2,3-Diodocarbazoles by a Domino Iodocyclization/Iodo-Translocation of (3-Iodoindolyl)butynols
A controlled access to 1-aryl 2,3-diiodo-carbazoles involving iodine transposition has been accomplished directly from acyclic precursors. The 2,3-diiodo-carbazole core was prone to further chemoselective decoration at C3−I or double difunctionalization. (Figure presented.).
| Autores: | , , , , |
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| Tipo de documento: | artigo |
| Estado: | Versão publicada |
| Data de publicação: | 2022 |
| País: | España |
| Recursos: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositório: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/288902 |
| Acesso em linha: | http://hdl.handle.net/10261/288902 |
| Access Level: | Acceso aberto |
| Palavra-chave: | carbazole cascade reactions cyclization iodine translocation Metal-free |
| Resumo: | A controlled access to 1-aryl 2,3-diiodo-carbazoles involving iodine transposition has been accomplished directly from acyclic precursors. The 2,3-diiodo-carbazole core was prone to further chemoselective decoration at C3−I or double difunctionalization. (Figure presented.). |
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