4.7 Article

Room Temperature Highly Enantioselective Nickel-Catalyzed Hydrovinylation

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 351, Issue 18, Pages 3133-3138

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.200900559

Keywords

asymmetric catalysis; C-C coupling; olefin dimerization; phosphoramidite ligands

Funding

  1. Deutsche Forschungsgemeinschaft [FR2487/1-1]

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At room temperature, nickel catalysts based on the new phosphoramidite (11bR)-N-[(S)-1-(naphthalen-1-yl)ethyl]-N-[(S)-1-(naphthalen-2yl)ethyl]dinaphtho[2,1'-d:1',2'-f] [1,3,2]dioxaphosphepin-4-amine provide excellent selectivities for 3-arylbut-1-enes (93-99%) with high enantioselectivities (90-95% ee) and TOFs (up to 8300 h(-1)) in the hydrovinylation of electron-rich and electron-poor vinylarenes. Within a few minutes, useful chiral building blocks and intermediates can be synthesized using this practical catalytic system.

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