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Synfacts 2005(2): 0253-0253
DOI: 10.1055/s-2005-916113
DOI: 10.1055/s-2005-916113
Metal-Mediated Synthesis
© Georg Thieme Verlag Stuttgart · New York
Enantioselective Negishi Cross-Coupling of Secondary Benzylic Halides
F. O. Arp, G. C. Fu*
Massachusetts Institute of Technology, Cambridge, usa
Further Information
Publication History
Publication Date:
25 October 2005 (online)
Significance
Secondary benzylic halides can be efficiently reacted with primary alkylzinc bromides in the presence of chiral Ni-PyBox catalyst in DMA, giving the cross-coupling products in high yields and good enantioselectivities. Both enantiomers of a benzylic bromide can be converted into the same coupling product. 1-Chloroindanes are also suitable substrates for the reaction, although leading to lower yields of products. The reaction uses organozinc nucleophiles and therefore offers good functional group tolerance, including ketones, nitriles and phthalimide. This is one of the first reports of enantioselective alkyl-alkyl cross-coupling reactions.