Abstract
An efficient o-arylation of pivalamides by aryl iodides via rhodium(III)-catalyzed C-H activation is demonstrated for the first time. Further, the biaryl products can be converted effectively into biologically active phenanthridine and phenanthridinone derivative.
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Haridharan, R., Muralirajan, K., & Cheng, C. H. (2015). Rhodium(III)-catalyzed ortho-arylation of anilides with aryl halides. Advanced Synthesis and Catalysis, 357(2–3), 366–370. https://doi.org/10.1002/adsc.201400798
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