A photo-induced α-C(sp)-H decyanative pyridination of -arylglycine derivatives with cyanopyridines was developed. This reaction was performed under organic photocatalytic and redox-neutral conditions a radical-radical cross-coupling process. Besides, the protocol was also suitable for the C(sp)-H pyridination of -aryl tetrahydroisoquinolines as well as benzylamines.

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http://dx.doi.org/10.1039/d4cc00906aDOI Listing

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