O-Sialylation with N-Acetyl-5-N,4-O-Carbonyl-Protected Thiosialoside Donors in Dichloromethane: Facile and Selective Cleavage of the Oxazolidinone Ring-Reference-Cited by-同舟云学术

O-Sialylation with N-Acetyl-5-N,4-O-Carbonyl-Protected Thiosialoside Donors in Dichloromethane: Facile and Selective Cleavage of the Oxazolidinone Ring

Published:2007-03-01 Issue:7 Volume:72 Page:2387-2391
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Crich David¹,Li Wenju¹

Affiliation:

1. Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607-7061

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo062431r

Reference73 articles.

1. Sialic Acids

2. (b)Sialobiology and Other NovelForms of Glycosylation; Inoue, Y., Lee, Y. C., Troy, F. A., II, Eds.; Gakushin: Osaka, Japan, 1999.

3. Polyvalent Interactions in Biological Systems: Implications for Design and Use of Multivalent Ligands and Inhibitors

4. Selectin−Carbohydrate Interactions: From Natural Ligands to Designed Mimics

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