R. De Paula et al. / Journal of Molecular Catalysis A: Chemical 345 (2011) 1–11
11
[15] B. Meunier, Biomimetic Oxidations Catalyzed by Transition Metal Complexes,
Imperial College Press, London, 1999.
[53] S.L.H. Rebelo, M.M. Pereira, M.M.Q. Simões, M.G.P.M.S. Neves, J.A.S. Cavaleiro,
J. Catal. 234 (2005) 76–87.
[16] J.E. Backvall, Modern Oxidation Methods, Wiley-VCH, Weinheim, 2004.
[17] W.R. Sanderson, Pure Appl. Chem. 72 (2000) 1289–1304.
[18] M. Ghiasi, M. Tafazzoli, N. Safari, J. Mol. Struct. (Theochem.) 820 (2007) 18–25.
[19] T. Kamachi, T. Kouno, W. Nam, K. Yoshizawa, J. Inorg. Biochem. 100 (2006)
751–754.
[20] S.P. de Visser, J. Biol. Inorg. Chem. 11 (2006) 168–178.
[21] S. Jin, T.M. Makris, T.A. Bryson, S.G. Sligar, J.H. Dawson, J. Am. Chem. Soc. 125
(2003) 3406–3407.
[22] F. Montanari, S. Banfi, S. Quici, Pure Appl. Chem. 61 (1989) 1631–1636.
[23] F. Montanari, Pure Appl. Chem. 66 (1994) 1519–1526.
[24] A.M.A.R. Gonsalves, M.M. Pereira, J. Mol. Catal. A: Chem. 113 (1996) 209–221.
[25] R. Noyori, M. Aoki, K. Sato, Chem. Commun. (2003) 1977–1986.
[26] D. Rutkowska-Zbik, M. Witko, J. Mol. Catal. A: Chem. 258 (2006) 376–380.
[27] B. Meunier, A. Robert, G. Pratviel, J. Bernadou, in: K.M. Kadish, K.M. Smith, R.
Guilard (Eds.), The Porphyrin Handbook, Academic Press, 2000, p. 119.
[28] S. Banfi, M. Cavazzini, G. Pozzi, S.V. Barkanova, O.L. Kaliya, J. Chem. Soc. Perkin
Trans. 2 (2000) 871–877.
[54] J.T. Groves, W.J. Kruper, R.C. Haushalter, J. Am. Chem. Soc. 102 (1980)
6375–6377.
[55] J.T. Groves, M.K. Stern, J. Am. Chem. Soc. 109 (1987) 3812–3814.
[56] J.T. Groves, M.K. Stern, J. Am. Chem. Soc. 110 (1988) 8628–8638.
[57] Y.G. Abashkin, S.K. Burt, Inorg. Chem. 44 (2005) 1425–1432.
[58] K.J. Laidler, Pure Appl. Chem. 68 (1996) 149–192.
[59] A.A. Shteinman, Russ. Chem. Bull. 50 (2001) 1795–1810.
[60] S.-E. Park, W.J. Song, Y.O. Ryu, M.H. Lim, R. Song, K.M. Kim, W. Nam, J. Inorg.
Biochem. 99 (2005) 424–431.
[61] A. Agarwala, D. Bandyopadhyay, Catal. Lett. 124 (2008) 256–261.
[62] R.D. Arasasingham, G.X. He, T.C. Bruice, J. Am. Chem. Soc. 115 (1993)
7985–7991.
[63] S.P. de Visser, D. Kumar, S. Shaik, J. Inorg. Biochem. 98 (2004) 1183–1193.
[64] J.T. Groves, R.S. Myers, J. Am. Chem. Soc. 105 (1983) 5791–5796.
[65] Y. Liu, H.J. Zhang, Y.Q. Cai, H.H. Wu, X.L. Liu, Y. Lu, Chem. Lett. 36 (2007) 848–849.
[66] G.C. Bond, M.A. Keane, H. Kral, J.A. Lercher, Catal. Rev. 42 (2000) 323–383.
[67] B.K. Muralidhara, S.S. Negi, J.R. Halpert, J. Am. Chem. Soc. 129 (2007) 2015–2024.
[68] B.K. Muralidhara, L. Sun, S. Negi, J.R. Halpert, J. Mol. Biol. 377 (2008) 232–245.
[69] C.J. Bradaric, W.J. Leigh, J. Am. Chem. Soc. 118 (1996) 8971–8972.
[70] M.C. Curet-Arana, G.A. Emberger, L.J. Broadbelt, R.Q. Snurr, J. Mol. Catal. A:
Chem. 285 (2008) 120–127.
[29] L. Zeng, H.J.H. Wang, A. Lei, J.I. Brauman, J.P. Collman, Eur. J. Org. Chem. 2006
(2006) 2707–2714.
[30] A.C. Serra, E.C. Marc¸ alo, A.M.A.R. Gonsalves, J. Mol. Catal. A: Chem. 215 (2004)
17–21.
