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- W2331567155 abstract "The ability to convert simple and common substrates into fluoroalkyl derivatives under mild conditions remains an important goal for medicinal and agricultural chemists. One representative example of a desirable transformation involves the conversion of aromatic and heteroaromatic ketones and aldehydes into aryl and heteroaryl β,β,β-trifluoroethylarenes and -heteroarenes. The traditional approach for this net transformation involves stoichiometric metals and/or multistep reaction sequences that consume excessive time, material, and labor resources while providing low yields of products. To complement these traditional strategies, we report a one-pot metal-free decarboxylative procedure for accessing β,β,β-trifluoroethylarenes and -heteroarenes from readily available ketones and aldehydes. This method features several benefits, including ease of operation, readily available reagents, mild reaction conditions, high functional-group compatibility, and scalability." @default.
- W2331567155 created "2016-06-24" @default.
- W2331567155 creator A5024129726 @default.
- W2331567155 creator A5041733788 @default.
- W2331567155 creator A5042662807 @default.
- W2331567155 creator A5070642346 @default.
- W2331567155 date "2014-07-15" @default.
- W2331567155 modified "2023-10-18" @default.
- W2331567155 title "Metal-Free Trifluoromethylation of Aromatic and Heteroaromatic Aldehydes and Ketones" @default.
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- W2331567155 doi "https://doi.org/10.1021/jo501289v" @default.
- W2331567155 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4120972" @default.