Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 12, Issue 10, Pages 1547-1550Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3ob42486c
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Funding
- NRF Nano Material Technology Development Program [2012M3A7B4049652]
- KETEP Human Resources Development Program [20124010203270]
- NRF Basic Science Research Program [2009-0094023]
- Korea Evaluation Institute of Industrial Technology (KEIT) [20124010203270] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
- National Research Foundation of Korea [2012M3A7B4049652] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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We found that chemoselectivity of the crossed acyloin product is controlled by the adjustment of the aromatic aldehyde/aliphatic aldehyde ratio. Moreover, we observed the persistent catalytic activity of the homogeneous NHC catalyst in a solution due to NHC catalyst robustness.
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