Efficient C-N and C-S bond formation using the highly active [Ni(allyl)Cl(IPr*OMe)] precatalyst

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Martin, Anthony R. and Nelson, David and Meiries, Sébastien and Slawin, Alexandra M.Z. and Nolan, Steven P. (2014) Efficient C-N and C-S bond formation using the highly active [Ni(allyl)Cl(IPr*OMe)] precatalyst. European Journal of Organic Chemistry. ISSN 1434-193X (https://doi.org/10.1002/ejoc.201402022)

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Abstract

Two new [Ni(allyl)Cl(NHC)] complexes with the bulky yet flexible N-heterocyclic carbene (NHC) ligands IPr* {N,N'-bis[2,6-bis(diphenylmethyl)-4-methylphenyl]imidazole-2-ylidene} and IPr*OMe {N,N'-bis[2,6-bis(diphenylmethyl)-4-methoxyphenyl]imidazol-2-ylidene} are reported. These complexes were employed in the amination and sulfination of aryl halide species and were shown to perform well in these reactions, which typically required less than half as much catalyst as previous state-of-the-art nickel complexes.

ORCID iDs

Martin, Anthony R., Nelson, David ORCID logoORCID: https://orcid.org/0000-0002-9461-5182, Meiries, Sébastien, Slawin, Alexandra M.Z. and Nolan, Steven P.;
  • Item type:Article
    ID code:47882
    Dates:
    Date
    Event
    7 March 2014
    Published
    7 March 2014
    Published Online
    2014
    Accepted
    Subjects:Science > Chemistry
    Department:UNSPECIFIED
    Depositing user: Pure Administrator
    Date deposited:07 May 2014 12:53
    Last modified:11 Nov 2024 10:41
    Related URLs:
    URI:https://strathprints.strath.ac.uk/id/eprint/47882
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