Cp*Co(III)-catalyzed synthesis of isoquinolones via controlled annulation of primary arylamides with internal alkynes.

IF 2.9 3区 化学 Q1 CHEMISTRY, ORGANIC Organic & Biomolecular Chemistry Pub Date : 2024-11-22 DOI:10.1039/d4ob01693a
Saksham Mishra, Akanksha Singh Baghel, Amit Kumar
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引用次数: 0

摘要

在本研究中,我们首次提出了钴(III)催化的异喹诺酮类化合物的直接合成方法,该方法通过受控的氧化 C-H/N-H 环化反应,从容易获得的伯胺和内部炔烃中直接合成异喹诺酮类化合物。这一创新方案无需使用昂贵的过渡金属盐和外部助剂,只需生产出所需的单环化产物,同时还适用于多种底物。初步的机理研究强调了氧化铜在促进转化中的关键作用。此外,还对核心异喹啉酮环进行了外围修饰,以合成复杂的杂环系统。
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Cp*Co(III)-catalyzed synthesis of isoquinolones via controlled annulation of primary arylamides with internal alkynes.

In this study, we present the first cobalt(III)-catalyzed direct synthesis of isoquinolones from readily available primary arylamides and internal alkynes through a controlled oxidative C-H/N-H annulation reaction. This innovative protocol eliminates the need for expensive transition metal salts and external auxiliaries, producing the desired mono-annulated product exclusively while accommodating a wide range of substrates. Preliminary mechanistic studies highlight the critical role of copper oxide in facilitating the transformation. Additionally, peripheral modifications of the core isoquinolone rings have been performed to synthesize complex heterocyclic systems.

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来源期刊
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry 化学-有机化学
CiteScore
5.50
自引率
9.40%
发文量
1056
审稿时长
1.3 months
期刊介绍: The international home of synthetic, physical and biomolecular organic chemistry.
期刊最新文献
Base-mediated denitrative C3-alkylation of quinoxaline derivatives. Isolation and biomimetic synthesis of acylphloroglucinol meroterpenoids as anti-breast cancer agents from Dryopteris crassirhizoma. Synthesis of 3,5-bis(fluoroalkyl)pyrazoles/pyrazolines via [3 + 2] cycloaddition of di/trifluoroacetohydrazonoyl bromides and trifluoromethyl-substituted alkenes. Cp*Co(III)-catalyzed synthesis of isoquinolones via controlled annulation of primary arylamides with internal alkynes. Discovery of nostatin A, an azole-containing proteusin with prominent cytostatic and pro-apoptotic activity.
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