A simple procedure for the synthesis of the methyl and benzyl glycosides of Neu5Ac and 4-epi-Neu5Ac. Conversion of the benzyl and methyl glycosides of Neu5Ac into N-trifluoroacetylneuraminic acid benzyl glycosides

DOI: 10.1016/S0008-6215(92)84240-S

Source and publish data:

Carbohydrate Research p. 161 - 176 (1992)

Update date:2022-08-04

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Authors:

Byramova, Nargiz E.

Tuzikov, Alexander B.

Bovin, Nicolai V.

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Article abstract of DOI:10.1016/S0008-6215(92)84240-S

From the reaction products of the Kuhn-Bashang synthesis of Neu5Ac, 5-acetamido-3,5-dideoxy-α- and -β-D-glycero-D-talo-2-nonulopyranosonic acid (4-epi-Neu5Ac) were isolated as the acetylated methyl esters (1 and 2).Treatment of methyl (5-acetamido-4,7,8,9

Full text of DOI:10.1016/S0008-6215(92)84240-S

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Product name:methyl (benzyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-β-D-glycero-D-talo-2-nonulopyranosid)onate

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