Carbonic acid allyl ester (2S,3S,4R)-2,3,4-tris-benzyloxy-4-hydroxy-butyl ester 、
2,4-Di-O-acetyl-3-O-<2,4,6-tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl)-α-D-glucopyranosyl>-α-L-rhamnopyranosyl trichloroacetimidate 在
三氟甲磺酸三甲基硅酯 、 4 A molecular sieve 作用下,
以
二氯甲烷 为溶剂,
反应 0.08h,
以91%的产率得到1-O-Allyloxycarbonyl-2,3,5-tri-O-benzyl-4-O-<2,4-di-O-acetyl-3-O-<2,4,6-tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl)-α-D-glucopyranosyl>-α-L-rhamnopyranosyl>-D-ribitol