Collection of Czechoslovak Chemical Communications - digital archive 

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• Li Tangle, Hu Dandan, Huang Yiwen, Zhou Yu, Zhang Jun-Qi, Zhang Chun, Zhang Yili, Hou Yanan, Ren Hongjun: Light-Driven Access to Selenium-Substituted Thiazole-2-imine Derivatives. J. Org. Chem. 2024. <https://doi.org/10.1021/acs.joc.3c02698>
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• Mohr Eduarda Talita Bramorski, Lubschinski Tainá Larissa, da Rosa Julia Salvan, Vieira Guilherme Nicácio, Felisberto Mariano, Romualdo Robson Ruan, Ferreira Misael, Sá Marcus Mandolesi, Dalmarco Eduardo Monguilhott: The anti-inflammatory activity of 2-iminothiazolidines: evidence for macrophage repolarization. Inflammopharmacol 2022, 30, 2427. <https://doi.org/10.1007/s10787-022-01084-x>
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• Yahyazadeh Asieh, Abbasi Shiran Jafar, M. Yamin Bohari, Shirini Farhad, Mamaghani Manouchehr: One-Pot, Three Component Synthesis of Thiazol-2(3H)-imines Using Poly(4-vinylpyridine) as an Efficient Reusable Heterogeneous Basic Catalyst. HETEROCYCLES 2015, 91, 113. <https://doi.org/10.3987/COM-14-13122>
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• Saeed Aamer, Al‐Masoudi Najim A., Latif Muhammad: Synthesis and Antiviral Activity of New Substituted Methyl [2‐(arylmethylene‐hydrazino)‐4‐oxo‐thiazolidin‐5‐ylidene]acetates. Archiv der Pharmazie 2013, 346, 618. <https://doi.org/10.1002/ardp.201300057>
• Saeed Sohail, Hussain Rizwan, Ali Muhammad: Synthesis and Antimicrobial Activity of N‐[(2Z)‐3‐(4,6‐Substitutedpyrimidin‐2‐yl)‐4‐phenyl‐1,3‐thiazol‐2(3H)‐ylidene]‐3, 5‐dinitrobenzamide Analogues. Journal of Heterocyclic Chem 2013, 50, 237. <https://doi.org/10.1002/jhet.964>
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