대한화학회지 (Journal of the Korean Chemical Society)

  • 제60권6호
  • /
  • Pages.457-461
  • /
  • 2016
  • /
  • 1017-2548(pISSN)
  • /
  • 2234-8530(eISSN)
대한화학회 (Korean Chemical Society)
권호 표지
DOI QR코드

DOI QR Code

An Efficient Synthesis of N,N-Dialkyl-5-(chlorophenyl)-2-furancarbothioamides from 2-Furoic Acid

  • Lee, Hee Ju (Department of Chemistry, College of Natural Science, Duksung Women's University) ;
  • Lee, Jae In (Department of Chemistry, College of Natural Science, Duksung Women's University)
  • 투고 : 2016.08.09
  • 심사 : 2016.09.13
  • 발행 : 2016.12.20
PDF 다운로드
⟨ 이전 논문 다음 논문 ⟩

초록

키워드

참고문헌

  1. Devillanova, F. A. Handbook of Chalcogen Chemistry; RSC Publishing: Cambridge, U. K., 2007; p 145.
  2. (a) Xu, Y.; Xue, S. Chem. Res. Chin. Univ. 2009, 25, 846.
  3. (b) Cui, Z.-N.; Li, Y.-S.; Hu, D.-K.; Tian, H.; Jiang, J.-N.; Wang, Y.; Yan, X.-J. Sci. Rep. 2016, 6, doi: 10.1038.
  4. (a) Kim, T.-H.; Hauser, F.; Ha, T.; Xue, S.; Bohmer, M.; Nishimura, N.; Munemasa, S.; Hubbard, K.; Peine, N.; Lee, B.; Lee, S.; Robert, N.; Parker, J. E.; Schroeder, J. I. Current Biol. 2011, 21, 990. https://doi.org/10.1016/j.cub.2011.04.045
  5. (b) Kim, T.-H.; Kunz, H.-H.; Bhattacharjee, S.; Hauser, F.; Park, J.; Engineer, C.; Liu, A.; Ha, T.; Parker, J. E.; Gassmann, W.; Schroeder, J. I. Plant Cell 2012, 24, 5177. https://doi.org/10.1105/tpc.112.107235
  6. (c) Rigal, A.; Ma, Q.; Robert, S. Frontiers Plant Sci. 2014, 5, 1.
  7. (a) Ristova, D.; Busch, W. Plant Physiol. 2014, 166, 518. https://doi.org/10.1104/pp.114.244749
  8. (b) Kunz, H.-H.; Park, J.; Mevers, E.; Garcia, A. V.; Highhouse, S.; Gerwick, W. H.; Parker, J. E.; Schroeder, J. I. Plos One 2016, 11, 1.
  9. (a) Janda, L.; Voticky, Z. Chem. Zvesti 1984, 38, 507.
  10. (b) Hari, D. P.; Konig, B. Angew. Chem. Int. Ed. 2013, 52, 4734. https://doi.org/10.1002/anie.201210276
  11. (a) Cui, Z.-N.; Wang, Z.; Li, Y.; Zhou, X.-Y.; Ling, Y.; Yang, X.-L. Chin. J. Org. Chem. 2007, 27, 1300.
  12. (b) Cui, Z.; Zhang, L.; Huang, J.; Yang, X.; Ling, Y. Chin. J. Chem. 2010, 28, 1257. https://doi.org/10.1002/cjoc.201090218
  13. (a) Bai, L. Chin. Chem. Lett. 2009, 20, 158. https://doi.org/10.1016/j.cclet.2008.10.050
  14. (b) Zhou, W.-J.; Wang, K.-H.; Wang, J.-X.; Gao, Z.-R. Tetrahedron 2010, 66, 7633. https://doi.org/10.1016/j.tet.2010.07.022
  15. (a) Cui, Z.-N.; Huang, J.; Li, Y.; Ling, Y.; Yang, X.-L.; Chen, F.-H. Chin. J. Chem. 2008, 26, 916. https://doi.org/10.1002/cjoc.200890168
  16. (b) Cui, Z.; Li, X.; Tian, F.; Yan, X. Int. J. Mol. Sci. 2014, 15, 8941. https://doi.org/10.3390/ijms15058941
  17. Li, Z.; Wang, X. Synth. Comm. 2002, 32, 3357. https://doi.org/10.1081/SCC-120014043
  18. Guerrero, M.; Urbano, M.; Velaparthi, S.; Zhao, J.; Schaeffer, M. T.; Brown, S.; Rosen, H.; Roberts, E. Bioorg. Med. Chem. Lett. 2011, 21, 3632. https://doi.org/10.1016/j.bmcl.2011.04.097
  19. (a) Curphey, T. J. J. Org. Chem. 2002, 67, 6461. https://doi.org/10.1021/jo0256742
  20. (b) Ozturk, T.; Ertas, E.; Mert, O. Chem. Rev. 2007, 107, 5210. https://doi.org/10.1021/cr040650b
  21. Kim, S.; Lee, J. I.; Ko, Y. K. Tetrahedron Lett. 1984, 25, 4943. https://doi.org/10.1016/S0040-4039(01)91265-1
  22. (a) Berry, D. J.; DiGiovanna, C. V.; Metrick, S. S.; Murugan, R. Arkivoc 2001, 201.
  23. (b) Xu, S.; Held, I.; Kempf, B.; Mayr, H.; Steglich, W.; Zipse, H. Chem. Eur. J. 2005, 11, 4751. https://doi.org/10.1002/chem.200500398
  24. (c) Hong, H. J.; Lee, J. I. J. Kor. Chem. Soc. 2014, 58, 569. https://doi.org/10.5012/jkcs.2014.58.6.569
  25. Przychodzen, W. Eur. J. Org. Chem. 2005, 2002.

피인용 문헌

  1. Convenient Synthesis of Aryl-Substituted (Hetero)arylcarbothioamides from Bromo(hetero)arylcarboxylic Acids vol.61, pp.5, 2016, https://doi.org/10.5012/jkcs.2017.61.5.286