The author of 《Gold redox catalysis for cyclization/arylation of allylic oximes: synthesis of isoxazoline derivatives》 were Jimoh, Abiola Azeez; Hosseyni, Seyedmorteza; Ye, Xiaohan; Wojtas, Lukasz; Hu, Yong; Shi, Xiaodong. And the article was published in Chemical Communications (Cambridge, United Kingdom) in 2019. Recommanded Product: 4-Iodobenzaldehyde The author mentioned the following in the article:
Base-assisted diazonium activation has been employed to promote gold(I)/(III) redox catalysis toward allylic oxime cyclization/aryl coupling. Isoxazolines I (R1 = cyclohexyl, Ph, 3-MeC6H4, 2-naphthyl, etc.; R2 = 4-FC6H4, 4-MeO2CC6H4, 3-EtO-4-F3CC6H3, etc.) were prepared in good to excellent yields from allylic oximes II and aryldiazonium salts R2N2+BF4- using this method, whereas the alternative photoactivation method provided only trace amounts of the isoxazoline products. This study further broadens the scope of gold redox chem. The results came from multiple reactions, including the reaction of 4-Iodobenzaldehyde(cas: 15164-44-0Recommanded Product: 4-Iodobenzaldehyde)
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: 4-Iodobenzaldehyde
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com