Davis Christopher W, Li Yanrong, Zhang Yu, Siddiqi Zohaib, Liu Peng, Sarlah David
Roger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, Illinois 61801, United States.
Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, United States.
ACS Catal. 2024 Jul 5;14(13):10132-10137. doi: 10.1021/acscatal.4c02656. Epub 2024 Jun 20.
We have achieved the arenophile-mediated, copper-catalyzed dearomative -1,2-carboamination of nonactivated arenes with alkyl organometallic nucleophiles. This simple and practical procedure was used to prepare diverse, stereochemically rich alkylated cyclohexadienes from readily available arenes. Synthetic utility was demonstrated through the rapid preparation of complex small molecules difficult to access by conventional routes. Finally, we conducted DFT studies to explore the catalytic process, including a study of the reaction pathway and an examination of the divergent regioselectivity observed with substituted arenes.
我们实现了在嗜芳烃介导、铜催化下,未活化芳烃与烷基有机金属亲核试剂进行脱芳构化-1,2-碳胺化反应。这一简单实用的方法用于从易得的芳烃制备多样的、立体化学丰富的烷基化环己二烯。通过快速制备传统路线难以获得的复杂小分子,证明了该方法的合成实用性。最后,我们进行了密度泛函理论(DFT)研究以探索催化过程,包括反应途径的研究以及对取代芳烃所观察到的不同区域选择性的考察。