Highly efficient molybdenum-based catalysts for enantioselective alkene metathesis

Article

关键词: RING-CLOSING METATHESIS;    IMIDO ALKYLIDENE COMPLEXES;    OLEFIN-METATHESIS;    METAL-COMPLEXES;    TUNGSTEN;    AMINES;    ETHERS;    LIGAND;   

DOI  :  10.1038/nature07594

来源: SCIE

【 摘 要 】

Discovery of efficient catalysts is one of the most compelling objectives of modern chemistry. Chiral catalysts are in particularly high demand, as they facilitate synthesis of enantiomerically enriched small molecules that are critical to developments in medicine, biology and materials science(1). Especially noteworthy are catalysts that promote - with otherwise inaccessible efficiency and selectivity levels - reactions demonstrated to be of great utility in chemical synthesis. Here we report a class of chiral catalysts that initiate alkene metathesis(1) with very high efficiency and enantioselectivity. Such attributes arise from structural fluxionality of the chiral catalysts and the central role that enhanced electronic factors have in the catalytic cycle. The new catalysts have a stereogenic metal centre and carry only monodentate ligands; the molybdenum- based complexes are prepared stereoselectively by a ligand exchange process involving an enantiomerically pure aryloxide, a class of ligands scarcely used in enantioselective catalysis(2,3). We demonstrate the application of the new catalysts in an enantioselective synthesis of the Aspidosperma alkaloid, quebrachamine, through an alkene metathesis reaction that cannot be promoted by any of the previously reported chiral catalysts.

【 授权许可】

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