Huang Hang, Zou Xianghua, Cao Si, Peng Zhihong, Peng Yingying, Wang Xi
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.
Org Lett. 2021 Jun 4;23(11):4185-4190. doi: 10.1021/acs.orglett.1c01128. Epub 2021 May 14.
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.
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。