Synthesis of Anticoagulant Pentasaccharide Fondaparinux via 3,5-Dimethyl-4-(2′-phenylethynylphenyl)phenyl Glycosides-Reference-Cited by-同舟云学术

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Synthesis of Anticoagulant Pentasaccharide Fondaparinux via 3,5-Dimethyl-4-(2′-phenylethynylphenyl)phenyl Glycosides

Published:2023-11-20 Issue:47 Volume:25 Page:8506-8510
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liu Wei¹,Hu Zhifei¹,Xu Peng²³^ORCID,Yu Biao²³^ORCID

Affiliation:

1. School of Physical Science and Technology, ShanghaiTech University, 100 Haike Road, Shanghai 201210, China

2. State Key Laboratory of Chemical Biology, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China

3. School of Chemistry and Materials Science, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, 1 Sub-lane Xiangshan, Hangzhou 310024, China

Funder

Youth Innovation Promotion Association of the Chinese Academy of Sciences

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Chinese Academy of Sciences

Shanghai Municipal Science and Technology Major Project

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c03484

Reference49 articles.

1. Heparin and anticoagulation

2. Pharmacology of Heparin and Related Drugs

3. Novel drug development opportunities for heparin

4. Advances in the preparation and synthesis of heparin and related products

5. Structure of the antithrombin-binding site in heparin.

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1. Overview of the current procedures in synthesis of heparin saccharides;Carbohydrate Polymers;2024-09

2. Stereoselective α‐Glycosylation with GlcN₃ Donors Enabled Collective Syntheses of Acinetobacter baumannii Capsular Polysaccharides K43, K47 and K88 Repeating Units^†;Chinese Journal of Chemistry;2024-03-13

3. Synthesis of the Reducing‐end Hexasaccharide Fragment of Marine Lipopolysaccharide Axinelloside A;Chemistry – A European Journal;2024-01-22

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