These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Nickel-catalyzed cross-coupling of alkyl zinc halides for the formation of C(sp(2))-C(sp(3)) bonds: scope and mechanism.
    Author: Phapale VB, Guisán-Ceinos M, Buñuel E, Cárdenas DJ.
    Journal: Chemistry; 2009 Nov 23; 15(46):12681-8. PubMed ID: 19847828.
    Abstract:
    Optimal conditions for a general Ni-catalysed Negishi cross-coupling of alkyl zinc halides with aryl, heteroaryl and alkenyl halides have been determined. These conditions allow the reaction to take place smoothly, with low catalyst loading, and in the presence of a wide variety of functional groups to afford products in good yields at room temperature. DFT studies on the mechanism support the occurrence of a catalytic cycle involving transmetalation of the alkyl zinc halide to Ni(I) followed by oxidative addition of the haloarene and C-C reductive elimination.
    [Abstract] [Full Text] [Related] [New Search]