1380341-59-2Relevant academic research and scientific papers
Carbocation catalysed ring closing aldehyde-olefin metathesis
Ni, Shengjun,Franzén, Johan
supporting information, p. 12982 - 12985 (2018/11/23)
A highly efficient aldehyde-olefin metathesis catalysed by the carbocation, 4-phenylphenyl-diphenylmethylium ion, has been developed. This protocol is characterized by high yields, low catalyst loading (down to 2 mol%), good functional group compatibility and mild reaction conditions.
Nickel-catalyzed heck-type alkenylation of secondary and tertiary α-carbonyl alkyl bromides
Liu, Chao,Tang, Shan,Liu, Dong,Yuan, Jiwen,Zheng, Liwei,Meng, Lingkui,Lei, Aiwen
supporting information; experimental part, p. 3638 - 3641 (2012/05/20)
Ni made it! A novel Heck-type reaction of secondary and tertiary α-carbonyl alkyl bromides, most likely involving a radical process, was achieved through the use of a nickel catalyst. Various substituted styrenes and 1,1-diaryl alkenes were utilized as substrates to easily construct α-alkenyl carbonyl compounds with tertiary or quaternary carbon centers. A catalytic cycle involving NiI/NiII is proposed based on our experimental results. EWG=electron-withdrawing group.
