SYNTHESIS OF 6-O-(5-ACETAMIDO-3,5-DIDEOXY-α-D-glycero-D-galacto-2-NONULOPYRANOSYLONIC ACID)-D-GALACTOSE

DOI: 10.1016/S0008-6215(00)82584-7

Source and publish data:

Carbohydrate Research p. 221 - 234 (1982)

Update date:2022-09-26

Topics:

Authors:

Vleugel, Dominicus J. M. van der

Wassenburg, Fred R.

Zwikker, Jan W.

Vliegenthart, Johannes F. G.

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Article abstract of DOI:10.1016/S0008-6215(00)82584-7

Condensation of methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-2-chloro-2,3,5-trideoxy-β-D-glycero-D-galacto-2-nonulopyranosonate with benzyl 2,3,4-tri-O-benzyl-β-D-galactopyranoside, using silver salicylate as promoter, gave benzyl 2,3,4-tri-O-benzyl-6-O-(methyl-5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-α-D-glycero-D-galacto-2-nonulopyranosylonate)-β-D-galactopyranoside (11) as the main product in 65percent yield.Furthermore, the following by-products were formed: methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-O-salicyloyl-D-glycero-D-galacto-2-nonulopyranosonate, methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-2,6-anhydro-3,5-dideoxy-D-glycero-D-galacto-non-2-enopyranosonate, and an impure compound that gave, after O-deacetylation and catalytic hydrogenolysis, 6-O-(methyl 5-acetamido-3,5-dideoxy-β-D-glycero-D-galacto-2-nonulopyranosylonate)-D-galactose.O-Deacetylation of 11 gave benzyl 2,3,4-tri-O-benzyl-6-O-(methyl 5-acetamido-3,5-dideoxy-α-D-glycro-D-galacto-2-nonulopyranosylonate)-β-D-galactopyranoside, which was converted into 6-O-(methyl 5-acetamido-3,5-dideoxy-α-D-glycero-D-galacto-2-nonulopyranosylonate)-D-galactose (13) by catalytic hydrogenolysis.Saponification of 13 gave the title compound as its potassium salt.