Highly Stereoselective Synthesis of Primary, Secondary, and Tertiary α-S-Sialosides under Lewis Acidic Conditions-Reference-Cited by-同舟云学术

Highly Stereoselective Synthesis of Primary, Secondary, and Tertiary α-S-Sialosides under Lewis Acidic Conditions

Published:2012-07-30 Issue:16 Volume:14 Page:4138-4141
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Noel Amandine¹,Delpech Bernard¹,Crich David¹

Affiliation:

1. Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles, CNRS, 1 Avenue de la Terrasse, 91190 Gif-sur-Yvette, France, and Department of Chemistry, Wayne State University, Detroit, Michigan 48202, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol301779e

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3. cFairweather, J. K.; Driguez, H.InCarbohydrates in Chemistry and Biology;Ernst, B.; Hart, G. W.; Sinay, P., Eds.Wiley-VCH:Weinheim, 2000; Vol.1, pp531–564.

4. Recent Advances in the Synthesis of Sialic Acid Derivatives and Sialylmimetics as Biological Probes

5. New ganglioside analogs that inhibit influenze virus sialidase

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