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.).
| Authors: | , , , , |
|---|---|
| Format: | article |
| Status: | Published version |
| Publication Date: | 2022 |
| Country: | España |
| Institution: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repository: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/288902 |
| Online Access: | http://hdl.handle.net/10261/288902 |
| Access Level: | Open access |
| Keyword: | carbazole cascade reactions cyclization iodine translocation Metal-free |
| Summary: | 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.). |
|---|