Pd(0)-Catalyzed Diarylation of sp3C−H Bond in (2-Azaaryl)methanes
摘要:
A highly efficient and selective palladium-catalyzed diarylation of (2-azaaryl)methanes at the methyl group is described. Aryl chlorides proved reactive enough. A palladium eta(3)-azaallyl intermediate has been identified on the basis of DFT studies.
Reactions of 2-carbonyl- and 2-hydroxy(or methoxy)alkyl-substituted benzimidazoles with arenes in the superacid CF<sub>3</sub>SO<sub>3</sub>H. NMR and DFT studies of dicationic electrophilic species
作者:Dmitry S Ryabukhin、Alexey N Turdakov、Natalia S Soldatova、Mikhail O Kompanets、Alexander Yu Ivanov、Irina A Boyarskaya、Aleksander V Vasilyev
DOI:10.3762/bjoc.15.191
日期:——
Reactions of 2-carbonyl- and 2-hydroxy(or methoxy)alkylbenzimidazoles with arenes in the Brønsted superacid TfOH resulted in the formation of the corresponding Friedel–Crafts reaction products, 2-diarylmethyl and 2-arylmethyl-substituted benzimidazoles, in yields up to 90%. The reaction intermediates, protonated species derived from starting benzimidazoles in TfOH, were thoroughly studied by means