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ChemInform Abstract: Synthesis of a Thio-Analogue of Lewis X by Regioselective Opening of Cyclic Sulfamidates.

✍ Scribed by B. AGUILERA; A. FERNANDEZ-MAYORALAS

Publisher
John Wiley and Sons
Year
2010
Weight
28 KB
Volume
29
Category
Article
ISSN
0931-7597

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✦ Synopsis

Synthesis of a Thio-Analogue of Lewis X by Regioselective Opening of Cyclic Sulfamidates.

-The synthesis of the title analogue (I) contains linking of galactose and allosamine, protected by a p-methoxyphenyl group at O-6 (higher yield), transformation into cyclic sulfamidate, and its regioselective opening with fucose 1-thiolate.

-(AGUILERA, B.;

πŸ“œ SIMILAR VOLUMES

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✍ T. EISELE; R. R. SCHMIDT πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 23 KB πŸ‘ 2 views

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