首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis of new Schiff bases and polycyclic fused thiopyranothiazoles containing 4,6-dichloro-1,3,5-triazine moiety
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Synthesis of new Schiff bases and polycyclic fused thiopyranothiazoles containing 4,6-dichloro-1,3,5-triazine moiety

机译:合成新的席夫碱和含有4,6-二氯-1,3,5-三嗪部分的多环稠合噻吩并噻唑

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摘要

New aromatic aldimines, isatine substituted ketimines based on (4,6-dichloro-1,3,5-triazin-2-yl)-hydrazine scaffold and polycyclic fused thiopyranothiazoles formed using hetero-Diels-Alder reactions starting from 4-thioxo-2-thiazolidinones and 5-norbornene-2,3-dicarboxylic acid triazino-derivatives synthetic approach is described. The application of condensation and cyclocondensation reactions of N-nucleophiles and carbonyl agents for synthesis a number of biologically active triazine derivatives is reported. Screening of anticancer activity in vitro yielded the most active compounds 3a, 8b, and 8f for different cell lines.
机译:新的芳族醛亚胺,基于(4,6-dichloro-1,3,5-triazin-2-yl)-肼骨架的isatine取代的酮亚胺和使用从4-thioxo-2开始的杂Diels-Alder反应形成的多环稠合噻吩并噻唑描述了噻唑烷酮和5-降冰片烯-2,3-二羧酸三嗪基衍生物的合成方法。据报道,N-亲核试剂和羰基试剂的缩合和环缩合反应用于合成许多具有生物活性的三嗪衍生物。体外抗癌活性的筛选产生了针对不同细胞系的活性最高的化合物3a,8b和8f。

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