Redox Reactions in Palladium Catalysis: On the Accelerating and/or Inhibiting Effects of Copper and Silver Salt Additives in Cross-Coupling Chemistry Involving Electron-rich Phosphine Ligands

被引:77
作者
Aufiero, Marialuisa [1 ]
Proutiere, Fabien [1 ]
Schoenebeck, Franziska [1 ]
机构
[1] ETH, Organ Chem Lab, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
copper; redox reactions; silver; Sonogashira; Suzuki; ARYL CHLORIDES; ROOM-TEMPERATURE; DIRECT ARYLATION; STILLE REACTION; COMPLEXES; TRANSITION; BOND; AMINATION; BROMIDES; ALKYNYL;
D O I
10.1002/anie.201202504
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Challenging a catalytic cycle: Pd 0 catalysts are readily oxidized by Cu and Ag salts to give dinuclear Pd I complexes and Cu I or Ag I cubanes (see scheme). The reactivities of the resulting Pd I dimers are consistent with several observations of additive effects in cross-coupling chemistry. The results indicate the possibility for alternative catalytic cycles involving dinuclear Pd I complexes over the currently accepted synergistic cycles involving Pd 0/Pd II intermediates and Cu or Ag. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:7226 / 7230
页数:5
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