Highly Efficient and Stereoselective Synthesis of 6,7‐Dideoxy‐β‐ d‐ ido ‐octopyranuronates
Author:
Affiliation:
1. Department of Chemistry University of Calgary 2500 University Drive NW Calgary AB T2N 1N4 Canada
Funder
University of Calgary
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202200175
Reference50 articles.
1. Conformation of Some Anomeric O-BenzylatedD-gluco-,L-Ido-, and Hex-4-enopyranoside derivatives
2. Dependence of Pyranose Ring Puckering on Anomeric Configuration: Methyl Idopyranosides
3. 1,3-syn-Diaxial Repulsion of Typical Protecting Groups Used in Carbohydrate Chemistry in 3-O-Substituted Derivatives of Isopropyl d-Idopyranosides
4. An investigation of the pyranose ring interconversion path of α-l-idose calculated using density functional theory
5. The Structure of Glycosaminoglycans and their Interactions with Proteins
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