Pd-Catalyzed Enantio- and Regioselective Formation of Allylic Aryl Ethers
A general methodology for the synthesis of enantioenriched tertiary allylic aryl ethers through Pd-catalyzed decarbox- ylative reactions of vinyl cyclic carbonates and phenols is presented. Switching of the regioselectivity toward the formation of linear products by a judicious choice of the ligand...
| Autores: | , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2017 |
| 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:2072/356270 |
| Acceso en línea: | http://hdl.handle.net/2072/356270 https://doi.org/10.1021/acs.orglett.7b03247 |
| Access Level: | acceso abierto |
| Palabra clave: | 54 |
| Sumario: | A general methodology for the synthesis of enantioenriched tertiary allylic aryl ethers through Pd-catalyzed decarbox- ylative reactions of vinyl cyclic carbonates and phenols is presented. Switching of the regioselectivity toward the formation of linear products by a judicious choice of the ligand is also reported |
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