Ce(OTf)3催化炔基羧酸、异氰酸叔丁基和叠氮化物的多组分反应组装三唑-恶唑衍生物

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Ming Cao, Yi-Lin Fang, Ying-Chun Wang*, Xiao-Juan Xu, Zhi-Wei Xi, Shi Tang*
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引用次数: 14

摘要

研究了三氟化铈催化烷基羧酸、异氰酸叔丁酯和有机叠氮化物之间的多组分反应。在Ce(OTf)3 (10 mol %)存在下,1分子炔基羧酸与3分子叔丁基异氰化物在室温下通过三次有序异氰化物插入过程进行了化学选择性和区域选择性的级联反应,然后通过温度升高(100℃)进一步引发了由铯催化的炔基恶唑与有机叠氮化物之间的[3 + 2]环加成反应。从而导致多取代三唑-恶唑衍生物实用、省时、一锅操作。部分目标化合物对人胃癌细胞MGC803具有潜在的抗癌活性,IC50值低于20 μmol L-1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ce(OTf)3-Catalyzed Multicomponent Reaction of Alkynyl Carboxylic Acids, tert-Butyl Isocyanide, and Azides for the Assembly of Triazole–Oxazole Derivatives

Ce(OTf)3-Catalyzed Multicomponent Reaction of Alkynyl Carboxylic Acids, tert-Butyl Isocyanide, and Azides for the Assembly of Triazole–Oxazole Derivatives

Cerium(III) triflate-catalyzed multicomponent reactions between alkynyl carboxylic acids, tert-butyl isocyanide, and organic azides have been developed. In the presence of Ce(OTf)3 (10 mol %), the cascade reaction of one molecule of alkynyl carboxylic acid with three molecules of tert-butyl isocyanides proceeds chemoselectively and regioselectively via a triple and ordered isocyanide insertion process at room temperature, and then the cesium-catalyzed [3 + 2] cycloaddtion reaction between the resulted alkynyl oxazole and organic azides was further initiated by the temperature elevation (100 °C), thereby leading to multisubstituted triazole–oxazole derivatives in practical, time-saving, one-pot operations. Furthermore, some of the synthesized target compounds showed potential anticancer activities against MGC803 (human gastric cancer cell) with IC50 values below 20 μmol L–1.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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