Journal
CHEMICAL SCIENCE
Volume 6, Issue 8, Pages 4973-4977Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5sc01589h
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Funding
- ERC (Advanced Researcher award-FUNCAT)
- EPSRC [EP/J011053/1]
- King Saud University
- Royal Society Wolfson Research Merit Award
- EPSRC [EP/J011053/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/J011053/1] Funding Source: researchfish
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The first nickel catalyzed deprotonative cross coupling between C(sp(3))-H bonds and aryl chlorides is reported, allowing the challenging arylation of benzylimines in the absence of directing group or stoichiometric metal activation. This methodology represents a convenient access to the (diarylmethyl)amine moiety, which is widespread in pharmaceutically relevant compounds.
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