Bulletin of the Korean Chemical Society

  • 제34권4호
  • /
  • Pages.1290-1292
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  • 2013
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Alkaloids from Papaver setigerum

  • Lee, Chul (College of Pharmacy, Chungbuk National University) ;
  • Choe, Sanggil (Forensic Chemistry Division, Southern District Office, National Forensic Service) ;
  • Lee, Jin Woo (College of Pharmacy, Chungbuk National University) ;
  • Jin, Qinghao (College of Pharmacy, Chungbuk National University) ;
  • Lee, Mi Kyeong (College of Pharmacy, Chungbuk National University) ;
  • Hwang, Bang Yeon (College of Pharmacy, Chungbuk National University)
  • 투고 : 2013.01.03
  • 심사 : 2013.01.24
  • 발행 : 2013.04.20
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참고문헌

  1. Kadereit, J. W. Papaveraceae; Kubitzki, K.; Rohweer, J. G.; Bittrich, V., Ed.; The Families and Genera of Vascular Plants; Springer-Verlag: Berlin, Heidelberg, Germany, 1993; Vol. 2, p 20.
  2. Preininger, V. Chemotaxonomy of Papaveraceae and Fumariaceae; Brossi, A., Ed.; The alkaloids; Academic Press: London, U. S.A., 1986; p 2.
  3. Preininger, V.; Novak, J.; Santavy, F. Planta Med. 1981, 41, 119. https://doi.org/10.1055/s-2007-971687
  4. Frick, S.; Kramell, R.; Schmidt, J.; Fist, A. J.; Kutchan, T. M. J. Nat. Prod. 2005, 68, 666. https://doi.org/10.1021/np0496643
  5. Choe, S.; Lee, E.; Jin, G.; Lee, Y. H.; Kim, S. Y.; Choi, H.; Chung, H.; Hwang, B. Y.; Kim, S. Forensic Sci. Int. 2012, 222, 387. https://doi.org/10.1016/j.forsciint.2012.08.002
  6. Choe, S.; Kim, S.; Lee, C.; Yang, W.; Park, Y.; Choi, H.; Chung, H.; Lee, D.; Hwang, B. Y. Forensic Sci. Int. 2011, 211, 51. https://doi.org/10.1016/j.forsciint.2011.04.015
  7. Slavík, J.; Slavíkova, L. Collect. Czech. Chem. Commun. 1996, 61, 1047. https://doi.org/10.1135/cccc19961047
  8. Gilmore, C. D.; Allan, K. M.; Stoltz, B. M. J. Am. Chem. Soc. 2008, 130, 1558. https://doi.org/10.1021/ja0780582
  9. Janssen, R. H. A. M.; Wijkens, P.; Kruk, C.; Biessels, H. W. A.; Menichini, F.; Theuns, H. G. Phytochemistry 1990, 29, 3331. https://doi.org/10.1016/0031-9422(90)80210-8
  10. Marsaioli, A. J.; Magalhães, A. F.; Rúveda, E. A.; Reis, F. d. A. M. Phytochemistry 1980, 19, 995. https://doi.org/10.1016/0031-9422(80)85165-X
  11. Zhang, G.; Rucker, G.; Breitmaier, E.; Nieger, M.; Mayer, R.; Steinbeck, C. Phytochemistry 1995, 40, 299. https://doi.org/10.1016/0031-9422(95)00192-A

피인용 문헌

  1. Isoxazolidine: A Privileged Scaffold for Organic and Medicinal Chemistry vol.116, pp.24, 2016, https://doi.org/10.1021/acs.chemrev.6b00543
  2. Synthesis of Chromenoisoxazolidines from Substituted Salicylic Nitrones via Visible-Light Photocatalysis vol.21, pp.5, 2013, https://doi.org/10.1021/acs.orglett.9b00097
  3. Synthesis of 2′,3′,4′-triaryl-5,6-dihydro-8H-spiro[indolizine-7,5′-isoxazolidin]-8-ones via 1,3-dipolar cycloaddition reaction involving (Z)-C-aryl-N-phenylnitrones vol.56, pp.8, 2020, https://doi.org/10.1007/s10593-020-02774-6
  4. Synthesis of (±)‐Setigerumine I: Biosynthetic Origins of the Elusive Racemic Papaveraceae Isoxazolidine Alkaloids** vol.133, pp.52, 2013, https://doi.org/10.1002/ange.202111049
  5. Synthesis of (±)‐Setigerumine I: Biosynthetic Origins of the Elusive Racemic Papaveraceae Isoxazolidine Alkaloids** vol.60, pp.52, 2013, https://doi.org/10.1002/anie.202111049