75491-29-1Relevant 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.
Improved dimethylsulfoxonium methylide cyclopropanation procedures, including a tandem oxidation variant
Paxton, Richard J.,Taylor, Richard J. K.
, p. 633 - 637 (2007/10/03)
A new procedure for the cyclopropanation of α,β-unsaturated carbonyl compounds and related systems is described which employs trimethylsulfoxonium iodide and an organic base in acetonitile to generate dimethylsulfoxonium methylide in situ; in addition, pr
