Bulletin of the Korean Chemical Society

  • 제22권1호
  • /
  • Pages.9-10
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  • 2001
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Selective Derivatization of TPP on One Phenyl Ring by Nitration and Subsequent Nucleophilic Substitution of Hydrogen

  • 발행 : 20010100
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참고문헌

  1. Cancer Res v.38 Dougherty, T. J;Kaufman, J. E;Goldfarb, A
  2. Compr. Ther v.14 Delaney, T. F;Glatstein, E
  3. Otolaryngol Head Neck Surg v.102 Schweitzer, V. G
  4. Med. Biol. Environ. v.16 Milanesci, C;Biolo, R;Jori
  5. Photochem. Photobiol v.45 Kessel, D;Thompson, P;Saatio, K;Nantwi, K. D
  6. Photochem. Photobiol v.64 Pandey, R. K;Sumlin, A. B;Constantine, S;Aoudia, M;Potter, W. R;Bellnier, D. A;Hen-derson, B. W;Rogers, M. A;Smith, K. M;Dougherty, T. J
  7. Liebigs Ann./Recueil Makosza, M;Wojciechowski, K
  8. In Porphyrins and Metalloporphyrins Fuhrhop, J. H;Smith, K. M(ed.)
  9. J. Org. Chem. v.45 For typical procedure see Smith, K. M;Bisset, G. M. F;Bushell, M. J
  10. In The Porphyrins v.2 Fuhrhop, J. H;Dolphin, D(ed.)
  11. v.44 For bulky tertiary carbanion 5b because of its instability at higher temperature the t-BuOK/DMF system (-40°C)was used Mudryk, B;Makosza, M
  12. Zinc 5-(4-Nitrophenyl)-10,15,20-triphenylporphyrin was prepared quantitaively from 5-(-4-Nitrophenyl)-10,15,20-triphenylporphyrin as usual by using saturated methanol solution of zinc acetate dihydrate in methylene chloride with refluxing for an hour. The absorption bands in UV/Vis spectroscopy show a typical metalloporphyrins(λ = 587.8,548.2,419.0)
  13. J. Org. Chem v.54 Kruper Jr, W. J;Chamberlin, T. A;Kochanny, M

피인용 문헌

  1. ChemInform Abstract: Selective Derivatization of TPP on One Phenyl Ring by Nitration and Subsequent Nucleophilic Substitution of Hydrogen. vol.33, pp.14, 2001, https://doi.org/10.1002/chin.200214118
  2. Preparation of meso-Tetraarylporphyrins Nitrated in Two Neighboring Aromatic Rings vol.33, pp.23, 2001, https://doi.org/10.1081/scc-120026352
  3. Nucleophilic substitution of hydrogen in meso-nitroaryl-substituted porphyrins—unprotected at the NH-centers in the core ring vol.44, pp.23, 2001, https://doi.org/10.1016/s0040-4039(03)00933-x
  4. Selective Double Functionalization of meso-Tetraphenylporphyrin Complexes on the Same Pyrrole Unit by Tandem Electrophilic/Nucleophilic Aromatic Substitution vol.88, pp.5, 2001, https://doi.org/10.1002/hlca.200590091
  5. Frontiers in the electrophilic nitration ofmeso-tetraphenylporphyrin derivatives vol.5, pp.19, 2001, https://doi.org/10.1039/c8qo00571k
  6. Nitration of Porphyrin Systems: A Toolbox of Synthetic Methods vol.16, pp.4, 2001, https://doi.org/10.1002/asia.202000985