Para-Chlorobenzyl protecting groups as stabilizers of the glycosidic linkage: Synthesis of the 3-O-Sulfated lewis X trisaccharide

DOI: 10.1016/S0040-4039(97)01670-5

Source and publish data:

Tetrahedron Letters p. 6985 - 6988 (1997)

Update date:2022-08-03

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Authors:

Pohl, Nicola L.

Kiessling, Laura L.

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Article abstract of DOI:10.1016/S0040-4039(97)01670-5

Thr 3'O-sulfated trisacchande Lewis x (1) and unsulfated Lewis x (2) have been synthesized using a route that highlights a more facile regio selective benzylidene ring-opening procedure and the employment of chlorobenzyl groups as a way of strengthening the acid-labile α-fucose linkage.

Full text of DOI:10.1016/S0040-4039(97)01670-5

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