Visible-Light-Promoted C(sp3)–H Bond Functionalization toward Aminothiazole Skeletons from Active Methylene Ketones and Thioureas
Author:
Affiliation:
1. School of Pharmaceutical and Chemical Engineering, Taizhou University
2. Advanced Research Institute and School of Pharmaceutical Sciences, Taizhou University
3. Department of Chemistry, Zhejiang Sci-Tech University
Abstract
Funder
Natural Science Foundation of Zhejiang Province
National Natural Science Foundation of China
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry,Catalysis
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/a-2035-2873.pdf
Reference46 articles.
1. Structure–activity relationships of 2-aminothiazoles effective against Mycobacterium tuberculosis
2. 2-Aminothiazole derivatives as antimycobacterial agents: Synthesis, characterization, in vitro and in silico studies
3. Discovery of 4-Aryl-N-arylcarbonyl-2-aminothiazoles as Hec1/Nek2 Inhibitors. Part I: Optimization of in Vitro Potencies and Pharmacokinetic Properties
4. Design, synthesis, and biological evaluation of aminothiazole derivatives against the fungal pathogens Histoplasma capsulatum and Cryptococcus neoformans
5. 2-Aminothiazole-Derived Opioids. Bioisosteric Replacement of Phenols
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1. Recent Progress in the Synthesis of Thiazole-Containing Compounds;Chinese Journal of Organic Chemistry;2024
2. TsNBr2 promoted cascade formation of C–N and C–S bond: Metal-free synthesis of 2-aminothiazoles from ketones or ketoximes using thiourea;Tetrahedron;2023-12
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