摘要
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.
源语言 | 英语 |
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页(从-至) | 1607-1611 |
页数 | 5 |
期刊 | Organic Letters |
卷 | 21 |
期 | 6 |
DOI | |
出版状态 | 已出版 - 15 3月 2019 |