42205-91-4Relevant academic research and scientific papers
Visible-light-induced triple catalysis for a ring-opening cyanation of cyclopropyl ketones
Liu, Jing,Liu, Xiao-Peng,Wu, Hong,Wei, Yi,Lu, Fu-Dong,Guo, Kai-Rui,Cheng, Ying,Xiao, Wen-Jing
supporting information, p. 11508 - 11511 (2020/10/12)
An unprecedented triple catalytic, general ring-opening cyanation reaction of cyclopropyl ketones for the construction of γ-cyanoketones is described. The key is to merge photoredox catalysis with Lewis acid catalysis and copper catalysis to enable the selective cleavage of the carbon-carbon bonds and the selective coupling of the generated radical and cyanide anion.
Palladium-catalyzed cross-coupling of styrenes with aryl methyl ketones in ionic liquids: Direct access to cyclopropanes
Cotugno, Pietro,Monopoli, Antonio,Ciminale, Francesco,Milella, Antonella,Nacci, Angelo
supporting information, p. 13563 - 13567 (2015/01/09)
The combined use of Pd(OAc)2, Cu(OAc)2, and dioxygen in molten tetrabutylammonium acetate (TBAA) promotes an unusual cyclopropanation reaction between aryl methyl ketones and styrenes. The process is a dehydrogenative cyclizing coupl
