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三组分反应合成多官能团化α-氰基噻吩的简便方法
Convenient Synthesis of Highly Functionalized α-Cyanothiophene Derivatives via Three-component Reaction
【摘要】 本文报道了一种利用多组分反应合成α-氰基噻吩的新方法.在碱存在条件下,β-二羰基化合物、二硫化碳和溴乙腈经过连续的多步反应,"一锅"合成多官能团化的α-氰基噻吩.该方法简洁,条件温和,产率高.
【Abstract】 A convenient one-pot synthesis of highly functionalized α-cyanothiophene derivatives(4) by three-component reactions was developed. In the presence of K2CO3,1,3-dicarbonyl compounds 1 reacted with CS2(2) and bromoacetonitrile(3) resulted in the formation of functionalized α-cyanothiophenes(4) in high yields. The simplicity of execution,mild conditions,ready availability of substrates and high yields,make this synthetic strategy considerably attractive for academic research and practical applications.
【关键词】 三组分反应;
α-氰基噻吩;
β-二羰基化合物;
α-羰基二硫缩烯酮;
【Key words】 Three-component reactions; α-Cyanothiophene; 1,3-Dicarbonyl compounds; α-Oxo ketene-(S,S)-acetals;
【Key words】 Three-component reactions; α-Cyanothiophene; 1,3-Dicarbonyl compounds; α-Oxo ketene-(S,S)-acetals;
【基金】 国家自然科学基金(批准号:20672019);东北师范大学青年基金(批准号:20060309)资助
- 【文献出处】 高等学校化学学报 ,Chemical Journal of Chinese Universities , 编辑部邮箱 ,2009年01期
- 【分类号】O626.12
- 【被引频次】2
- 【下载频次】181