Synthesis of 3-Deoxy-α-d-manno-oct-2-ulosonic Acid Glycoside (Kdo) and Its 2-Deoxy Analogue: A Horner−Emmons Approach-Reference-Cited by-同舟云学术

Synthesis of 3-Deoxy-α-d-manno-oct-2-ulosonic Acid Glycoside (Kdo) and Its 2-Deoxy Analogue: A Horner−Emmons Approach

Published:1999-11-02 Issue:11 Volume:1 Page:1709-1711
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Młynarski Jacek¹,Banaszek Anna¹

Affiliation:

1. Institute of Organic Chemistry, Polish Academy of Sciences, 01-224 Warsaw, Poland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol990931j

Reference44 articles.

1. The Chemistry and Biological Significance of 3-Deoxy-d-manno-2-Octulosonic Acid (KDO)

2. Holst, O.; Brade, H. InBacterial Endotoxic Lipopolysaccharides; Morrison, D. C., Ryan, J. L., Eds.; CRC Press: Boca Raton, FL, 1992; Vol. 1, p 135.

3. 3-deoxy-d-manno-2-octulosonic acid (KDO) is a component of rhamnogalacturonan II, a pectic polysaccharide in the primary cell walls of plants

4. Total synthesis of (.+-.)-3-deoxy-D-manno-2-octulopyranosate

5. A new synthesis of 3-deoxy-d--2-octulosonic acid (kdo) from d-mannose

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