Cover Picture: Palladium-Catalyzed Intermolecular Oxidative Coupling Reactions of (Z)-Enamines with Isocyanides through Selective β-C(sp2)-H and/or C=C Bond Cleavage (Chin. J. Chem. 8/2018)
Abstract
The cover picture shows Two efficient intermolecular oxidative coupling reactions of (Z)-enamines with isocyanides via palladium catalysis have been developed. In these transformations, the β-C(sp2)-H and/or C = C bond were cut off selectively by using different anionic ligands, leading to controllable chemodivergent and stereoselective construction of a wide range of (E)β-carbamoylenamine derivatives with intramolecular hydrogen bonds. More details are discussed in the article by Jiang et al. on page 712–715.