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钴催化的通过质子耦合电子转移辅助的芳烃的区域选择性邻位 C(sp)-H 键硝化反应。

Cobalt-Catalyzed Regioselective Ortho C(sp)-H Bond Nitration of Aromatics through Proton-Coupled Electron Transfer Assistance.

机构信息

Medicinal Chemistry Division, Indian Institute of Integrative Medicine (CSIR) , Jammu 180001, India.

Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER) , Sector 67, S.A.S. Nagar, 160 062 Punjab, India.

出版信息

J Org Chem. 2017 Jul 21;82(14):7234-7244. doi: 10.1021/acs.joc.7b00808. Epub 2017 Jul 11.

Abstract

A cobalt-catalyzed proton-coupled electron transfer (PCET) mediated regioselective ortho-specific nitration of aromatic C(sp)-H bonds using chelation-assisted removable vicinal diamine directing groups was developed. The reaction proceeded under mild conditions in the presence of Co(OAc)·4HO as the catalyst with AgNO utilized as the nitro source as well as terminal oxidant in the presence of O as an external oxidant. No external base or additives were required for this process. Controlled experiments and mechanistic investigations with DFT calculations revealed that the reaction proceeds through a PCET promoted nitro functional group transfer pathway. Moreover, the produced compounds are valuable and pharmaceutically quite relevant.

摘要

发展了一种钴催化的质子耦合电子转移(PCET)介导的区域选择性芳环 C(sp)-H 键邻位特异性硝化反应,使用螯合辅助可去除的邻位二胺导向基团。在温和条件下,以 Co(OAc)·4HO 作为催化剂,AgNO 作为硝基源和末端氧化剂,在 O 作为外部氧化剂的存在下,该反应可以顺利进行。该过程不需要外部碱或添加剂。通过控制实验和 DFT 计算的机理研究表明,反应通过 PCET 促进的硝基官能团转移途径进行。此外,生成的化合物具有较高的价值,在药物方面具有重要的相关性。

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