Halogenating agent-promoted transformation of enaminones into α,α-dihaloketones (halo = Cl, Br)
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. Recent advances in transition metal-free annulation toward heterocycle diversity based on the C–N bond cleavage of enaminone platform
2. Tunable Key [3 + 2] and [2 + 1] Cycloaddition of Enaminones and α-Diazo Compounds for the Synthesis of Isomeric Isoxazoles: Metal-Controlled Selectivity
3. Amine-catalyzed synthesis of N2-sulfonyl 1,2,3-triazole in water and the tunable N2-H 1,2,3-triazole synthesis in DMSO via metal-free enamine annulation
4. Cascade in Situ Iodination, Chromone Annulation, and Cyanation for Site-Selective Synthesis of 2-Cyanochromones
5. Highly Site-Selective Metal-Free C–H Acyloxylation of Stable Enamines
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2. Oxidative Free-Radical C(sp2)–H Bond Chlorination of Enaminones with LiCl: Access to Highly Functionalized α-Chlorinated Enaminones;The Journal of Organic Chemistry;2024-06-03
3. Catalyst-free reactions of anilines with β-chloroenones: synthesis of α-chloroenaminones and 1,4-benzodiazepines;Organic & Biomolecular Chemistry;2024
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