Affiliation:
1. Faculty of Sciences, Department of Chemistry, Atatürk University, Erzurum 25240, Turkey
Abstract
We report a highly site-selective direct C5–H and N–H alkylation of free amine group-bearing 8-aminoquinolines in high to excellent yields.
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis
Cited by
9 articles.
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1. 1,1,1,3,3,3-Hexafluoro-2-propanol (HFIP)-promoted regiospecific 1,6-hydroarylation of para-quinone methides with N-heteroarenes: Synthesis of unsymmetrical triarylmethanes;Tetrahedron;2024-05
2. Ruthenium-Catalyzed 1,6-Hydroalkylation of para-Quinone Methides with Ketones via the in Situ Activation of C(sp3)–H Bonds;The Journal of Organic Chemistry;2023-11-13
3. Catalyst‐ and Additive‐free, Regioselective 1,6‐Hydroarylation of para‐Quinone Methides with Anilines in HFIP;Chemistry – An Asian Journal;2023-11-02
4. Acetic Acid‐Catalyzed 1,6‐Addition of Indolizine to para‐Quinone Methides;Asian Journal of Organic Chemistry;2023-06-12
5. Six-membered ring systems: pyridines and benzo derivatives;Progress in Heterocyclic Chemistry;2023