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Formal C-H carboxylation of unactivated arenes with carbon dioxide

Permanent link
https://hdl.handle.net/10037/18646
DOI
https://doi.org/10.1002/chem.202000515
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Date
2020-01-31
Type
Journal article
Tidsskriftartikkel
Peer reviewed

Author
Gevorgyan, Ashot; Hopmann, Kathrin Helen; Bayer, Annette
Abstract
A formal C−H carboxylation of unactivated arenes using CO2 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.
Publisher
European Chemical Societies Publishing
Citation
Gevorgyan A, Hopmann KH, Bayer A. Formal C-H carboxylation of unactivated arenes with carbon dioxide. Chemistry - A European Journal. 2020
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