An Efficient Route toward 2-Amino-β-d-galacto- and -glucopyranosides via Stereoselective Michael-Type Addition of 2-Nitroglycals-Reference-Cited by-同舟云学术

An Efficient Route toward 2-Amino-β-d-galacto- and -glucopyranosides via Stereoselective Michael-Type Addition of 2-Nitroglycals

Published:2009-05-19 Issue:14 Volume:74 Page:5079-5082
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Xue Weihua¹,Sun Jiansong¹,Yu Biao¹

Affiliation:

1. State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo900609s

Reference29 articles.

1. Chemistry, Metabolism, and Biological Functions of Sialic Acids

2. Tumor-Associated Carbohydrate Antigens

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4. The Emerging Significance of O-GlcNAc in Cellular Regulation

5. Results and Problems ofO-Glycoside Synthesis

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