Stereoselective Synthesis of α(2,9) Di- to Tetrasialic Acids, Using a 5,4-N,O-Carbonyl Protected Thiosialoside-Reference-Cited by-同舟云学术

Stereoselective Synthesis of α(2,9) Di- to Tetrasialic Acids, Using a 5,4-N,O-Carbonyl Protected Thiosialoside

Published:2009-05-04 Issue:11 Volume:74 Page:4383-4386
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Tanaka Hiroshi¹,Nishiura Yuji¹,Takahashi Takashi¹

Affiliation:

1. Department of Applied Chemistry, Graduate School of Science and Engineering, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro, Tokyo 152-8552, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo900176e

Reference38 articles.

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2. Glycobiology of Di- and Oligosialyl Glycotopes.

3. Embryonal lactosaminoglycan. The structure of branched lactosaminoglycans with novel disialosyl (sialyl alpha 2—-9 sialyl) terminals isolated from PA1 human embryonal carcinoma cells.

4. Discovery of an α2,9-PolyNeu5Ac Glycoprotein in C-1300 Murine Neuroblastoma (Clone NB41A3)

5. Flagellasialin: a novel sulfated 2,9-linked polysialic acid glycoprotein of sea urchin sperm flagella

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