Yang, Liming; Xie, Henan; An, Guanghui; Li, Guangming published their research in Journal of Organic Chemistry in 2021. The article was titled 《Acid-Enabled Palladium-Catalyzed β-C(sp3)-H Functionalization of Weinreb Amides》.Recommanded Product: 15164-44-0 The article contains the following contents:
Herein, Pd(II)-catalyzed C(sp3)-H arylation and alkenylation of Weinreb amides was reported. A com. available, inexpensive sulfonic acid was employed to enhance the coordination of the catalyst with weak-coordinating substrates by increasing the electrophilicity of in situ formed palladium catalysts. The results came from multiple reactions, including the reaction of 4-Iodobenzaldehyde(cas: 15164-44-0Recommanded Product: 15164-44-0)
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.Recommanded Product: 15164-44-0
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com