《NiH-catalyzed asymmetric hydroarylation of N-acyl enamines to chiral benzylamines》 was written by He, Yuli; Song, Huayue; Chen, Jian; Zhu, Shaolin. Application of 15164-44-0 And the article was included in Nature Communications in 2021. The article conveys some information:
NiH-catalyzed enantio- and regioselective reductive hydroarylation of N-acyl enamines, allowed for the practical access to a broad range of structurally diverse, enantioenriched benzylamines under mild, operationally simple reaction conditions was reported.4-Iodobenzaldehyde(cas: 15164-44-0Application of 15164-44-0) was used in this study.
4-Iodobenzaldehyde(cas: 15164-44-0) is used in synthesis of 4-[2-(trimethylsilyl)ethynyl]benzaldehyde, 5,15-dimesityl-10-(3-[2-(trimethylsilyl)ethynyi]phenyl}-20-(4-iodophenyl)porphyrin, and 5,15-dimesityl-10-[3,5-bis{2-[4-(N,N’-difluoroboryl-1,9-dimethyidipyrrin-5-yl)-phenyl]ethynyl}phenyl]-20-(4-iodophenyl)porphyrin.Application of 15164-44-0
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com