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从铜卡宾和叔丁基亚硝酯原位生成腈氧化物:全取代异恶唑的合成。

In situ generation of nitrile oxides from copper carbene and tert-butyl nitrite: synthesis of fully substituted isoxazoles.

机构信息

Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China.

出版信息

Org Biomol Chem. 2018 Jul 7;16(25):4683-4687. doi: 10.1039/c8ob01067f. Epub 2018 Jun 12.

Abstract

Herein, we present a novel [3 + 2] cycloaddition reaction of β-keto esters with nitrile oxides, which were generated in situ from copper carbene and tert-butyl nitrite. This three-component reaction provides new methodology for the direct synthesis of fully substituted isoxazole derivatives, featuring mild reaction conditions, readily accessible starting materials and simple operation. The experimental studies and DFT calculations suggest that the reaction starts with the generation of the key intermediate nitrile oxides, followed by a [3 + 2] cycloaddition reaction of β-keto esters to give the final isoxazole products.

摘要

在此,我们提出了一种β-酮酯与腈氧化物的新型[3 + 2]环加成反应,其中腈氧化物是由铜卡宾和叔丁基亚硝酸酯原位生成的。该三组分反应为完全取代的异噁唑衍生物的直接合成提供了新的方法,具有反应条件温和、起始原料易得和操作简单的特点。实验研究和 DFT 计算表明,反应首先生成关键中间体腈氧化物,然后β-酮酯进行[3 + 2]环加成反应得到最终的异噁唑产物。

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