Journal
ORGANIC CHEMISTRY FRONTIERS
Volume 9, Issue 3, Pages 715-719Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1qo01568k
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Funding
- National Natural Science Foundation of China [21790333, 21925111]
- Strategic Priority Research Program of the CAS [XDPB14]
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A palladium-catalyzed tandem carbonylative lactonization and cycloaddition reaction has been developed, allowing efficient conversion of alkenes to various bridged lactones. The strategy can also be used for intramolecular tandem hydrocarbonylative lactonization and cycloaddition reactions to access more complex bridged lactones.
A palladium-catalyzed tandem carbonylative lactonization and cycloaddition reaction of 2-vinyl acetophenones with alkenes and CO has been established. This reaction enables an efficient conversion of the easily available alkenes to various bridged lactones through intermolecular cycloaddition. Furthermore, an intramolecular tandem hydrocarbonylative lactonization and cycloaddition reaction could also be established to access more complex bridged lactones by this strategy.
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