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. 2018 Sep 12;9(44):8453–8460. doi: 10.1039/c8sc02965b

Table 2. Substrate scope for benzylic Csp3–H arylation of N-benzylamines a .

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aAll reactions were conducted on 1 mmol scale.

bTerephthalonitrile was used as an arylating reagent (Ar′ = 4-NCC6H4).

cThe reaction was carried out for 6 h.

dYield and regioisomeric ratio were determined by 1H NMR analysis using 1,1,2,2-tetrachloroethane as an internal standard.