The Co(III)-catalyzed direct C–H amidation of arenes has been developed using O -acylcarbamates as a convenient amino source. This reaction proceeded in high efficiency under external oxidant-free conditions with a broad range of arene substrates, including 6-arylpurines bearing sensitive functional groups, thus furnishing synthetically versatile arene N -carbamate products.
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Patel et al. (2014) studied this question.
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