Journal
ORGANIC CHEMISTRY FRONTIERS
Volume 4, Issue 6, Pages 1074-1078Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7qo00111h
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Funding
- National Natural Science Foundation of China [21632005, 21472083]
- Nanjing University
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An effective palladium-catalyzed sequential carbonylation of olefins with formic acid is described. Ketones and the corresponding alpha,beta-enones can be obtained with up to 90% yield. The reaction process is operationally simple and requires no toxic CO.
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