105371-97-9Relevant academic research and scientific papers
A transition-metal-free Heck-type reaction between alkenes and alkyl iodides enabled by light in water
Liu, Wenbo,Li, Lu,Chen, Zhengwang,Li, Chao-Jun
supporting information, p. 6170 - 6174 (2015/06/08)
A transition-metal-free coupling protocol between various alkenes and non-activated alkyl iodides has been developed by using photoenergy in water for the first time. Under UV irradiation and basic aqueous conditions, various alkenes efficiently couple with a wide range of non-activated alkyl iodides. A tentative mechanism, which involves an atom transfer radical addition process, for the coupling is proposed.
Substituent effects for the olefination of aldehydes by zirconium metalloazines
Arvanitis, Georgia M.,Schwartz, Jeffrey
, p. 421 - 423 (2008/10/08)
The reaction between Zr(IV) metalloazines and aldehydes affords unsymmetrical olefins and azines. Relative rates for formation of these species (and corresponding yields) were found to depend on the electron-donating ability of the metalloazine and on the electron-accepting ability of the aldehyde. Second-order rate constants were determined, and a reaction mechanism for olefin synthesis is proposed based on observed electronic effects.
