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Volumn 9, Issue 25, 2007, Pages 5291-5294

Multigram synthesis of a water-soluble porphyrazine and derived seco-porphyrazine labeling agents

Author keywords

[No Author keywords available]

Indexed keywords

METALLOPORPHYRIN; PHOTOSENSITIZING AGENT; WATER;

EID: 37349002456     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702481x     Document Type: Article
Times cited : (15)

References (45)
  • 1
    • 37349004984 scopus 로고    scopus 로고
    • For general literature on PDT, see: Dougherty, T. J.; Levy, J. G. In CRC Handbook of Organic Photochemistry and Photobiology, 2nd ed.; Horspool, W., Lend, F., Eds.; CRC Press: Boca Raton, FL, 2004; pp 147/117-147/141.
    • For general literature on PDT, see: Dougherty, T. J.; Levy, J. G. In CRC Handbook of Organic Photochemistry and Photobiology, 2nd ed.; Horspool, W., Lend, F., Eds.; CRC Press: Boca Raton, FL, 2004; pp 147/117-147/141.
  • 5
    • 0032936336 scopus 로고    scopus 로고
    • For general applications of optical agents on treatment of tumors, see: a
    • For general applications of optical agents on treatment of tumors, see: (a) Kessel, D.; Dougherty, T. J. Rev. Contemp. Pharmacother. 1999, 10, 19.
    • (1999) Rev. Contemp. Pharmacother , vol.10 , pp. 19
    • Kessel, D.1    Dougherty, T.J.2
  • 8
    • 37349001461 scopus 로고    scopus 로고
    • Jori, G. In CRC Handbook of Organic Photochemistry and Photobiology, 2nd ed.; Horspool, W., Lenci, F., Eds.; CRC Press: Boca Raton, FL, 2004; pp 146/110-146/141.
    • (d) Jori, G. In CRC Handbook of Organic Photochemistry and Photobiology, 2nd ed.; Horspool, W., Lenci, F., Eds.; CRC Press: Boca Raton, FL, 2004; pp 146/110-146/141.
  • 10
    • 0004214293 scopus 로고
    • Dolphin, D, Ed, Academic Press: New York, Vols
    • The Porphyrins; Dolphin, D., Ed.; Academic Press: New York, 1978-1979; Vols. 1-7.
    • (1978) The Porphyrins , vol.1-7
  • 11
    • 0003544982 scopus 로고
    • Leznoff, C. C, Lever, A. B. P, Eds, VCH Publishers: Weinheim, Germany, Vols
    • Phthalocyanines: Properties and Applications; Leznoff, C. C., Lever, A. B. P., Eds.; VCH Publishers: Weinheim, Germany, 1989-1996; Vols. 1-4.
    • (1989) Phthalocyanines: Properties and Applications , vol.1-4
  • 12
    • 0000817908 scopus 로고    scopus 로고
    • Peripherally-Functionalized Porphyrazines: Novel Metallomacrocycles with Broad, Untapped Potential
    • Karlin, K. D, Ed, J. Wiley and Sons: New York
    • (a) Michel, S. L. J.; Hoffman, B. M.; Baum, S. V.; Barrett, A. G. M. Peripherally-Functionalized Porphyrazines: Novel Metallomacrocycles with Broad, Untapped Potential. In Progress in Inorganic Chemistry; Karlin, K. D., Ed.; J. Wiley and Sons: New York, 2001; p 473.
    • (2001) Progress in Inorganic Chemistry , pp. 473
    • Michel, S.L.J.1    Hoffman, B.M.2    Baum, S.V.3    Barrett, A.G.M.4
  • 28
    • 0000326642 scopus 로고    scopus 로고
    • For the use of di-iminopyrrolines in the synthesis of unsymmetrical porphyrazines see: a
    • For the use of di-iminopyrrolines in the synthesis of unsymmetrical porphyrazines see: (a) Baumann, T. F.; Barrett, A. G. M.; Hoffman, B. M. Inorg. Chem. 1997, 36, 5661.
    • (1997) Inorg. Chem , vol.36 , pp. 5661
    • Baumann, T.F.1    Barrett, A.G.M.2    Hoffman, B.M.3
  • 41
    • 0027980842 scopus 로고    scopus 로고
    • For an example of the use of di-iminoisoindolines in the synthesis of unsymmetrical phthalocyanines see: Kobayashi, N, Higashi, Y, Osa, T. J. Chem. Soc, Chem. Commun. 1994, 1785
    • For an example of the use of di-iminoisoindolines in the synthesis of unsymmetrical phthalocyanines see: Kobayashi, N.; Higashi, Y.; Osa, T. J. Chem. Soc., Chem. Commun. 1994, 1785.
  • 42
    • 37349130041 scopus 로고    scopus 로고
    • It is possible that the macrocyclization reaction involves a sodium template and late transmetalation; see ref 10c
    • It is possible that the macrocyclization reaction involves a sodium template and late transmetalation; see ref 10c.
  • 43
    • 37349078107 scopus 로고    scopus 로고
    • 3BPz 15 was obtained in 72% yield when the reaction was performed with chromatographically purified 14.
    • 3BPz 15 was obtained in 72% yield when the reaction was performed with chromatographically purified 14.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.