氟磺酸香豆素在水中无铜Sonogashira偶联:一种合成新型炔基香豆素衍生物的改进方法

IF 2 3区 化学 Q2 CHEMISTRY, ORGANIC
M. Rajini, Venkatachalam Munusamy, Muthipeedika Nibin Joy, Grigory V. Zyryanov
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引用次数: 0

摘要

本文报道了一种通过探索无铜Sonogashira偶联反应来合成一系列炔基香豆素衍生物的改进、原子经济和生态友好的方法。使用水作为溶剂,并使用氟硫酸香豆素作为原子经济的亲电偶联伙伴,证明了这种改进方法的合成实用性。氟硫酸香豆素比其他假卤化物基离去基的优越性已在后期进行了比较研究。通过计算最后阶段产物形成的e因子,实现了我们改进的合成方案的环境友好性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Copper-Free Sonogashira Coupling of Coumarin Fluorosulfates in Water: A Modified Approach for the Synthesis of Novel Alkynyl Coumarin Derivatives

Copper-Free Sonogashira Coupling of Coumarin Fluorosulfates in Water: A Modified Approach for the Synthesis of Novel Alkynyl Coumarin Derivatives

A modified, atom-economical, and ecofriendly approach developed for synthesizing an array of alkynyl coumarin derivatives by exploring the copper-free Sonogashira coupling reaction is reported herein. The usage of water as a solvent, along with the utilization of coumarin fluorosulfate as an atom-economical electrophilic coupling partner, demonstrates the synthetic utility of this modified methodology. The superiority of coumarin fluorosulfate over other pseudohalide-based leaving groups has been realized by performing a comparative study at a later stage. The environmental friendliness of our modified synthetic protocol has been realized by calculating the E-factor for the formation of products at the final stage.

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来源期刊
Journal of Heterocyclic Chemistry
Journal of Heterocyclic Chemistry 化学-有机化学
CiteScore
5.20
自引率
4.20%
发文量
177
审稿时长
3.9 months
期刊介绍: The Journal of Heterocyclic Chemistry is interested in publishing research on all aspects of heterocyclic chemistry, especially development and application of efficient synthetic methodologies and strategies for the synthesis of various heterocyclic compounds. In addition, Journal of Heterocyclic Chemistry promotes research in other areas that contribute to heterocyclic synthesis/application, such as synthesis design, reaction techniques, flow chemistry and continuous processing, multiphase catalysis, green chemistry, catalyst immobilization and recycling.
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