p-methoxyphenyl 4,6-O-p-methoxyphenylbenzylidene-3-deoxy-3-C-(difluoromethylene)-β-D-xylo-hex-3-ulopyranoside 、
N-acetyl-4,7,8,9-tetra-O-benzyloxymethyl-2-deoxy-neuraminic acid 在
4-二甲氨基吡啶 、
盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下,
以
二氯甲烷 为溶剂,
反应 5.0h,
以72%的产率得到[(2S,4aR,6S,7R,8aR)-8-(difluoromethylidene)-6-(4-methoxyphenoxy)-2-(4-methoxyphenyl)-4a,6,7,8a-tetrahydro-4H-pyrano[3,2-d][1,3]dioxin-7-yl] (2S,4S,5R,6R)-5-acetamido-4-(phenylmethoxymethoxy)-6-[(1S,2R)-1,2,3-tris(phenylmethoxymethoxy)propyl]oxane-2-carboxylate