摘要
A radical-mediated oxidative cross-coupling of readily accessible α-alkylated styrenes with 1,3-dicarbonyl compounds utilizing a combination of Cu(OAc)2 and air as a catalytic system is described. Rather than requiring α-halocarbonyl compounds, this efficient approach enables direct installation of tertiary functionalized alkyl motifs to olefins with simple carbonyl derivatives. The novel protocol is characterized with high allylic selectivities via a competing β-H elimination. Both radical-clock and -trapping experiments provided clear-cut evidence for the intermediacy of an α-keto carbon-centered radical.
源语言 | 英语 |
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页(从-至) | 4032-4035 |
页数 | 4 |
期刊 | Organic Letters |
卷 | 20 |
期 | 13 |
DOI | |
出版状态 | 已出版 - 6 7月 2018 |