新型天然苯并呋喃-1,3-噻唑烷-4-酮衍生物的合成及其抗氧化活性研究。

Bioorganicheskaia khimiia Pub Date : 2013-07-01
N A Abdel Latif, S H Abdel Hafez, L M Break
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引用次数: 0

摘要

本文描述了苯并呋喃-1,3-噻唑烷酮衍生物的合成。这些化合物是由菊石酮与芳香/脂肪胺缩合反应,再用巯基乙酸环化制备而成的。新合成的化合物使用众所周知的光谱工具(IR, 1H NMR和质谱)以及微量分析进行了表征。在生物筛选框架下,体外评估化合物的抗氧化活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of new benzofuran-1,3-thiazolidin-4-one derivatives from natural sources and study of their antioxidant activity.

Synthesis of benzofuran-1,3-thiazolidinone derivatives is described herein. These compounds were prepared via a concise and short route by condensation reaction of khellinone with aromatic/aliphatic amines followed by cyclization using thioglycolic acid. The newly synthesized compounds were characterized using the well known spectroscopic tools (IR, 1H NMR, and mass spectroscopy), as well as microanalysis. In frames of biological screening of the compounds, antioxidant activity was assessed in vitro.

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