Why Is Direct Glycosylation with N-Acetylglucosamine Donors Such a Poor Reaction and What Can Be Done about It?
Author:
Affiliation:
1. Department of Chemistry, Aarhus University, Langelandsgade 140, 8000 Aarhus C, Denmark
Funder
Villum Fonden
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b02305
Reference34 articles.
1. Glycomics Hits the Big Time
2. Exploring the Structural Diversity of Mammalian Carbohydrates (“Glycospace”) by Statistical Databank Analysis
3. Stereoselective Glycosylation of Glucosamine: The Role of the N ‐Protecting Group
4. Recent trends in the synthesis of O-glycosides of 2-amino-2-deoxysugars
5. Why Are the Hydroxy Groups of Partially Protected N-Acetylglucosamine Derivatives Such Poor Glycosyl Acceptors, and What Can Be Done about It? A Comparative Study of the Reactivity of N-Acetyl-, N-Phthalimido-, and 2-Azido-2-deoxy-glucosamine Derivatives in Glycosylation. 2-Picolinyl Ethers as Reactivity-Enhancing Replacements for Benzyl Ethers
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