Enantioselective imine hydrogenation with Ir diphosphine catalysts: fighting deactivation

被引:31
作者
Blaser, HU [1 ]
Pugin, B
Spindler, F
Togni, A
机构
[1] Solvias AG, WRO 1055 6, Basel, Switzerland
[2] ETH Honggerberg, Inorgan Chem Lab, CH-8093 Zurich, Switzerland
关键词
Ir diphosphine complexes; imine hydrogenation; catalyst deactivation; immobilized catalysts; bimetallic catalyst precursors;
D O I
10.1016/S1631-0748(02)01391-7
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
While Ir diphosphine complexes are very active catalysts for the enantioselective hydrogenation of imines with good to excellent enantioselectivity, their deactivation is often a serious problem, leading to low catalyst productivity. Our study describes attempts to stabilize Ir catalysts with diop, bdpp and bppm ligands for the hydrogenation of different imines. The best results were obtained with complexes immobilised on silica gel and with bimetallic W-Ir and Mo-Ir complexes. In most cases, enantiomeric excesses as well as initial rates were only slightly affected while the stability of the catalysts was enhanced significantly.
引用
收藏
页码:379 / 385
页数:7
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