Stereoselective Synthesis of 2-C-Branched (Acetylmethyl) Oligosaccharides and Glycoconjugates: Lewis Acid-Catalyzed Glycosylation from 1,2-Cyclopropaneacetylated Sugars-Reference-Cited by-同舟云学术

Stereoselective Synthesis of 2-C-Branched (Acetylmethyl) Oligosaccharides and Glycoconjugates: Lewis Acid-Catalyzed Glycosylation from 1,2-Cyclopropaneacetylated Sugars

Published:2011-01-19 Issue:4 Volume:76 Page:1045-1053
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Tian Qiang¹,Dong Liang²,Ma Xiaofeng¹,Xu Liyan¹,Hu Changwei²,Zou Wei³,Shao Huawu¹

Affiliation:

1. Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, China

2. Key Laboratory of Green Chemistry and Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China

3. Institute for Biological Sciences, National Research Council of Canada, 100 Sussex Drive, Ottawa, Ontario K1A 0R6, Canada, and Graduate School of Chinese Academy of Sciences, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo1016579

Reference53 articles.

1. Ketone Isosteres of 2-N-Acetamidosugars as Substrates for Metabolic Cell Surface Engineering

2. Exploiting Differences in Sialoside Expression for Selective Targeting of MRI Contrast Reagents

3. Metabolic Delivery of Ketone Groups to Sialic Acid Residues

4. Engineering Novel Cell Surface Receptors for Virus-mediated Gene Transfer

5. Novel Method for in Vitro O-Glycosylation of Proteins: Application for Bioconjugation

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