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Synfacts 2010(3): 0318-0318
DOI: 10.1055/s-0029-1219401
DOI: 10.1055/s-0029-1219401
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
Nickel-Catalyzed Asymmetric Hydrovinylation at Room Temperature
N. Lassauque, G. Franciò*, W. Leitner*
RWTH Aachen, Germany
Further Information
Publication History
Publication Date:
18 February 2010 (online)
![](https://www.thieme-connect.de/media/synfacts/201003/lookinside/thumbnails/10.1055-s-0029-1219401-1.jpg)
Significance
Asymmetric hydrovinylation holds a special place in catalysis as it was an early example of asymmetric C-C bond formation. Chiral phosphoramidite ligands, such as L1 and L2, have been successfully employed in nickel-catalyzed hydrovinylations, but the reactions usually required low temperature (typically -78 ˚C) in order to obtain good chemo- and enantioselectivities. The authors reported a highly efficient and selective hydrovinylation protocol at room temperature using ligands of the type L3-5.