Synthesis of Benzofuroquinolines via Phosphine-Free Direct Arylation of 4-Phenoxyquinolines in Air
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim A palladium-catalysed, phosphine-free, direct arylation of 4-phenoxyquinolines, in air is described. Using an intramolecular approach, the ring-closed products are formed in yields of up to 95 %. This approach allows access to a range of benzof...
| Main Authors: | , , , , |
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| Format: | Journal Article |
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Wiley-VCH Verlag GMBH
2018
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| Online Access: | http://hdl.handle.net/20.500.11937/72977 |
| _version_ | 1848762891151343616 |
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| author | Shanahan, R. Hickey, A. Reen, F. O'Gara, Fergal McGlacken, G. |
| author_facet | Shanahan, R. Hickey, A. Reen, F. O'Gara, Fergal McGlacken, G. |
| author_sort | Shanahan, R. |
| building | Curtin Institutional Repository |
| collection | Online Access |
| description | © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim A palladium-catalysed, phosphine-free, direct arylation of 4-phenoxyquinolines, in air is described. Using an intramolecular approach, the ring-closed products are formed in yields of up to 95 %. This approach allows access to a range of benzofuroquinolines. An array of functional groups on both the quinoline and phenoxy rings are tolerated. |
| first_indexed | 2025-11-14T10:54:46Z |
| format | Journal Article |
| id | curtin-20.500.11937-72977 |
| institution | Curtin University Malaysia |
| institution_category | Local University |
| last_indexed | 2025-11-14T10:54:46Z |
| publishDate | 2018 |
| publisher | Wiley-VCH Verlag GMBH |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | curtin-20.500.11937-729772018-12-13T09:34:00Z Synthesis of Benzofuroquinolines via Phosphine-Free Direct Arylation of 4-Phenoxyquinolines in Air Shanahan, R. Hickey, A. Reen, F. O'Gara, Fergal McGlacken, G. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim A palladium-catalysed, phosphine-free, direct arylation of 4-phenoxyquinolines, in air is described. Using an intramolecular approach, the ring-closed products are formed in yields of up to 95 %. This approach allows access to a range of benzofuroquinolines. An array of functional groups on both the quinoline and phenoxy rings are tolerated. 2018 Journal Article http://hdl.handle.net/20.500.11937/72977 10.1002/ejoc.201800923 Wiley-VCH Verlag GMBH restricted |
| spellingShingle | Shanahan, R. Hickey, A. Reen, F. O'Gara, Fergal McGlacken, G. Synthesis of Benzofuroquinolines via Phosphine-Free Direct Arylation of 4-Phenoxyquinolines in Air |
| title | Synthesis of Benzofuroquinolines via Phosphine-Free Direct Arylation of 4-Phenoxyquinolines in Air |
| title_full | Synthesis of Benzofuroquinolines via Phosphine-Free Direct Arylation of 4-Phenoxyquinolines in Air |
| title_fullStr | Synthesis of Benzofuroquinolines via Phosphine-Free Direct Arylation of 4-Phenoxyquinolines in Air |
| title_full_unstemmed | Synthesis of Benzofuroquinolines via Phosphine-Free Direct Arylation of 4-Phenoxyquinolines in Air |
| title_short | Synthesis of Benzofuroquinolines via Phosphine-Free Direct Arylation of 4-Phenoxyquinolines in Air |
| title_sort | synthesis of benzofuroquinolines via phosphine-free direct arylation of 4-phenoxyquinolines in air |
| url | http://hdl.handle.net/20.500.11937/72977 |