The cover picture, provided by
Yuhong Zhang and co-workers, illustrates a highly efficient synthesis of pyrrolidones by the copper-catalyzed alkynylation/annulation of aliphatic amides with alkynyl carboxylic acids. A broad range of easily accessible alkynyl carboxylic acids was introduced at the β-methyl group of aliphatic amides with the assistance of an 8-aminoquinolyl auxiliary group
via decarboxylation to achieve the subsequent cyclic CN bond formation within one hour. This catalytic tandem decarboxylative cyclization provides a new opportunity for the direct functionalization of
sp3 CH bonds. Details can be found in the full paper on pages 792–807 (J. Zhang, D. Li, H. Chen, B.
Wang, Z. Liu, Y. Zhang,
Adv. Synth. Catal.
2016,
358, 792–807; DOI:
10.1002/adsc.201500727).