Chirila Paula G, Adams Joshua, Dirjal Amir, Hamilton Alex, Whiteoak Christopher J
Department of Biosciences and Chemistry and the, Biomolecular Sciences Research Centre (BMRC), Sheffield Hallam University, Sheffield, S1 1WB, UK.
Chemistry. 2018 Mar 7;24(14):3584-3589. doi: 10.1002/chem.201705785. Epub 2018 Feb 12.
A Cp*Co -catalyzed C-H functionalization of benzamide substrates with α,β-unsaturated ketones has been optimized, providing a facile route towards aliphatic ketone products. When employing α,β-unsaturated aldehydes as coupling partners, under the optimized protocol, a cascade reaction forming azepinones has also been developed. Finally, DFT studies have demonstrated how stabilization of a metallo-enol intermediate when employing α,β-unsaturated ketones is the driving force leading to the observed aliphatic ketone product rather than olefinic products reported using α,β-unsaturated esters as coupling partners.
一种使用Cp*Co催化苯甲酰胺底物与α,β-不饱和酮进行C-H官能化反应的方法已得到优化,为制备脂肪族酮产物提供了一条简便途径。当使用α,β-不饱和醛作为偶联伙伴时,在优化的反应条件下,还开发了一种形成氮杂环庚三酮的串联反应。最后,密度泛函理论(DFT)研究表明,在使用α,β-不饱和酮时,金属烯醇中间体的稳定性是导致观察到脂肪族酮产物而非使用α,β-不饱和酯作为偶联伙伴时报道的烯烃产物的驱动力。