Nishi Nobuya, Nashida Junki, Kaji Eisuke, Takahashi Daisuke, Toshima Kazunobu
Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan.
Chem Commun (Camb). 2017 Mar 9;53(21):3018-3021. doi: 10.1039/c7cc00269f.
Regio- and stereoselective β-mannosylations using 1,2-anhydromannose and diol sugar acceptors in the presence of a boronic acid catalyst proceeded smoothly to give the corresponding β-mannosides with high regio- and β-stereoselectivities in high yields without further additives under mild conditions. In addition, this glycosylation method was applied successfully to the synthesis of a tetrasaccharide repeating unit of lipopolysaccharide (LPS) derived from E. coli O75.
在硼酸催化剂存在下,使用1,2-脱水甘露糖和二醇类糖受体进行区域和立体选择性β-甘露糖基化反应,反应顺利进行,在温和条件下无需进一步添加物,即可高产率地得到具有高区域和β-立体选择性的相应β-甘露糖苷。此外,这种糖基化方法已成功应用于大肠杆菌O75来源的脂多糖(LPS)四糖重复单元的合成。