Antifungal activity of solventlessly synthesized organomercurials.

M Kidwai, R Venkataramanan, B Dave
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引用次数: 3

Abstract

A series of new barbituryl/thiobarbituryl substituted organomercurial derivatives 3a-i have been synthesised from pyrimidine derivatives 1a-c and arylmercuric chloride 2a-c over K(2)CO(3) under microwave irradiations (MWI). This solventless synthesis apart from eliminating organic solvent from workup step, also gave improved yield as compared to the conventional heating, with reaction time reduced from hours to minutes. The prepared compounds were tested against A. niger and A. flavous for their antifungal activity and were found to posses good activity.

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无溶剂合成有机化合物的抗真菌活性。
以嘧啶衍生物1a-c和芳基氯化汞2a-c为原料,在K(2)CO(3)微波辐射下合成了一系列新的巴比妥基/硫代巴比妥基取代的有机汞衍生物3a-i。这种无溶剂合成除了消除了后续步骤中的有机溶剂外,与传统加热相比,收率也有所提高,反应时间从几小时缩短到几分钟。所制化合物对黑曲霉和黄曲霉的抑菌活性进行了测试,发现其具有良好的抑菌活性。
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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