dc.contributor.author | Gevorgyan, Ashot | |
dc.contributor.author | Hopmann, Kathrin Helen | |
dc.contributor.author | Bayer, Annette | |
dc.date.accessioned | 2020-06-24T10:37:31Z | |
dc.date.available | 2020-06-24T10:37:31Z | |
dc.date.issued | 2020-01-31 | |
dc.description.abstract | A formal C−H carboxylation of unactivated arenes using CO<sub>2</sub> in green solvents is described. The present strategy combines a sterically controlled Ir‐catalyzed C−H borylation followed by a Cu‐catalyzed carboxylation of the in situ generated organoboronates. The reaction is highly regioselective for the C−H carboxylation of 1,3‐disubstituted and 1,2,3‐trisubstituted benzenes, 1,2‐ or 1,4‐symmetrically substituted benzenes, fluorinated benzenes and different heterocycles. The developed methodology was applied to the late‐stage C−H carboxylation of commercial drugs and ligands. | en_US |
dc.identifier.citation | Gevorgyan A, Hopmann KH, Bayer A. Formal C-H carboxylation of unactivated arenes with carbon dioxide. Chemistry - A European Journal. 2020 | en_US |
dc.identifier.cristinID | FRIDAID 1788743 | |
dc.identifier.doi | 10.1002/chem.202000515 | |
dc.identifier.issn | 0947-6539 | |
dc.identifier.issn | 1521-3765 | |
dc.identifier.uri | https://hdl.handle.net/10037/18646 | |
dc.language.iso | eng | en_US |
dc.publisher | European Chemical Societies Publishing | en_US |
dc.relation.journal | Chemistry - A European Journal | |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2020 The Author(s) | en_US |
dc.subject | VDP::Mathematics and natural science: 400::Chemistry: 440 | en_US |
dc.subject | VDP::Matematikk og Naturvitenskap: 400::Kjemi: 440 | en_US |
dc.title | Formal C-H carboxylation of unactivated arenes with carbon dioxide | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |