Abstract
An efficient palladium-catalyzed cross-coupling of indium homoenolate with aryl halide is described. The reactions proceeded efficiently in DMA at 100 °C to afford the desired products of β-aryl ketones in moderate to good yields. Various important functional groups including COR, COOR, CHO, CN, OH, and NO2 can be well tolerated in the protocol.
Original language | English |
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Pages (from-to) | 422-425 |
Number of pages | 4 |
Journal | Organic Letters |
Volume | 13 |
Issue number | 3 |
DOIs | |
Publication status | Published - Feb 4 2011 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry