5- 氨基吡唑的有机催化歧化反应:4-Hydroxypyrazolines 的合成。

IF 3.3 2区 化学 Q1 CHEMISTRY, ORGANIC The Journal of Organic Chemistry Pub Date : 2024-07-11 DOI:10.1021/acs.joc.4c01160
Pradeep Natarajan, Subhashini V. Subramaniam and Saravanan Peruncheralathan*, 
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引用次数: 0

摘要

脱芳烃反应是一种基本化学反应,可生成复杂的三维杂环框架。我们首次披露了 5-aminopyrazoles 的有机催化脱芳烃反应,在原位生成的高价碘条件下,该反应生成了一系列结构多样化的 C4-羟基吡唑,产率≤95%。该方法还能通过分子内脱芳过程生成螺内酯。此外,我们还证明了底物定向还原生成的亚氨基吡唑啉可得到 4,5-二官能化吡唑啉的单一非对映异构体。机理研究表明,该反应是通过脱芳烃阳离子中间体进行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Organocatalytic Dearomatization of 5-Aminopyrazoles: Synthesis of 4-Hydroxypyrazolines

Dearomatization is a fundamental chemical reaction that affords complex three-dimensional heterocyclic frameworks. We disclose the first organocatalytic dearomatization of 5-aminopyrazoles, which yields a range of structurally diversified C4-hydroxylated pyrazolines with yields of ≤95% in <1.5 h at room temperature. This catalytic process is achieved using in situ-generated hypervalent iodine. The method also yields a spirolactone via an intramolecular dearomatization process. Furthermore, we demonstrate that substrate-directed reduction of the resulting iminopyrazoline leads to 4,5-difunctionalized pyrazoline as a single diastereomer. Mechanistic studies suggest that the reaction proceeds through a dearomatized cationic intermediate.

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来源期刊
The Journal of Organic Chemistry
The 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: The 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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