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Aromatization of Hantzsch 1,4-Dihydropyridines with a Polymer-supported Hyervalent Iodine Reagent

  • Published : 2004.01.20

Abstract

Keywords

References

  1. In Comprehensive Medicinal Chemistry; Emmett,J. C., Volume Editor; Pergamon: Oxford, 1990; Vol. 3, Chapter14.1.
  2. Bocker, R. H.; Guengerich, F. P. J. Med. Chem. 1986, 29,1596. https://doi.org/10.1021/jm00159a007
  3. Guengerich, F. P.; Brian, W. R.; Iwasaki, M.; Sari,M.-A.; Baarnhielm, C.; Berntsson, P. J. Med. Chem. 1991, 34,1838. https://doi.org/10.1021/jm00110a012
  4. Lee, K.-H.; Ko, K.-Y. Bull. Korean Chem. Soc. 2002, 23, 1505 https://doi.org/10.5012/bkcs.2002.23.11.1505
  5. Ko, K.-Y.; Kim, J.-Y. Tetrahedron Lett.1999, 40, 3207. https://doi.org/10.1016/S0040-4039(99)00467-0
  6. Zolfigol, M. A.; Shirini, F.; Choghamarani, A. G.; Mohammadpoor-Baltork, I. Phosphorus Sulfur and Silicon and the RelatedElements 2003, 178, 1709. https://doi.org/10.1080/10426500307836
  7. Moriarty, R. M.; Vaid, R. K.; Koser, G. F. Synlett 1990, 365.
  8. Koser, G. F. Aldrichimica Acta 2001, 34, 89.
  9. Varvoglis, A. Tetrahedron 1997, 53, 1179. https://doi.org/10.1016/S0040-4020(96)00970-2
  10. Ley, S. V.; Thomas, A. W.; Finch, H. J. Chem. Soc., Perkin Trans.1 1999, 669.
  11. Sakuratani, K.; Togo, H. Synthesis 2003, 21.
  12. Togo, H.;Nogami, G.; Yokoyama, M. Synlett 1998, 534.
  13. Ficht, S.; Mülbaier, M.; Giannis, A. Tetrahedron 2001, 57, 4863. https://doi.org/10.1016/S0040-4020(01)00424-0
  14. Sorg, G.; Mengel, A.; Jung, G.; Rademann, J. Angew. Chem. Int.Ed. 2001, 40, 4395. https://doi.org/10.1002/1521-3773(20011203)40:23<4395::AID-ANIE4395>3.0.CO;2-R

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