Abstract
An efficient tertiary alkylation reaction of olefins with 1,3-dicarbonyl compounds was developed by virtue of copper catalyst without the use of expensive ligands or additives. In contrast to alkyl Heck-type reaction, alkyl halide is not required. Notably, by varying the nitrogen and air atmosphere, the reaction selectively produces alkylation and alkylation-oxygenation products, respectively. Initial investigations revealed that an α-carbonyl alkyl radical species might be involved in the process.
Original language | English |
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Pages (from-to) | 1607-1611 |
Number of pages | 5 |
Journal | Organic Letters |
Volume | 21 |
Issue number | 6 |
DOIs | |
Publication status | Published - Mar 15 2019 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2019 American Chemical Society.
ASJC Scopus Subject Areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry