5,10,15,20-Tetrakis(2,6-dihydroxyphenyl)-21H,23H-porphine

Inorganic Syntheses

Volumn 31, Issue , 1997, Pages 117-122

  Collman, James P ^a   Lee, Virgil J ^a   Zhang, Xumu ^a   Yuan, Hong Ping ^b   Woo, L Keith ^b  

^a STANFORD UNIVERSITY   (United States)

^b IOWA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PORPHINE;

EID: 0006122997     PISSN: 00738077     EISSN: None     Source Type: Book Series    
DOI: None     Document Type: Article

References (20)

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3. J. P. Collman, Acc. Chem. Res., 10, 265 (1977).
4. For examples of porphyrin-catalyzed regioselective oxidations see (a) B. R. Cook, T. J. Reinert, and K. S. Suslick, J. Am. Chem. Soc., 108, 7281 (1986)
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8. For a review of biomimetic systems that are derived from 5,10,15,20-tetrakis(2-aminophenyl)-21H,23H-porphine see (a) B. Morgan and D. Dolphin, Structure and Bonding, 64, 115 (1987).
9. For biomimetic systems that are derived from 5,10,15,20-tetrakis(2,6- diaminophenyl)-21H,23H-porphine see (b) C. A. Quintana, R. A. Assink, and J. A. Shelnutt, Inorg. Chem., 28, 3421 (1989)
10. and (c) C. M. Drain and B. B. Corden, Inorg. Chem., 28, 4374 (1989).
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14. Available from Aldrich Chemical Company, Inc.
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19. Tsuchida et al. have prepared 3 from 1 in 9.3% overall yield by a different procedure. See E. Tsuchida, T. Komatsu, E. Hasegawa, and H. Nishide, J. Chem. Soc., Dalton Trans., 2713 (1990).
20. M. Momenteau, J. Mispelter, B. Loock, and E. Bisagni, J. Chem. Soc., Perkin Trans., 1, 189 (1983).