80754-07-0Relevant academic research and scientific papers
Selectfluor-mediated regioselective nucleophilic functionalization of N-heterocycles under metal- and base-free conditions
Xie, Long-Yong,Qu, Jie,Peng, Sha,Liu, Kai-Jian,Wang, Zheng,Ding, Man-Hua,Wang, Yi,Cao, Zhong,He, Wei-Min
supporting information, p. 760 - 764 (2018/02/14)
A practical and environmentally attractive methodology for the direct diversification of N-heterocycles at ambient temperature under open-air conditions was developed. The obvious advantage of the process is that no toxic reagent, transition metal, base or other additive is employed, thus greatly reducing costs, facilitating post-reaction neutralization and purification and minimizing the environmental impact.
Hydrogen Atom Transfer Oxidation of Primary and Secondary Alcoholates into Aldehydes and Ketones by Aromatic Halides in Liquid Ammonia. A New Electrochemically Induceable Reaction
Amatore, Christian,Badoz-Lambling, Janine,Bonnel-Huyghes, Claudine,Pinson, Jean,Saveant, Jean Michel,Thiebault, Andre
, p. 1979 - 1986 (2007/10/02)
It is possible to induce the oxidation of alcoholates into the corresponding carbonyl compounds by electrochemical reduction of aromatic halides in liquid ammonia, i.e., to electrochemically trigger the reaction ArX + >CH-O- -> ArH + >C=O + X-.H-Atom transfer from the acoholate to the aryl radical formed upon reduction of the aryl halide appears as the key step of the oxidation process.The ketyl anion radical thus formed can be oxidized into the parent carbonyl compound, remain electrochemically stable, or be reduced into the dianion depending upon the location of the two corresponding standard potentials toward the reduction potential of the aryl halide.Electricity consumption thus tends toward 0, 1, and 2 F/mol for the three cases, respectively.The reactions competing with H-atom transfer, thus lowering the efficiency of the electrochemical inducement of the oxidation process, are electron transfer to the aryl radical which occur at the electrode surface and/or in the solution.These will play the role of termination steps for the corresponding chain system involving homogeneous initiation of the reaction.The kinetic analysis of the competition between H-atom transfer and homogeneous or heterogeneous electron transfer allows a detailed investigation of the reaction mechanism by electrochemical techniques such as cyclic voltammetry.This also leads to the determination of the rate constants of H-atom transfer of the alcoholate-aryl radical couple.
