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Original Articles

SYNTHESIS AND FUNGICIDAL ACTIVITIES OF DERIVATIVES OF 2-ALKYLTHIO-3-AMINO-4H-IMIDAZOL-4-ONE

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Pages 2287-2296 | Received 01 Feb 2004, Accepted 01 May 2004, Published online: 16 Aug 2010

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Hong-Xia Li, Yong Sun & Ming-Wu Ding. (2008) Reaction of Functionalized Carbodiimide with α-Amino Ester: A Selective Synthesis of 2,3,5-Trisubstituted Imidazol-4-ones. Synthetic Communications 38:24, pages 4328-4336.
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Articles from other publishers (7)

Ekaterina E. Vinogradova, Anna L. Alekseenko, Sergey V. Popkov, Natalya G. Kolotyrkina, Angelina N. Kravchenko & Galina A. Gazieva. (2023) Synthesis and Evaluation on the Fungicidal Activity of S-Alkyl Substituted Thioglycolurils. International Journal of Molecular Sciences 24:6, pages 5756.
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G. A. Gazieva, T. V. Nechaeva, N. N. Kostikova, N. V. Sigay, S. A. Serkov & S. V. Popkov. (2018) Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils. Russian Chemical Bulletin 67:6, pages 1059-1064.
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Galina A. Gazieva, Lada V. Anikina, Tatyana V. Nechaeva, Sergey A. Pukhov, Tatyana B. Karpova, Sergey V. Popkov, Yulia V. Nelyubina, Natalya G. Kolotyrkina & Angelina N. Kravchenko. (2017) Synthesis and biological evaluation of new substituted thioglycolurils, their analogues and derivatives. European Journal of Medicinal Chemistry 140, pages 141-154.
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S. G. Bubbly, S. B. Gudennavar, N. M. Nanje Gowda, Rita Bhattacharjee, V. Gayathri & S. Natarajan. (2011) Synthesis, Characterization and Biological Activity Studies on 6-p-Dimethylaminophenyl-5,6-dihydrobenzoimidazo[1,2-c]quinazoline: Crystal Structure of the Title Compound and Comparative Study with Related Derivatives. Journal of Chemical Crystallography 42:4, pages 305-312.
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Yanggen Hu, Min Liu & Mingwu Ding. (2010) Efficient Synthesis of New Tetracyclic Benzofuro[3,2‐ d ]‐imidazo[1,2‐ a ]pyrimidine‐2,5‐(1 H ,3 H )‐diones . Chinese Journal of Chemistry 28:2, pages 309-312.
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Ming‐Wu Ding, Yun‐Feng Chen & Nian‐Yu Huang. (2005) Synthesis and Fungicidal Activities of Derivatives of 2‐Alkylthio‐3‐amino‐4H‐imidazol‐4‐one.. ChemInform 36:13.
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