Electronically tunable N-heterocyclic carbeneligands: 1,3-diaryl vs. 4,5-diaryl substitution

Literature Information

Publication Date 2009-09-02
DOI 10.1039/B914732B
Impact Factor 6.222
Authors

James W. Ogle, Stephen A. Miller


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Abstract

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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