Palladium(I) Dimer Enabled Extremely Rapid and Chemoselective Alkylation of Aryl Bromides over Triflates and Chlorides in Air

被引:78
作者
Kalvet, Indrek [1 ]
Sperger, Theresa [1 ]
Scattolin, Thomas [1 ]
Magnin, Guillaume [1 ]
Schoenebeck, Franziska [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Organ Chem, Landoltweg 1, D-52074 Aachen, Germany
基金
欧洲研究理事会;
关键词
homogeneous catalysis; chemoselectivity; Csp(2)-Csp(3) coupling; dimers; palladium; DINUCLEAR PD(I) COMPLEXES; CROSS-COUPLING REACTIONS; SELECTIVE FUNCTIONALIZATION; HALOGENATED NITROGEN; OXIDATIVE ADDITION; ALKYLZINC HALIDES; REACTIVITY; CATALYSTS; REAGENTS; ARENES;
D O I
10.1002/anie.201701691
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Disclosed herein is the first general chemo- and site-selective alkylation of C-Br bonds in the presence of COTf, C-Cl and other potentially reactive functional groups, using the air-, moisture-, and thermally stable dinuclear Pd-I catalyst, [Pd(mu-I)PtBu3](2). The bromo-selectivity is independent of the substrate and the relative positioning of the competing reaction sites, and as such fully predictable. Primary and secondary alkyl chains were introduced with extremely high speed (<5 min reaction time) at room temperature and under open-flask reaction conditions.
引用
收藏
页码:7078 / 7082
页数:5
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