Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Concise Synthesis of Pelanserine, Goshuyuamide II, and Wuchuyuamide II with Quinazolinedione Nuclei

  • Li, Xin (School of Chemical Engineering and Technology, Yeungnam University) ;
  • Lee, Yong-Rok (School of Chemical Engineering and Technology, Yeungnam University) ;
  • Kim, Sung-Hong (Analysis Research Division, Daegu Center, Korea Basic Science Institute)
  • Received : 2011.06.17
  • Accepted : 2011.07.15
  • Published : 2011.09.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Undheim, K.; Benneche, T. In Comprehensive Heterocyclic Chemistry II; Katritzky, A. R.; Rees, C. W.; Scriven, E. F. V., Eds.; Elsevier: Oxford, UK, 1996; Vol. 6, p 93.
  2. Ismail, M. A. H.; Barker, S.; El Ella, D. A. A.; Abouzid, K. A. M.; Toubar, R. A.; Todd, M. H. J. Med. Chem. 2006, 49, 1526. https://doi.org/10.1021/jm050232e
  3. Goto, S.; Tsuboi, H.; Kagara, K. Chem. Express 1993, 8, 761.
  4. Liu, J.; Birzin, E. T.; Chan, W.; Yang, Y. T.; Lee, Y. P.; DaSilva, C.; Hayes, E. C.; Mosley, R. T.; DiNinno, F.; Rohrer, S. P.; Schaeffer, J. M.; Hammond, M. L. Buckley, G. M.; Davies, N.; Dyke, H. J.; Gilbert, P. J.; Hannah, D. R.; Haughan, A. F.; Hunt, C. A.; Pitt, W. R.; Profit, R. H.; Ray, N. C.; Richard, M. D.; Sharpe, A.; Taylor, A. J.; Whitworth, J. M.; Williams, S. C. Bioorg. Med. Chem. Lett. 2005, 15, 751. https://doi.org/10.1016/j.bmcl.2004.11.015
  5. Hayao, S.; Havera, H. J.; Strycker, W. G.; Leipzig, T. J.; Kulp, R. A.; Hartzler, H. E. J. Med. Chem. 1965, 8, 807. https://doi.org/10.1021/jm00330a017
  6. Leysen, J. E.; Niemegeers, C. E.; Van Nueten, J. M.; Lauduron, P. M. Mol. Pharmacol. 1982, 21, 301.
  7. Darchen, F.; Scherman, D.; Laduron, P. M.; Henry, J. P. Mol. Pharmacol. 1988, 33, 672.
  8. Jin, H.-Z.; Du, J.-L.; Zhang, W.-D.; Chen, H.-S.; Lee, J.-H.; Lee, J.-J. J. Asian Nat. Prod. Res. 2007, 9, 685. https://doi.org/10.1080/10286020601103296
  9. Shoji, N.; Umeyama, A.; Iuchi, A.; Saito, N.; Arihara, S. J. Nat. Prod. 1989, 52, 1160. https://doi.org/10.1021/np50065a043
  10. Zuo, G. Y.; Yang, X. S.; Hao, X. J. Chinese Chem. Lett. 2000, 11, 127.
  11. Encyclopedia of Chinese Mediciene, People's Press, Shanghai, 1977, p 1118.
  12. Garcia, J. D.; Somanathan, R.; Rivero, I. A.; Aguirre, G.; Hellberg, L. H. Synth. Commun. 2000, 30, 2707. https://doi.org/10.1080/00397910008086895
  13. Bergman, J.; Bergman, S. J. Org. Chem. 1985, 50, 1246. https://doi.org/10.1021/jo00208a018
  14. Li, X.; Lee, Y. R. Bull. Korean Chem. Soc. 2011, 32, 2121. https://doi.org/10.5012/bkcs.2011.32.6.2121
  15. Cortez, R.; Rivero, I. A.; Somanathan, R.; Aguirre, G.; Ramirez, F. Synth. Commun. 1991, 21, 285. https://doi.org/10.1080/00397919108020823
  16. Szab-Pusztay, K.; Szab, L. Synthesis 1979, 276.

Cited by

  1. ChemInform Abstract: Concise Synthesis of Pelanserine (IIIa), Goshuyuamide II (VII), and Wuchuyuamide II (VIII) with Quinazolinedione Nuclei. vol.43, pp.10, 2012, https://doi.org/10.1002/chin.201210211
  2. )-dione vol.70, pp.8, 2014, https://doi.org/10.1107/S160053681401602X
  3. Utilization of isatoic anhydride in the syntheses of various types of quinazoline and quinazolinone derivatives vol.46, pp.12, 2016, https://doi.org/10.1080/00397911.2016.1177087
  4. Iridium-Catalyzed C-H Amination of Weinreb Amides: A Facile Pathway toward Anilines and Quinazolin-2,4-diones vol.85, pp.20, 2020, https://doi.org/10.1021/acs.joc.0c01789