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一锅法铁催化醇和甲基芳烃氧化偶联合成 4-喹诺酮

One-Pot Synthesis of 4-Quinolone via Iron-Catalyzed Oxidative Coupling of Alcohol and Methyl Arene.

机构信息

Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.

Natural Products Research Institute, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.

出版信息

Org Lett. 2020 Nov 6;22(21):8382-8386. doi: 10.1021/acs.orglett.0c03011. Epub 2020 Oct 15.

Abstract

Herein, we describe the iron(III)-catalyzed oxidative coupling of alcohol/methyl arene with 2-amino phenyl ketone to synthesize 4-quinolone. Alcohols and methyl arenes are oxidized to the aldehyde in the presence of an iron catalyst and di--butyl peroxide, followed by a tandem process, condensation with amine/Mannich-type cyclization/oxidation, to complete the 4-quinolone ring. This method tolerates various kinds of functional groups and provides a direct approach to the synthesis of 4-quinolones from less functionalized substrates.

摘要

在这里,我们描述了铁(III)催化的醇/甲基芳基与 2-氨基苯甲酮的氧化偶联,以合成 4-喹诺酮。在铁催化剂和过氧化二叔丁基的存在下,醇和甲基芳基被氧化为醛,然后通过串联过程,与胺/曼尼希型环化/氧化缩合,完成 4-喹诺酮环。该方法耐受各种官能团,并提供了一种直接从低官能化底物合成 4-喹诺酮的方法。

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