The front cover picture, provided by Takahiko Akiyama and co-workers, illustrates a concise route to 3-aryl-1-trifluoromethyltetrahydroisoquinolines by benzylic [1,5-hydride shift mediated CH bond functionalization. The [1,5]-hydride shift of the benzylic C(sp3)H bond to trifluoromethyl ketimine occurred smoothly to produce the target skeleton in good to excellent chemical yields. Whereas N-4-methoxyphenyl ketimines gave the cis-isomer predominantly, use of NH ketimines changed the diastereoselectivity to furnish the trans-isomer stereoselectively. Details can be found in the communication on pages 901–906 (K. Mori, N. Umehara, T. Akiyama, Adv. Synth. Catal. 2015, 357, 901–906; DOI: 10.1002/adsc.201400775).