Rapid Synthesis of l -Idosyl Glycosyl Donors from α-Thioglucosides for the Preparation of Heparin Disaccharides-Reference-Cited by-同舟云学术

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Rapid Synthesis of l -Idosyl Glycosyl Donors from α-Thioglucosides for the Preparation of Heparin Disaccharides

Published:2018-06-28 Issue:25 Volume:2018 Page:3312-3316
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Herczeg Mihály¹^ORCID,Demeter Fruzsina¹,Balogh Tímea¹,Kelemen Viktor¹,Borbás Anikó¹^ORCID

Affiliation:

1. Department of Pharmaceutical Chemistry; University of Debrecen; Egyetem tér 1 H-4032 Debrecen Hungary

Funder

European Regional Development Fund

Mizutani Foundation for Glycoscience

National Research, Development and Innovation Office of Hungary

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference61 articles.

1. Structure and biological interactions of heparin and heparan sulfate

2. The Structure of Glycosaminoglycans and their Interactions with Proteins

3. Synthesis and Anticoagulant Activity of Bioisosteric Sulfonic-Acid Analogues of the Antithrombin-Binding Pentasaccharide Domain of Heparin

4. First Gram-Scale Synthesis of a Heparin-Related Dodecasaccharide

5. Synthesis of the Heparin-Based Anticoagulant Drug Fondaparinux

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3. Synthesis of the Three Most Expensive l-Hexose Thioglycosides from d-Glucose;Synthesis;2022-12-21

4. Synthesis of a Heparinoid Pentasaccharide Containing l-Guluronic Acid Instead of l-Iduronic Acid with Preserved Anticoagulant Activity;The Journal of Organic Chemistry;2022-11-21

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