首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Intermolecular heterocyclization of alkynones with 2-mercaptoacetaldehyde under metal-free conditions: synthesis of 2,3-disubstituted thiophenes
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Intermolecular heterocyclization of alkynones with 2-mercaptoacetaldehyde under metal-free conditions: synthesis of 2,3-disubstituted thiophenes

机译:在无金属条件下用2-巯基乙醛进行炔烃的分子间杂环化:2,3-二取代噻吩的合成

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摘要

A concise and regioselective approach for the synthesis of 2,3-disubstituted thiophene derivatives has been developed. The synthetic strategy relies on the reaction of an in situ generated 2-mercaptoacetaldehyde with various alkynones. Furthermore, we calculated the energy gap between the HOMO and the LUMO orbitals of all compounds and observed that the introduction of a strong electron-withdrawing group decreased the HOMO-LUMO energy gap. (C) 2015 Elsevier Ltd. All rights reserved.
机译:已经开发了用于合成2,3-二取代的噻吩衍生物的简洁和区域选择性的方法。合成策略依赖于原位生成的2-巯基乙醛与各种炔烃的反应。此外,我们计算了所有化合物的HOMO和LUMO轨道之间的能隙,并观察到强吸电子基团的引入降低了HOMO-LUMO的能隙。 (C)2015 Elsevier Ltd.保留所有权利。

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