<i>N</i>-Hydroxyphthalimide-Mediated Electrochemical Iodination of Methylarenes and Comparison to Electron-Transfer-Initiated C–H Functionalization
作者:Mohammad Rafiee、Fei Wang、Damian P. Hruszkewycz、Shannon S. Stahl
DOI:10.1021/jacs.7b09744
日期:2018.1.10
electrochemical method has been developed for selective benzylic iodination of methylarenes. The reactions feature the first use of N-hydroxyphthalimide as an electrochemical mediator for C-H oxidation to nonoxygenated products. The method provides the basis for direct (in situ) or sequential benzylation of diverse nucleophiles using methylarenes as the alkylating agent. The hydrogen-atom transfer mechanism for
Rozwadowska, Maria D.; Wysocka, Waleria, Polish Journal of Chemistry, 1982, vol. 56, # 3, p. 533 - 536
作者:Rozwadowska, Maria D.、Wysocka, Waleria
DOI:——
日期:——
Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. 3. N-(substituted benzyl)-2,4,6-triphenylpyridiniums: effects of benzyl substitution on first- and second-order rates
作者:Alan R. Katritzky、Giuseppe Musumarra、Kumars Sakizadeh
DOI:10.1021/jo00332a014
日期:1981.9
ROZWADOWSKA, M. D.;WYSOCKA, W., POL. J. CHEM., 1982, 56, N 3, 533-535