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Synthesis of new heterocyclic thiazolidinone and azetidinone compounds and their anticancer activity

机译:新型杂环噻唑烷酮和氮杂环丁酮化合物的合成及其抗癌活性

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摘要

Thiazolidinones and azetidinones have been prepared by the reaction of various schiff bases with thioglycollic acid and chloroacetyl chloride respectively. The intermediate schiff bases were synthesised by the condensation of diaminobenzanilide with various aldehydes. The thiazolidinones and azetidinones were tested for their anticancer activity.
机译:噻唑烷酮和氮杂环丁酮已经通过各种席夫碱分别与巯基乙酸和氯乙酰氯的反应制备。中间席夫碱是通过二氨基苯甲酰苯胺与各种醛的缩合合成的。测试了噻唑烷酮和氮杂环丁酮的抗癌活性。

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