| Autor: |
Weires NA; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, USA., Baker EL; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, USA., Garg NK; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, USA. |
| Abstrakt: |
The Suzuki-Miyaura coupling has become one of the most important and prevalent methods for the construction of C-C bonds. Although palladium catalysis has historically dominated the field, the use of nickel catalysis has become increasingly widespread because of its unique ability to cleave carbon-heteroatom bonds that are unreactive towards other transition metals. We report the first nickel-catalysed Suzuki-Miyaura coupling of amides, which proceeds by an uncommon cleavage of the amide C-N bond after N-tert-butoxycarbonyl activation. The methodology is mild, functional-group tolerant and can be strategically employed in sequential transition-metal-catalysed cross-coupling sequences to unite heterocyclic fragments. These studies demonstrate that amides, despite classically considered inert substrates, can be harnessed as synthons for use in reactions that form C-C bonds through cleavage of the C-N bond using non-precious metal catalysis. |
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