Polystyrenesulfonate-catalyzed synthesis of novel pyrroles through Paal-Knorr reaction.

Mandira Banik, Bianca Ramirez, Ashwini Reddy, Debasish Bandyopadhyay, Bimal K Banik
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引用次数: 10

Abstract

Background: The classical Paal-Knorr reaction is one of the simplest and most economical methods for the synthesis of biologically important and pharmacologically useful pyrrole derivatives.

Results: Polystyrenesulfonate-catalyzed simple synthesis of substituted pyrroles following Paal-Knorr reaction has been accomplished with an excellent yield in aqueous solution. This method also produces pyrroles with multicyclic polyaromatic amines.

Conclusions: The present procedure for the synthesis of N-polyaromatic substituted pyrroles will find application in the synthesis of potent biologically active molecules.

Abstract Image

聚苯乙烯磺酸催化Paal-Knorr反应合成新型吡咯。
背景:经典Paal-Knorr反应是合成具有重要生物学意义和药理意义的吡咯衍生物的最简单、最经济的方法之一。结果:在Paal-Knorr反应的基础上,聚苯磺酸盐催化合成了取代吡咯,收率高。这种方法也可以产生含有多环多芳胺的吡咯。结论:n -多芳香取代吡咯的合成方法将在合成具有强生物活性的分子中得到应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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