Iron-Catalyzed Intermolecular N-H Insertion Using Acceptor-Acceptor Carbenes Derived from Iodonium Ylides
In this study, we report a general and efficient method for the iron-catalyzed intermolecular N-H insertion at the intercarbonylic position of malonate reagents. Using iodonium ylides and simple iron(II) triflate as the catalyst, the reaction enables the func-tionalization of a wide range of primary...
| Autores: | , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2025 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:10256/27142 |
| Acceso en línea: | http://hdl.handle.net/10256/27142 |
| Access Level: | acceso abierto |
| Palabra clave: | Amines Carbens Catalitzadors Reaccions químiques Ferro Carbenes Catalysts Chemical reactions Iron |
| Sumario: | In this study, we report a general and efficient method for the iron-catalyzed intermolecular N-H insertion at the intercarbonylic position of malonate reagents. Using iodonium ylides and simple iron(II) triflate as the catalyst, the reaction enables the func-tionalization of a wide range of primary and secondary aromatic and aliphatic amines in excellent yields. The reaction operates under exceptionally mild conditions, without the need for an inert atmosphere or anhydrous solvents, and proceeds in remark-ably short reaction times. Mechanistic studies support a non-radical pathway in which an iron(II)-stabilized intermediate hav-ing hybrid carbene/carbocationic character undergoes nucleophilic attack by the amine |
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