128752-83-0Relevant academic research and scientific papers
Oxidative addition of dimethyl malonate to styrenes mediated by cerium(IV) ammonium nitrate: Some novel observations
Nair, Vijay,Mathew, Jessy,Nair, Latha G.
, p. 3053 - 3064 (1997)
The oxidative addition of dimethyl malonate to ring substituted styrenes leads to the formation of substituted dimethyl (2-oxo-2-phenylethyl) malonate and methyl 2-oxo-5-phenyltetrahydrofuran-3-carboxylate along with small amounts of substituted dimethyl [2-(nitrooxy)-2-phenylethyl] malonate and dimethyl 2-methoxy-2-phenylethyl) malonate. A tentative mechanism which supports the formation of these products is also presented.
Relative Rates for the Addition Reactions of the Malonyl Radical to Substituted Styrenes Induced by Cerium(IV) Ammonium Nitrate and Tributyltin Hydride. A Comparison
Baciocchi, Enrico,Giese, Bernd,Farshchi, Hassan,Ruzziconi, Renzo
, p. 5688 - 5691 (2007/10/02)
The relative rates for the addition reactions of the malonyl radical to substituted styrenes induced by cerium(IV) ammonium nitrate (CAN) and tributyltin hydride have been determined.The two processes exhibit practically identical ρ+ values (-1.05 and -1.06), thus suggesting that the coordination between the metal and the radical does not play a significant role in the CAN-promoted oxidative additions.
