메뉴 건너뛰기




Volumn 35, Issue 7, 2005, Pages 929-934

Efficient and versatile single-pot alternative approach to dipyrromethanes

Author keywords

5,10 Tripyrranes; Carbonyl equivalents; Dipyrromethanes; Oxazinanes; Tetra meso arylporphyrins

Indexed keywords

5,10 TRIPYRRANE; CARBENE; DIPYRROMETHANE DERIVATIVE; METHANE; PORPHYRIN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 16644366113     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-200051691     Document Type: Article
Times cited : (9)

References (18)
  • 1
    • 0035438419 scopus 로고    scopus 로고
    • Review article: Synthetic routes to multiporphyrin arrays
    • and references cited therein.
    • Burrell, A. K.; Officer, D. L.; Plieger, P. G.; Reid, D. C. W. Review article: synthetic routes to multiporphyrin arrays. Chem. Rev. 2001, 2751 and references cited therein.
    • (2001) Chem. Rev. , pp. 2751
    • Burrell, A.K.1    Officer, D.L.2    Plieger, P.G.3    Reid, D.C.W.4
  • 2
    • 0032560210 scopus 로고    scopus 로고
    • Porphyrin-based photosensitizers for use in photodynamic therapy
    • Sternberg, E. D.; Dolphin, D. Porphyrin-based photosensitizers for use in photodynamic therapy. Tetrahedron 1998, 54, 4151.
    • (1998) Tetrahedron , vol.54 , pp. 4151
    • Sternberg, E.D.1    Dolphin, D.2
  • 3
    • 0004214293 scopus 로고
    • Academic Press: New York
    • The Porphyrins; Dolphin, D., Ed., Academic Press: New York, 1978/1979; Vols. 1-7.
    • (1978) The Porphyrins , vol.1-7
    • Dolphin, D.1
  • 5
    • 0000254084 scopus 로고    scopus 로고
    • Remarkable effects of metal, solvent, and oxidant on metalloporphyrin- catalyzed enantioselective epoxidation of olefins
    • Gross, Z.; Ini, S. Remarkable effects of metal, solvent, and oxidant on metalloporphyrin-catalyzed enantioselective epoxidation of olefins. J. Org. Chem. 1997, 62, 5514.
    • (1997) J. Org. Chem. , vol.62 , pp. 5514
    • Gross, Z.1    Ini, S.2
  • 7
    • 0029860699 scopus 로고    scopus 로고
    • Soluble synthetic multiporphyrin arrays, 1: Modular design and synthesis
    • Wagner, R. W.; Johnson, T. E.; Lindsey, J. S. Soluble synthetic multiporphyrin arrays, 1: modular design and synthesis. J. Am. Chem. Soc. 1996, 118, 11166.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 11166
    • Wagner, R.W.1    Johnson, T.E.2    Lindsey, J.S.3
  • 8
    • 0037128481 scopus 로고    scopus 로고
    • A new synthetic route to donor-acceptor porphyrins
    • (a) Plater, M. J.; Aiken, S.; Bourhill, G. A new synthetic route to donor-acceptor porphyrins. Tetrahedron 2002, 58, 2405;
    • (2002) Tetrahedron , vol.58 , pp. 2405
    • Plater, M.J.1    Aiken, S.2    Bourhill, G.3
  • 9
    • 0025694679 scopus 로고
    • Synthesis and characterization of quinone-substituted octaalkyl porphyrin monomers and dimmers
    • (b) Sessler, J. L.; Johnson, M. R.; Creager, S. E.; Fettinger, J. C.; Ibers, J. A. Synthesis and characterization of quinone-substituted octaalkyl porphyrin monomers and dimmers. J. Am. Chem. Soc. 1990, 772, 9310;
    • (1990) J. Am. Chem. Soc. , vol.772 , pp. 9310
    • Sessler, J.L.1    Johnson, M.R.2    Creager, S.E.3    Fettinger, J.C.4    Ibers, J.A.5
  • 10
    • 0025630490 scopus 로고
    • Stepwise syntheses of unsymmetrical tetra-arylporphyrins: Adaptation of the Macdonald dipyrrole self-condensation methodology
    • (c) Wallace, D. M.; Smith, K. M. Stepwise syntheses of unsymmetrical tetra-arylporphyrins: adaptation of the Macdonald dipyrrole self-condensation methodology. Tetrahedron Lett. 1990, 31, 7265;
    • (1990) Tetrahedron Lett. , vol.31 , pp. 7265
    • Wallace, D.M.1    Smith, K.M.2
  • 12
  • 13
    • 0034602310 scopus 로고    scopus 로고
    • Rational syntheses of porphyrins bearing up to four different meso substituents
    • (f) Dharma Rao, P.; Dhanalekshmi, S.; Littler, B. L.; Lindsey, J. S. Rational syntheses of porphyrins bearing up to four different meso substituents. J. Org. Chem. 2000, 65, 7323.
    • (2000) J. Org. Chem. , vol.65 , pp. 7323
    • Dharma Rao, P.1    Dhanalekshmi, S.2    Littler, B.L.3    Lindsey, J.S.4
  • 15
    • 0035840111 scopus 로고    scopus 로고
    • Modified Pictet-Spengler reaction: A highly diastereoselective approach to 1,2,3-trisubstituted-1,2,3,4-tetrahydro-β-carbolines using perhydro-1,3-heterocycles
    • and references cited therein
    • Singh, K.; Deb, P. K.; Venugopalan, P. Modified Pictet-Spengler reaction: a highly diastereoselective approach to 1,2,3-trisubstituted-1,2,3,4- tetrahydro-β-carbolines using perhydro-1,3-heterocycles. Tetrahedron 2001, 57, 7939 and references cited therein.
    • (2001) Tetrahedron , vol.57 , pp. 7939
    • Singh, K.1    Deb, P.K.2    Venugopalan, P.3
  • 17
    • 2742541897 scopus 로고
    • Carbon transfer reactions with heterocycles, Part 7: A facile synthesis of unsymmetrically substituted 1,4-dihydropyridines
    • Singh, H.; Singh, K.; Kaur, P.; Sarin, P. Carbon transfer reactions with heterocycles, Part 7: a facile synthesis of unsymmetrically substituted 1,4-dihydropyridines. J. Chem. Res., Synop. 1993, 120.
    • (1993) J. Chem. Res., Synop. , pp. 120
    • Singh, H.1    Singh, K.2    Kaur, P.3    Sarin, P.4
  • 18
    • 0038180395 scopus 로고    scopus 로고
    • Parallel synthesis of unsymmetrically substituted tetraphenyl porphyrins on Wang resin
    • Shi, B.; Scobie, M.; Boyle, R. W. Parallel synthesis of unsymmetrically substituted tetraphenyl porphyrins on Wang resin. Tetrahedron Lett. 2003, 44, 5083.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 5083
    • Shi, B.1    Scobie, M.2    Boyle, R.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.