“…As shown in Scheme 3, a wide range of electron-deficient alkenes containing aromatic moieties with varied electronic and steric properties (4- MeOC 6 H 4 , 4-MeC 6 H 4 , 4-t BuC 6 H 4 , 4-OHC 6 H 4 , 4-PhC 6 H 4 , 4-FC 6 H 4 , 4-BrC 6 H 4 , 4-CF 3 C 6 H 4 , 2-MeC 6 H 4 , 2,4-diMeC 6 H 3 ) were well tolerated in this protocol, and the corres- ponding addition products 3a-3x could be delivered in moderate to excellent yields (55-93%) under standard conditions. Similarly, the heterocyclic furyl-based alkene that formed between commercially available furfural 18 and malononitrile proceeded smoothly in this reaction, leading to the desired product 3s with an important furan function retained in 55% yield. On the other hand, a variety of aniline derivatives uniformly underwent C(sp 3 )-H activation and subsequent aminoalkyl conjugate addition, producing γ-amino nitriles with complete selectivity.…”