70671-92-0Relevant academic research and scientific papers
Acetoxylation and hydroxylation of diarylmethylenecycloalkanes via radical approach
Jiang, Min,Wei, Yin,Shi, Min
supporting information; experimental part, p. 2528 - 2533 (2010/07/15)
Diarylmethylenecycloalkanes were acetoxylated under the radical reaction conditions with PhI(OAc)2, I2, and TsNH2. Moreover, upon treating the products from the reactions of methylenecyclobutanes with N-bromosuccinimide (N
Oxidation by Cobalt(III) Acetate. Part 8. Effects of Substituents on Product Distributions in Oxidation of Aromatic Olefins by Cobalt(III) Acetate
Morimoto, Takashi,Hirano, Masao,Koyama, Tsuyoshi
, p. 1109 - 1116 (2007/10/02)
Oxidation of aromatic olefins by cobalt(III) acetate in acetic acid under nitrogen gave both allylic acetates and glycol monoacetates.Disubstituted olefins were oxidized by the oxidant to give predominantly allylic acetates.Glycol monoacetates were minor products except for the case of 1-phenylisobutene which was slowly oxidized to give the corresponding glycol monoacetate.In the oxidation of tri- and tetra-substituted olefins, the yield of glycol monoacetate increased at the expense of that of allylic acetate.A mechanism, in which the reaction proceeds through a Co-co-ordinated radical kation formed by an one-electron abstraction from olefin by cobalt(III) acetate, is suggested.
