Total Synthesis of the Antidiabetic (Type 2) Lipid Mediator Protectin DX/PDX-Reference-Cited by-同舟云学术

Total Synthesis of the Antidiabetic (Type 2) Lipid Mediator Protectin DX/PDX

Published:2018-12-26 Issue:2 Volume:84 Page:495-505
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Sancéau Jean-Yves¹^ORCID,Maltais René¹^ORCID,Poirier Donald¹²^ORCID,Marette André³

Affiliation:

1. Organic Synthesis Service, Medicinal Chemistry Platform, Centre Hospitalier Universitaire (CHU) de Québec-Research Center, Québec, QC, G1V 4G2, Canada

2. Department of Molecular Medicine, Faculty of Medicine, Université Laval, Québec, QC, G1V 0A6, Canada

3. Department of Medicine, Québec Heart and Lung Institute, Laval Hospital, Québec, QC G1V 4G5, Canada

Funder

Canadian Institutes of Health Research

Pfizer

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b01973

Reference46 articles.

1. Does promoting resolution instead of inhibiting inflammation represent the new paradigm in treating infections?

2. Bioactive metabolites of docosahexaenoic acid

3. DHA- and EPA-derived resolvins, protectins, and maresins in airway inflammation

4. Pro-resolving lipid mediators are leads for resolution physiology

5. Resolvins, Specialized Proresolving Lipid Mediators, and Their Potential Roles in Metabolic Diseases

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1. Biotransformation of docosahexaenoic acid into 10R,17S-dihydroxydocosahexaenoic acid as protectin DX 10-epimer by serial reactions of arachidonate 8R- and 15S-lipoxygenases;World Journal of Microbiology and Biotechnology;2024-05-29

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3. Organochromium Reagents;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2024

4. Biotransformation of docosahexaenoic acid into 10R,17S- dihydroxydocosahexaenoic acid as protectin Dx 10-epimer by serial reactions of arachidonate 8R- and 15S-lipoxygenases;2023-11-16

5. A Concise, Gram-Scale Total Synthesis of Protectin DX and Related Labeled Versions via a Key Stereoselective Reduction of Enediyne;The Journal of Organic Chemistry;2023-05-12