Synthetic Studies on Sialoglycoconjugates 104: Synthesis of Kdn-Lewis X Ganglioside Analogs Containing Modified Reducing Terminal and L-Rhamnose in Place of L-Fucose¹

1. Dedicated to the memory of Professor Akira Hasegawa.

²

2. For Part 103, see T. Ikami, T. Kakigami, K. Baba, H. Hamajima, T. Jomori, T. Usui, Y. Suzuki, H. Tanaka, H. Ishida, A. Hasegawa and M. Kiso, J. Carbohydr. Chem., in press.

Abstract

KDN-Le^x ganglioside analogs (10, 13, 16 and 19) containing the modified reducing terminal and L-rhamnose in place of L-fucose have been synthesized. Glycosidation of methyl 2,3,4-tri-O-benzyl-1-thio-α-L-rhamnopyranoside (1) with 2-(trimethylsilyl)ethyl O-(2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-(1→3)-O-(2,4,6-tri-O-benzyl-α-D-galacopyranoside (2), followed by reductive ring opening of the benzylidene acetal, gave 2-(trimethylsilyl)ethyl O-(2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1→3)-O-(2-acet-amido-6-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1→3)-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1→4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside (4). The tetrasaccharide 4 was coupled with methyl O-(methyl 4,5,7,8,9-penta-O-acetyl-3-deoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-(2→3)-2,4,6-tri-O-benzoyl-1-thio-β-D-galactopyranoside(5), using dimethyl(methylthio)sulfonium triflate (DMTST), to give the hexasaccharide 6, which was converted into compound 11 in the usual manner. Compounds 8 and 11 were transformed, via bromination of the reducing terminal, radical reduction, O-deacylation and saponification of the methyl ester, into the desired KDN-Le^x hexasaccharides (10, 13). On the other hand, glycosylation of 2-(tetradecyl)hexadecanol with α-trichloroacetimidates 14 and 17, afforded the target ganglioside analogs 16 and 19.

1. Dedicated to the memory of Professor Akira Hasegawa.

2. For Part 103, see T. Ikami, T. Kakigami, K. Baba, H. Hamajima, T. Jomori, T. Usui, Y. Suzuki, H. Tanaka, H. Ishida, A. Hasegawa and M. Kiso, J. Carbohydr. Chem., in press.

Notes

1. Dedicated to the memory of Professor Akira Hasegawa.

2. For Part 103, see T. Ikami, T. Kakigami, K. Baba, H. Hamajima, T. Jomori, T. Usui, Y. Suzuki, H. Tanaka, H. Ishida, A. Hasegawa and M. Kiso, J. Carbohydr. Chem., in press.

Dedicated to the memory of Professor Akira Hasegawa