Synthesis of sialyl lewis X ganglioside analogues containing modified l-fucose residues
作者:Akira Hasegawa、Mitsutoshi Kato、Takashi Ando、Hideharu Ishida、Makoto Kiso
DOI:10.1016/0008-6215(95)00135-g
日期:1995.9
Sialyl Le(x) ganglioside analogues containing 2-epi-, 2,3-di-epi-, 4-epi-, and 2-O-methyl-L-fucose in place of the L-fucose residue have been synthesized. Glycosylation of 2-(trimethylsilyl)ethyl O-(2-acetamido-4,6-O-benzylidene-2-deoxy-beta-D-glucopyranosyl)-(1-->3)- 2,4,6- tri-O-benzyl-beta-D-galactopyranoside with the methyl 1-thioglycoside derivatives of the respective fucose analogues, using
合成了代替L-岩藻糖残基的包含2-epi-,2,3-二-epi-,4-epi-和2-O-甲基-L-岩藻糖的唾液酸Le(x)神经节苷脂类似物。2-(三甲基甲硅烷基)乙基O-(2-乙酰氨基-4,6-O-亚苄基-2-脱氧-β-D-吡喃葡萄糖基)-(1-> 3)-2,4,6-三- O-苄基-β-D-吡喃半乳糖苷与相应岩藻糖类似物的甲基1-硫代糖苷衍生物一起使用二甲基(甲硫基)tri三氟甲磺酸盐(DMTST)作为促进剂,得到了相应的受保护的2-(三甲基甲硅烷基)乙基脱氧α- L-己吡喃糖基-(1→3)-O-(2-乙酰氨基-2-脱氧β-D-吡喃吡喃糖基)-(1→3)-β-D-吡喃半乳糖苷。这些通过其亚苄基缩醛基的还原性开环转化为糖基受体。这些化合物与甲基O-(甲基5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-D-glycero-alpha-D-半乳糖-2-壬基吡喃半乳糖酸酯)-(2->