Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines
A general synthetic route to prepare all four carboline regioisomers by photostimulated cyclization of anilinohalopyridines is described. The methodology affords various substituted carbolines in good to excellent yields. In the case of α-carbolines, the S(RN)1 methodology complements previously rep...
| Autores: | , , , |
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| Formato: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2011 |
| País: | Argentina |
| Recursos: | Consejo Nacional de Investigaciones Científicas y Técnicas |
| Repositorio: | CONICET Digital (CONICET) |
| Idioma: | inglés |
| OAI Identifier: | oai:ri.conicet.gov.ar:11336/66183 |
| Acesso em linha: | http://hdl.handle.net/11336/66183 |
| Access Level: | acceso abierto |
| Palavra-chave: | Srn1 Carbolines Photochemistry Ring Closure https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| Resumo: | A general synthetic route to prepare all four carboline regioisomers by photostimulated cyclization of anilinohalopyridines is described. The methodology affords various substituted carbolines in good to excellent yields. In the case of α-carbolines, the S(RN)1 methodology complements previously reported palladium-catalyzed cyclization approaches. |
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