. 2016 Oct 27;6(12):8004–8008. doi: 10.1021/acscatal.6b02786

Table 1. Optimization of the Reaction Conditions^a.

graphic file with name cs-2016-02786y_0005.jpg

graphic file with name cs-2016-02786y_0006.jpg

2a (0.1 mmol), 1a (0.12 mmol), 4CzIPN (3 mol %), [Ni(dtbbpy)(H₂O)₄]Cl₂ (5 mol %) in dry, degassed solvent (2.0 mL, 0.05 M) under blue LED irradiation for 24 h. ^bHPLC yield using 4,4′-di-tert-butylbiphenyl as an internal standard. ^cIsolated yield.

Table 1. Optimization of the Reaction Conditionsa.

Table 1. Optimization of the Reaction Conditions^a.