Photoredox-Assisted Gold-Catalyzed Arylative Alkoxycyclization of 1,6-Enynes
The photoredox-assisted gold-catalyzed arylative cyclization of 1,6-enynes with aryldiazonium salts gives rise to cyclization products with the opposite configuration at the alkene than that obtained by gold(I)-catalyzed alkoxycyclization. The reaction occurs under mild conditions and shows high fun...
| Autores: | , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2020 |
| 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:2072/447789 |
| Acceso en línea: | http://hdl.handle.net/2072/447789 https://doi.org/10.1021/acs.orglett.0c00799 |
| Access Level: | acceso abierto |
| Palabra clave: | 54 |
| Sumario: | The photoredox-assisted gold-catalyzed arylative cyclization of 1,6-enynes with aryldiazonium salts gives rise to cyclization products with the opposite configuration at the alkene than that obtained by gold(I)-catalyzed alkoxycyclization. The reaction occurs under mild conditions and shows high functional group tolerance. |
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