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- 杂环卡宾催化醛与三氟甲磺酸重氮碘鎓盐的环化反应:便捷合成2,5-二取代-1,3,4-恶二唑

-Heterocyclic Carbene-Catalyzed Cyclization of Aldehydes with α-Diazo Iodonium Triflate: Facile Access to 2,5-Disubstituted 1,3,4-Oxadiazoles.

作者信息

Huang Hang, Zou Xianghua, Cao Si, Peng Zhihong, Peng Yingying, Wang Xi

机构信息

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Advanced Catalytic Engineering Research Center of the Ministry of Education, Hunan University, Changsha 410082, P. R. China.

出版信息

Org Lett. 2021 Jun 4;23(11):4185-4190. doi: 10.1021/acs.orglett.1c01128. Epub 2021 May 14.

Abstract

Herein, we report a novel organocatalytic process for synthesis of complex 1,3,4-oxadiazoles from readily accessible aldehydes. By exploiting the nucleophilicity of the putative Breslow intermediate and the inherent electrophilicity of α-diazo iodonium triflate, we have found that -heterocyclic carbene catalyst promotes efficient cyclization of various aldehydes and α-diazo iodonium triflates. The reaction proceeds under mild conditions with a wide range of functional group tolerance. The heterocyclic products can be readily further functionalized, rendering the protocol highly valuable.

摘要

在此,我们报道了一种由易于获得的醛合成复杂1,3,4-恶二唑的新型有机催化方法。通过利用假定的布雷斯洛中间体的亲核性和α-重氮三氟甲磺酸碘鎓盐固有的亲电性,我们发现杂环卡宾催化剂能促进各种醛与α-重氮三氟甲磺酸碘鎓盐的高效环化反应。该反应在温和条件下进行,对各种官能团具有广泛的耐受性。杂环产物可很容易地进一步官能化,使得该方法具有很高的价值。

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