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Issue 17, 2013
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Direct acylation of N-benzyltriflamides from the alcohol oxidation level via palladium-catalyzed C–H bond activation

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Abstract

A palladium-catalyzed ortho-acylation of N-benzyltriflamides from the alcohol oxidation level via C–H bond activation is described. These transformations have been applied to a wide range of substrates, and typically proceed with excellent levels of chemoselectivity and with high functional group tolerance.

Graphical abstract: Direct acylation of N-benzyltriflamides from the alcohol oxidation level via palladium-catalyzed C–H bond activation

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Publication details

The article was received on 22 Jan 2013, accepted on 26 Feb 2013 and first published on 26 Feb 2013


Article type: Paper
DOI: 10.1039/C3OB40140E
Citation: Org. Biomol. Chem., 2013,11, 2766-2771
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    Direct acylation of N-benzyltriflamides from the alcohol oxidation level via palladium-catalyzed C–H bond activation

    J. Park, A. Kim, S. Sharma, M. Kim, E. Park, Y. Jeon, Y. Lee, J. H. Kwak, Y. H. Jung and I. S. Kim, Org. Biomol. Chem., 2013, 11, 2766
    DOI: 10.1039/C3OB40140E

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