路易斯酸催化的 2-炔基苯胺和 2-甲酰基苯腈的融合 N-杂环级联合成:揭示 Iminoisoindoloindolone 及其衍生物。

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Journal of Organic Chemistry Pub Date : 2024-09-06 Epub Date: 2024-08-22 DOI:10.1021/acs.joc.4c01038
Pallav Jyoti Arandhara, Archana Chutia, Subhamoy Biswas, Anil K Saikia
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引用次数: 0

摘要

我们在此揭示了一种通过精心策划的级联反应合成结构融合的 6-亚氨基异吲哚啉酮的简化方法。在 TMSOTf 的催化作用下,这一过程将 2-炔基苯胺和 2-甲酰基苯甲腈完美地结合在一起,产生了这些化合物,而且产率极高,证明了我们方法的高效性。此外,这种合成策略的多功能性远远超出了单纯的合成,它为创造异吲哚啉酮和前所未有的二苯基苯并吡咯嗪异喹啉酮衍生物提供了途径,从而为化学创新领域开辟了新天地。此外,这种合成方法的战略优雅性还体现在它的放大生产潜力和在不同化学领域的适用性上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Lewis Acid-Catalyzed Cascade Synthesis of Fused <i>N</i>-Heterocycles from 2-Alkynylanilines and 2-Formylbenzonitriles: Unveiling Iminoisoindoloindolone and Its Derivatives.

A Lewis Acid-Catalyzed Cascade Synthesis of Fused N-Heterocycles from 2-Alkynylanilines and 2-Formylbenzonitriles: Unveiling Iminoisoindoloindolone and Its Derivatives.

We herein reveal a streamlined synthesis of structurally fused 6-iminoisoindoloindolones via a meticulously orchestrated cascade reaction. This process seamlessly intertwines 2-alkynylaniline and 2-formylbenzonitrile under the catalytic influence of TMSOTf, giving rise to these compounds in remarkable yields that stand as a testament to the efficiency of our approach. Moreover, the versatility of this synthetic strategy extends far beyond mere synthesis, offering a gateway to the creation of both isoindoloindolone and unprecedented diphenylbenzopyrrolizinoisoquinolinone derivatives, thereby opening new horizons in the realm of chemical innovation. Furthermore, the strategic elegance of this synthetic methodology is underscored by its potential for scale-up production and applicability across diverse chemical contexts.

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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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