DIVERSITY;
D O I
10.1021/acs.orglett.0c02961
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Synthesis of bacterial cell surface L-glycero-D-manno-heptose (L,D-Hep)- and D-glycero-D-manno-heptose (D,D-Hep)containing higher carbon sugars is a challenging task. Here, we report a convenient and efficient approach for the synthesis of the L,D-Hep and D,D-Hep building blocks. Using L-lyxose and D-ribose as starting materials, this approach features diastereoselective Mukaiyama-type aldol reactions as the key steps. On the basis of the synthetic L,D-Hep and D,D-Hep building blocks, we achieved the first stereoselective synthesis of the unique alpha-L,D-Hep-(1.3)-alpha-D,D-Hep-(1 5)-alpha-Kdo core trisaccharide of the lipopolysaccharide of Vibrio parahemolyticus O2.
引用
收藏
页码:8018 / 8022
页数:5
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