Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Selective Derivatization of TPP on One Phenyl Ring by Nitration and Subsequent Nucleophilic Substitution of Hydrogen

  • Published : 20010100
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  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

Cited by

  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