Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 38, Pages 5728-5730Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b914732b
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Funding
- National Science Foundation [CHE-0824305]
- University of Florida
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The catalytic activity of iridium-mediated transfer hydrogenation is readily tuned by electronic variation of the ligated tetraaryl-N-heterocyclic carbene and the installation of electron donating groups on the N-aryl substituents is more important than on the C-aryl substituents for effecting catalytic enhancement.
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