Bulletin of the Korean Chemical Society

  • 제23권12호
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  • Pages.1699-1701
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  • 2002
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Studies on Synthesis and Biological Activites of Novel Triazole Compounds Containing N,N-Diakyldithiocarbamate

  • 발행 : 2002.12.20
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참고문헌

  1. Shi, Y.-N.; Lu, Y.-C.; Fang, J.-X. Chemical J. Chinese Universities 1995, 16(11), 1710-1713.
  2. Elbe, H. L.; Buechel, K. H.; Luerssen, K. et al. Ger Offen. 3 144 670, 1983.
  3. Anderson, N. H. Proceeding of 5th International Congress of Pesticide Chemistry (IUPAC); Kyoto, Japan 1982; p 345.
  4. Shi, Y.-N.; Xu, L.-Z.; Fang, J.-X. Chemical J. Chinese Universities 1991, 9(12), 1190-1193.
  5. Gracia Albert, J. U.S. Patent, 2 229 562, 1941.
  6. Hill, G. H.; Kropa, L. E. J. Am. Chem. Soc. 1953, 55, 2509.
  7. Holmwood, G.; Oeckl, S.; Stetter, J. Ger. Offen. 2 937 595, 1981.

피인용 문헌

  1. Synthesis and Biological Activities of Novel Triazole Compounds Containing 1,3-Dioxolane Rings vol.9, pp.11, 2004, https://doi.org/10.3390/91100913
  2. In vitro Antibacterial Activity of Dithiocarbamate Organotin(IV) Complexes Towards Staphylococcus aureus vol.31, pp.1-2, 2008, https://doi.org/10.1515/MGMC.2008.31.1-2.21
  3. A simple and efficient synthesis and dynamic NMR studies of some new podands of dithiocarbamates formed from bis(naphthyl) derivatives vol.22, pp.5, 2011, https://doi.org/10.1002/hc.20730
  4. Comparative studies on carbon paste electrodes based on three dithiocarbamate podands as ionophore in Ag(i) sensors vol.4, pp.3, 2012, https://doi.org/10.1039/c2ay05559g
  5. New carbodithioate derivatives: synthesis, characterization, and in vitro antibacterial, antifungal, antitubercular, and antimalarial activity vol.22, pp.10, 2013, https://doi.org/10.1007/s00044-013-0472-0
  6. Synthesis, docking and preliminary in vivo evaluation of serotonin dithiocarbamate as novel SPECT neuroimaging agent vol.4, pp.6, 2013, https://doi.org/10.1039/c3md00044c
  7. Synthesis and Dynamic NMR Studies of Some New Symmetrical Podands of Dithiocarbamates Formed from Bis(N-thiazol)chloroacetamides vol.50, pp.2, 2013, https://doi.org/10.1002/jhet.915
  8. A novel dithiocarbamate derivative induces cell apoptosis through p53-dependent intrinsic pathway and suppresses the expression of the E6 oncogene of human papillomavirus 18 in HeLa cells vol.20, pp.6, 2015, https://doi.org/10.1007/s10495-015-1114-4
  9. Synthesis of new triazolyl-N,N-Dialkyldithiocarbamates as antifungal agents vol.28, pp.11, 2005, https://doi.org/10.1007/BF02978200
  10. Synthesis, structure and biological activities of [α-(alkylcarbonyl)-2-(1,2,4-triazol-1-yl)]ethyl-N,N-dialkydithiocarbamate derivatives vol.43, pp.4, 2006, https://doi.org/10.1002/jhet.5570430417
  11. Syntheses and biological activities of novel triazole compounds vol.44, pp.1, 2007, https://doi.org/10.1002/jhet.5570440112
  12. )-thione vol.64, pp.6, 2008, https://doi.org/10.1107/S1600536808014967
  13. Deamination of Some N-Amino Nitrogen Heterocycles Using Preyssler’s Anion vol.139, pp.2, 2008, https://doi.org/10.1007/s00706-007-0715-1
  14. Synthesis, Structure and Biological Activities of S-[a-(4-Methoxyphenylcarbonyl)-2-(1, 2, 4-triazole-1-yl)] ethyl-N, N-dimethyldithiocarbamate vol.21, pp.12, 2002, https://doi.org/10.1002/cjoc.20030211218
  15. Studies on Synthesis and Biological Activities of Novel Triazole Compounds Containing N,N-Dialkyldithiocarbamate. vol.34, pp.17, 2002, https://doi.org/10.1002/chin.200317110
  16. Synthesis, structure and biological activities of novel triazole compounds containing N,N-dialkyldithiocarbamate moiety vol.22, pp.7, 2002, https://doi.org/10.1002/cjoc.20040220717
  17. Synthesis, structure and biological activities of novel triazole compounds containing 4,6-dimethyl-pyrimidin-2-ylthio group vol.22, pp.11, 2004, https://doi.org/10.1002/cjoc.20040221119
  18. Study on Structure and Biological Activities of Novel Triazole Compounds Containing 1,3-Dithiolane Ring vol.23, pp.10, 2002, https://doi.org/10.1002/cjoc.200591421
  19. Synthesis and Crystal Structure of N′-(4-fluorobenzylidene)- 2-(1H-1,2,4-triazole-1-yl) acetohydrazide vol.22, pp.5, 2002, https://doi.org/10.1016/s1005-9040(06)60164-5
  20. A Simple and Eco-Compatible One-Pot Synthesis of New Symmetrical Dithiocarbamate Podands and Their Dynamic NMR Studies vol.188, pp.9, 2013, https://doi.org/10.1080/10426507.2012.717133