| Literature DB >> 27813308 |
Liana Hie1, Emma L Baker1, Sarah M Anthony1, Jean-Nicolas Desrosiers2, Chris Senanayake2, Neil K Garg1.
Abstract
Recent studies have demonstrated that amides can be used in nickel-catalyzed reactions that lead to cleavage of the amide C-N bond, with formation of a C-C or C-heteroatom bond. However, the general scope of these methodologies has been restricted to amides where the carbonyl is directly attached to an arene or heteroarene. We now report the nickel-catalyzed esterification of amides derived from aliphatic carboxylic acids. The transformation requires only a slight excess of the alcohol nucleophile and is tolerant of heterocycles, substrates with epimerizable stereocenters, and sterically congested coupling partners. Moreover, a series of amide competition experiments establish selectivity principles that will aid future synthetic design. These studies overcome a critical limitation of current Ni-catalyzed amide couplings and are expected to further stimulate the use of amides as synthetic building blocks in C-N bond cleavage processes.Entities:
Keywords: aliphatic amides; cross-coupling; esterification; homogeneous catalysis; nickel
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Year: 2016 PMID: 27813308 PMCID: PMC5161497 DOI: 10.1002/anie.201607856
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336