Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000131.xml
Synfacts 2009(3): 0285-0285
DOI: 10.1055/s-0028-1087782
DOI: 10.1055/s-0028-1087782
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
Nickel-Catalyzed Cross-Coupling of α-Bromoketones with Arylzinc Reagents
P. M. Lundin, J. Esquivias, G. C. Fu*
Massachusetts Institute of Technology, Cambridge, USA
Further Information
Publication History
Publication Date:
19 February 2009 (online)

Significance
This paper described the NiCl2˙glyme/(+)-ligand catalyzed cross-coupling reaction of arylzinc with racemic secondary α-bromoketones. The resulting α-aryl ketones were obtained in excellent yields and good to excellent enantioselectivities. Remarkably, the unusually mild reaction conditions (-30 ˚C and no activators) allowed the generation of potentially labile tertiary stereocenters.