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Volumn 67, Issue 1, 2006, Pages 255-267

A new synthesis of acenaphthobenzoporphyrin and fluoranthobenzoporphyrin

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EID: 33747141083     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-05-S(T)23     Document Type: Article
Times cited : (43)

References (38)
  • 4
    • 0003641908 scopus 로고    scopus 로고
    • Kadish K.M., Smith K.M., and Guilard R. (Eds), Academic Press
    • In: Kadish K.M., Smith K.M., and Guilard R. (Eds). The Porphyrin Handbook Vol. 1-20 (2001), Academic Press
    • (2001) The Porphyrin Handbook , vol.1-20
  • 5
    • 0004146858 scopus 로고    scopus 로고
    • Archer M.D., and Hill R. (Eds), Imperial College Press, San Diego
    • In: Archer M.D., and Hill R. (Eds). Clean Electricity from Photovoltaics (2001), Imperial College Press, San Diego
    • (2001) Clean Electricity from Photovoltaics
  • 6
    • 0038010936 scopus 로고    scopus 로고
    • Porphyrins and phthalocyanine have been used as sensitizers for solar cell, see
    • Gratzel M. Prog. Photovoltaics 8 (2000) 171 Porphyrins and phthalocyanine have been used as sensitizers for solar cell, see
    • (2000) Prog. Photovoltaics , vol.8 , pp. 171
    • Gratzel, M.1
  • 24
    • 0025016417 scopus 로고
    • where nitroalkenes are converted into pyrroles. Aromatic nitro compounds are used instead of nitroalkenes for the preparation of pyrroles with fused aromatics, see
    • where nitroalkenes are converted into pyrroles. Aromatic nitro compounds are used instead of nitroalkenes for the preparation of pyrroles with fused aromatics, see. Barton D.H.R., Kervagoret J., and Zard S.Z. Tetrahedron 46 (1990) 7587
    • (1990) Tetrahedron , vol.46 , pp. 7587
    • Barton, D.H.R.1    Kervagoret, J.2    Zard, S.Z.3
  • 28
    • 0033978398 scopus 로고    scopus 로고
    • However, nitrobenzene failed to react at all to give the related isoindoles. Very recently, this difficulty was overcome by the oxidation of cyclohexane fused porphyrins, see
    • However, nitrobenzene failed to react at all to give the related isoindoles. Very recently, this difficulty was overcome by the oxidation of cyclohexane fused porphyrins, see. Lash T.D., Thompson M.L., Werner T.M., and Spence J.D. Synlett (2000) 213
    • (2000) Synlett , pp. 213
    • Lash, T.D.1    Thompson, M.L.2    Werner, T.M.3    Spence, J.D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.