The Sialic Acids Waltz: Novel Stereoselective Isomerization of the 1,7-Lactones ofN-Acetylneuraminic Acids into the Corresponding γ-Lactones and Back to the Free Sialic Acids-Reference-Cited by-同舟云学术

The Sialic Acids Waltz: Novel Stereoselective Isomerization of the 1,7-Lactones ofN-Acetylneuraminic Acids into the Corresponding γ-Lactones and Back to the Free Sialic Acids

Published:2015-10-06 Issue:11 Volume:4 Page:1315-1321
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Rota Paola¹²^ORCID,Allevi Pietro²^ORCID,Anastasia Luigi³¹^ORCID

Affiliation:

1. Laboratory of Stem Cells for Tissue Engineering; IRCCS Policlinico San Donato; San Donato 20097 Milan Italy

2. Department of Biomedical, Surgical and Dental Sciences; University of Milan; Via Saldini 50 20133 Milan Italy

3. Department of Biomedical Sciences for Health; University of Milan; Segrate 20090 Milan Italy

Publisher

Wiley

Subject

Organic Chemistry

Reference35 articles.

1. Chemical Diversity in the Sialic Acids and Related α-Keto Acids: An Evolutionary Perspective

2. Advances in the Biology and Chemistry of Sialic Acids

3. Diversity of sialic acids revealed using gas chromatography/mass spectrometry of heptafluorobutyrate derivatives

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

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