Chiral Cyclopentadienyl Iridium(III) Complexes Promote Enantioselective Cycloisomerizations Giving Fused Cyclopropanes

被引:64
作者
Dieckmann, Michael [1 ]
Jang, Yun-Suk [1 ]
Cramer, Nicolai [1 ]
机构
[1] EPFL SB ISIC LCSA, Lab Asymmetr Catalysis & Synth, CH-1015 Lausanne, Switzerland
基金
欧洲研究理事会;
关键词
asymmetric catalysis; cycloisomerization; cyclopentadienyl ligands; enantioselectivity; iridium; CATALYZED ASYMMETRIC CYCLOISOMERIZATION; C-H FUNCTIONALIZATIONS; ENANTIOMERICALLY PURE; IRIDIUM(I)-CATALYZED CYCLOISOMERIZATION; PTCL2-MEDIATED CYCLOISOMERIZATION; ENYNE CYCLOISOMERIZATION; TETHERED 1,6-ENYNES; AXIAL CHIRALITY; 1ST APPLICATION; GOLD CATALYSIS;
D O I
10.1002/anie.201506483
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The cyclopentadienyl (Cp) group is a very important ligand for many transition-metal complexes which have been applied in catalysis. The availability of chiral cyclopentadienyl ligands (Cp-x) lags behind other ligand classes, thus hampering the investigation of enantioselective processes. We report a library of chiral (CpIrIII)-Ir-x complexes equipped with an atropchiral Cp scaffold. A robust complexation procedure reliably provides (CpIrIII)-Ir-x complexes with tunable counterions. In a proof-of-concept application, the iodide-bearing members are shown to be highly selective for enyne cycloisomerization reactions. The dehydropiperidine-fused cyclopropane products are formed in good yields and enantioselectivities.
引用
收藏
页码:12149 / 12152
页数:4
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