Synthesis of O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1→3)-O-β-D-galactopyranosyl-(1→4)-2-acetamido-2-deoxy-D- glucopyranose and two related trisaccharides containing the “lacto-N-biose II” unit
作者:Rexford L. Thomas、Rashmi Dubey、Saeed A. Abbas、Khushi L. Matta
DOI:10.1016/0008-6215(87)80251-3
日期:1987.11
Alternatively, bromide 1 was allowed to react with 2-acetamido-1,6-anhydro-3-O-benzyl-2-deoxy-beta-D-glucopyranose in 1:1 benzene-nitromethane in the presence of mercuric cyanide, followed by O-deacetylation, column chromatography, and reacetylation to give O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-beta-D- glucopyranosyl)-(1----3)-O-(2,4,6-tri-O-acetyl-beta-D-galactopyranosyl)- (1----4)-2-acetamido-1
3-O-(2-乙酰氨基-3,4,6-三-O-乙酰基-2-脱氧-β-D-吡喃葡萄糖基)-2,4,6-三-O-乙酰基-α-D-的缩合吡喃半乳糖基溴化物(1)与苄基2-乙酰氨基-3,6-二-O-苄基-2-脱氧-α-D-吡喃葡萄糖苷在沸腾的苯中并在氰化汞的存在下得到三糖,将其经O-去乙酰化,得到苄基O-(2-乙酰氨基-2-脱氧-β-D-吡喃葡萄糖基)-(1 ---- 3)-O-β-D-吡喃半乳糖基-(1 ---- 4)-3,6-di -O-苄基-2-脱氧-α-D-吡喃葡萄糖苷e,通过催化氢解裂解其苄基,得到标题三糖。或者,在氰化汞存在下,使溴化物1与2-乙酰氨基-1,6-脱水-3-O-苄基-2-脱氧-β-D-吡喃葡萄糖在1:1的苯硝基甲烷中反应,然后O-脱乙酰基,柱层析,再乙酰化,得到O-(2-acetamido-3,4,6-三-O-乙酰基-2-脱氧-β-D-吡喃葡萄糖基)-(1 ---- 3)-O-(2