Development of a new approach for the synthesis of (+)-15-deoxy-Δ12,14-prostaglandin J2 methyl ester based on the [2+2]-cycloadduct of 5-trimethylsilylcyclopentadiene and dichloroketene
Author:
Affiliation:
1. Ufa Institute of Chemistry (UfIC), Ufa Federal Research Centre of the Russian Academy of Sciences (UFIC RAS) Pr. Oktyabrya, 71, Ufa, 450054, Russian Federation
Abstract
Funder
Federal Agency for Scientific Organizations
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ01003H
Reference60 articles.
1. The eicosanoids and their biochemical mechanisms of action
2. Albumin-catalyzed metabolism of prostaglandin D2. Identification of products formed in vitro.
3. 9-Deoxy-delta 9, delta 12-13,14-dihydroprostaglandin D2, a metabolite of prostaglandin D2 formed in human plasma.
4. Regulation of Nrf2-dependent gene expression by 15-deoxy-Δ12,14-prostaglandin J2
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1. Synthesis of (S)-N-Ethyl-2-(5-methylidene-4-oxocyclopent-2-en-1-yl)acetamide―A Model exo-Methylidenecyclopentenone Bioisoster of Prostamides;Russian Journal of Organic Chemistry;2024-02
2. Some aspects of the synthesis and modification of cross-conjugated cyclopentenone prostaglandins;Russian Chemical Bulletin;2023-10
3. A facile synthesis of (±)-15-deoxy-Δ12,14-prostaglandin J2 methyl ester;Mendeleev Communications;2023-07
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