An Electrophilic Approach to the Palladium-Catalyzed Carbonylative C-H Functionalization of Heterocycles

被引:55
|
作者
Tjutrins, Jevgenijs [1 ]
Arndtsen, Bruce A. [1 ]
机构
[1] McGill Univ, Dept Chem, Montreal, PQ H3A 0B8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
BOND FUNCTIONALIZATION; DIRECT ARYLATION; PHOTOCHEMICAL CARBONYLATION; ARYL BROMIDES; ACTIVATION; CARBOXYLATION; BENZENE; ACID; MECHANISM;
D O I
10.1021/jacs.5b07098
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A palladium-catalyzed approach to intermolecular carbonylative C H functionalization is described. This transformation is mediated by (PBu3)-Bu-t-coordinated palladium catalyst and allows the derivatization of a diverse range of heterocycles, including pyrroles, indoles, imidazoles, benzoxazoles, and furans. Preliminary studies suggest that this reaction may proceed via the catalytic formation of highly electrophilic intermediates. Overall, this provides with an atom-economical and general synthetic route to generate aryl-(hetero)aryl ketones using stable reagents (aryl iodides and CO) and without the typical need to exploit pre-metalated heterocycles in carbonylative coupling chemistry.
引用
收藏
页码:12050 / 12054
页数:5
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