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首页> 外文期刊>Journal of sulfur chemistry >Synthesis of some new 5-substituted-3-phenyl-4-thioxo-2-thiazolidinones and their fused thiopyrano[2,3-d]thiazole derivatives
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Synthesis of some new 5-substituted-3-phenyl-4-thioxo-2-thiazolidinones and their fused thiopyrano[2,3-d]thiazole derivatives

机译:一些新的5-取代的-3-苯基-4-硫代氧-2-噻唑烷酮及其稠合的硫代吡喃并[2,3-d]噻唑衍生物的合成

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摘要

The new 5-arylmethylene-3-phenyl-4-thioxo-2-thiazolidinone derivatives have been synthesized by condensation of -(4-formylphenoxy)acetophenone derivatives with 3-phenyl-4-thioxo-2-thiazolidinone, in good yields. The cycloaddition of the newly synthesized compounds to N-arylmaleimides, ethyl acrylate and -nitrostyrene has been studied. Under thermal reaction conditions [4+2] cycloaddition proceeds with complete site- and regioselectivity to yield the new fused thiopyrano[2,3-d]thiazole derivatives.
机译:新的5-芳基亚甲基-3-苯基-4-硫代-2-噻唑烷酮衍生物是通过-(4-甲酰基苯氧基)苯乙酮衍生物与3-苯基-4-硫代-2-噻唑烷酮的缩合反应合成的。已经研究了新合成的化合物与N-芳基马来酰亚胺,丙烯酸乙酯和-硝基苯乙烯的环加成反应。在热反应条件下[4 + 2],环加成反应以完全的位点和区域选择性进行,以生成新的稠合噻吩并[2,3-d]噻唑衍生物。

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