A Tunable Class of Chiral Cp Ligands for Enantioselective Rhodium(III)-Catalyzed C-H Allylations of Benzamides

被引:393
作者
Ye, Baihua [1 ]
Cramer, Nicolai [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Lab Asymmetr Catalysis & Synth, Inst Chem Sci & Engn, CH-1015 Lausanne, Switzerland
基金
瑞士国家科学基金会; 欧洲研究理事会;
关键词
CYCLOPENTADIENYL LIGANDS; ASYMMETRIC-SYNTHESIS; 2+2+2 CYCLOADDITION; COMPLEXES; COBALT; RHODIUM; ACCESS; BINAPHTHYLCYCLOPENTADIENE; METALATION; ACTIVATION;
D O I
10.1021/ja311956k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The lack of robust and tunable chiral versions of cyclopentadienyl (Cp) ligands hampers progress in the development of catalytic asymmetric versions of a myriad of reactions catalyzed by this ubiquitous ligand. Herein, we describe of a class of chiral Cp ligands with tunable steric parameters. Coordinated to transition metals, the ligand creates a well-defined chiral pocket, able to imprint its chirality onto the metal. The corresponding Rh complexes are shown to be excellent catalysts for enantioselective allylation of N-methoxybenzamides via directed C-H functionalizations at very mild conditions. The obtained enantioselectivities are excellent and demonstrate the viability of chiral Cp complexes as selective transition metal catalysts.
引用
收藏
页码:636 / 639
页数:4
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