STEREOSELECTIVITY OF GLYCOSYLATION WITH DERIVATIVES OF 2-AZIDO-2-DEOXY-D-GALACTOPYRANOSE. THE SYNTHESIS OF A DETERMINANT OLIGOSACCHARIDE RELATED TO BLOOD-GROUP A (TYPE 1)

DOI: 10.1016/0008-6215(83)88263-9

Source and publish data:

Carbohydrate Research p. 23 - 36 (1983)

Update date:2022-08-05

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Authors:

Bovin, Nikolai V.

Zurabyan, Sergei E.

Khorlin, Anatoly Ya.

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Article abstract of DOI:10.1016/0008-6215(83)88263-9

The stereoselective glycosylation of a model alcohol (cyclohexanol) by derivatives of 2-azido-2-deoxy-D-galactopyranose was studied under various conditions. 2-Azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-galactopyranosyl chloride (9) was found to be the most eff

Full text of DOI:10.1016/0008-6215(83)88263-9

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