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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Efficient Methods for the Synthesis of Thieno(3,2-b)thiophene and Thieno(3,2-b)furan Derivatives
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Efficient Methods for the Synthesis of Thieno(3,2-b)thiophene and Thieno(3,2-b)furan Derivatives

机译:噻吩(3,2-B)噻吩和噻吩(3,2-B)呋喃衍生物合成的有效方法

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摘要

A novel approach to the synthesis of thieno[3,2-b] thiophenes and thieno[3,2-b]furans bearing various substituents from readily accessible starting materials has been developed. The methodology is based on C- and O-alkylation of ethyl 4-hydroxy-2-methylthiophene-3-carboxylate with a-halo ketones, followed by cyclization. A great interest has been concentrated on thieno[3,2-b]thiophene and thieno[3,2-b]furan derivatives, because of both their biological activity and their potential elec-trooptical properties for use as molecular devices. These compounds could be used as aryl residues for di-hetarylethenes that possess good photochromic properties; however, research in this area has been impeded by the lack of efficient synthetic routes to thieno[3,2-b]thiophene and thieno[3,2-b]furan derivatives.
机译:已经开发了一种新的噻吩合成的新方法[3,2-b]噻吩和噻吩并[3,2-b]呋喃,其携带各种取代基的易于可接近的原料。 该方法基于乙基4-羟基-2-甲基噻吩-3-羧酸甲酸酯的C-和O-烷基化与卤素酮,然后环化。 由于它们的生物活性及其潜在的ELEC-Trophoptical属性,噻吩和噻吩和噻吩和噻吩并在噻吩和噻吩和噻吩(Thieno [3,2-B]呋喃衍生物中)浓郁的兴趣。 这些化合物可用作具有良好光致变色特性的二甲丙烯烯的芳基残基; 然而,通过缺乏高效的合成途径和Thieno [3,2-B]呋喃衍生物,缺乏高效的合成途径,已经阻碍了该领域的研究。

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