Synthesis of a thio-linked Lewis A (Le(a)) epitope

The synthesis of heptyl (alpha-L-fucopyransoyl)-(1-->4)-S-[(beta-D-galactopyranosyl)-(1--> 3)] -1,4-dithio-beta-D-glucopyranoside (2), as thio-linked Lewis A analogue was based on thexyldimethylsilyl 3-O-allyl-2-O-benzoyl-6-O-(4-methoxybenzyl)-4-thio-beta-D-glucopyranosid e (15) which was readily obtained from D-galactose. Reaction of 15 with O-3,4-di-O-acetyl-2-O-(4-methoxybenzyl)-alpha-L-fucopyranosyl trichloroacetimidate (8) as fucosyl donor afforded the alpha-(1-->4)-thio-linked disaccharide. Replacement of the 4-methoxybenzyl groups by acetyl groups and removal of the 3a-O-allyl group afforded as 3a-O-unprotected acceptor thexyldimethylsilyl (2,3,4-tri-O-acetyl-alpha-L-fucopyranosyl)-(1-->4)-S-6-O-acetyl-2-O-benz oyl -4-thio-beta-D-glucopyranoside (19), which gave with 2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranosyl trichloroacetimidate as galactosyl donor (20) the trisaccharide. Transformation into a trichloroacetimidate as glycosyl donor, glycosylation of heptylmercaptan, and then removal of the O-acyl protective groups afforded target molecule 2.