Journal
ORGANOMETALLICS
Volume 29, Issue 23, Pages 6343-6349Publisher
AMER CHEMICAL SOC
DOI: 10.1021/om100746r
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Funding
- Singapore National Research Foundation [NRF-RF2008-05]
- Nanyang Technological University
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A C2-protected imidazolium salt that generates an abnormal N-heterocyclic carbene (NHC) was applied for the palladium-catalyzed Suzuki-Miyaura coupling reactions. The abnormal NHC precursor promoted the reactions while suppressing homocoupling of aryl boronic acid, which was observed with the corresponding normal NHC precursor. The related well-defined abnormal NHC-based palladium complexes also showed better activity than the normal NHC-based analogues, exhibiting faster reaction rates especially at the initial stage of the reaction.
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