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In the manuscript, Table 3 described the coupling of heteroaryl derived oximes with alkynes. We depicted the coupling of a pyridyl-derived oxime as delivering the bicyclic adduct 5h with an attendant statement that ‘‘the C H activation occurs predominately at the position adjacent to the nitrogen.’’ The ESI had the wrong H and C NMR spectra for 5h. We have reinvestigated the reaction and find that it affords a 4 : 1 ratio of 5h to the regioisomeric adduct 5h0. Clearly, the predominant mode of reactivity is at the 4-postion of the pyridine. The appropriate H and C NMR spectra have been replaced in the ESI.

Correction: Pyridine synthesis from oximes and alkynes via rhodium(iii) catalysis: Cp* and Cpt provide complementary selectivity

Correction: Pyridine synthesis from oximes and alkynes via rhodium(iii) catalysis: Cp* and Cp^t provide complementary selectivity