[31] H. Turk, M. Erdem, J. Porphyrins Phthalocyanines 8 (2004) 1196–1203.
[32] R. Belal, M. Momenteau, B. Meunier, J. Chem. Soc. Chem. Commun. (1989)
412–414.
[71] A.M. Khenkin, D. Kumar, S. Shaik, R. Neumann, J. Am. Chem. Soc. 128 (2006)
15451–15460.
[72] F. DeAngelis, N. Jin, R. Car, J.T. Groves, Inorg. Chem. 45 (2006)
4268–4276.
[33] S.P. deVisser, Inorg. Chem. 45 (2006) 9551–9557.
[34] N.A. Stephenson, A.T. Bell, J. Mol. Catal. A: Chem. 272 (2007) 108–117.
[35] A.A. Guedes, A. Santos, M.D. Assis, Kinet. Catal. 47 (2006) 555–563.
[36] M.D. Assis, A.O.J.B. Melo, P.B. Pereira, O.A. Serra, Y. Iamamoto, M. Moraes, J.
Inorg. Biochem. 51 (1993) 263–292.
[37] Y. Iamamoto, M.D. Assis, K.J. Ciuffi, C.M.C. Prado, B.Z. Prellwitz, M. Moraes, O.R.
Nascimento, H.C. Sacco, J. Mol. Catal. A: Chem. 116 (1997) 365–374.
[38] S.S. Kurek, P. Michorczyk, A.M. Balisz, J. Mol. Catal. A: Chem. 194 (2003)
237–248.
[73] D. Lahaye, J.T. Groves, J. Inorg. Biochem. 101 (2007) 1786–1797.
[74] N. Jin, M. Ibrahim, T.G. Spiro, J.T. Groves, J. Am. Chem. Soc. 129 (2007)
12416–12417.
[75] J.T. Groves, W.J. Kruper, J. Am. Chem. Soc. 101 (1979) 7613–7615.
[76] N. Jin, J.T. Groves, J. Am. Chem. Soc. 121 (1999) 2923–2924.
[77] W.J. Song, M.S. Seo, S. DeBeer George, T. Ohta, R. Song, M.J. Kang, T.
Tosha, T. Kitagawa, E.I. Solomon, W. Nam, J. Am. Chem. Soc. 129 (2007)
1268–1277.
[39] D. Kumar, S.P. de Visser, S. Shaik, Chem. Eur. J. 11 (2005) 2825–2835.
[40] Y. Liu, H.J. Zhang, Y. Lu, Y.Q. Cai, X.L. Liu, Green Chem. 9 (2007) 1114–1119.
[41] M. Fontecave, D. Mansuy, J. Chem. Soc. Chem. Commun. (1984) 879–881.
[42] A.M.A.R. Gonsalves, A.C. Serra, J. Chem. Soc. Perkin Trans. 2 (2002) 715–719.
[43] J.P. Collman, T. Kodadek, J.I. Brauman, J. Am. Chem. Soc. 108 (1986) 2588–2594.
[44] Y. Miyazaki, A. Satake, Y. Kobuke, J. Mol. Catal. A: Chem. 283 (2008) 129–139.
[45] R. De Paula, M.M.Q. Simões, M.G.P.M.S. Neves, J.A.S. Cavaleiro, Catal. Commun.
10 (2008) 57–60.
[46] R. De Paula, M.A.F. Faustino, D.C.G.A. Pinto, M.G.P.M.S. Neves, J.A.S. Cavaleiro, J.
Heterocycl. Chem. 45 (2008) 453–459.
[47] A.M.A.R. Gonsalves, J.M.T.B. Varejao, M.M. Pereira, J. Heterocycl. Chem. 28
(1991) 635–640.
[48] J.P.C. Tomé, M.G.P.M.S. Neves, A.C. Tomé, J.A.S. Cavaleiro, M. Soncin, M. Maga-
raggia, S. Ferro, G. Jori, J. Med. Chem. 47 (2004) 6649–6652.
[49] A.M.A.R. Gonsalves, M.M. Pereira, A.C. Serra, R.A.W. Johnstone, M.L.P.G. Nunes,
J. Chem. Soc. Perkin Trans. 1 (1994) 2053–2057.
[50] D.H. Tjahjono, T. Akutsu, N. Yoshioka, H. Inoue, Biochim. Biophys. Acta (BBA):
Gen. Subjects 1472 (1999) 333–343.
[51] J.D. Crapo, B.J. Day, M.P. Trova, P.J.F. Gauuan, D.B. Kitchen, I. Fridovich, I. Batinic-
Haberle, in: U.S. Patent (Ed.), Substituted Porphyrins, National Jewish Medical
and Research Center, Aeolus Pharmaceuticals Inc., Duke University, USA, 2003,
pp. 1–39.
[52] S.L.H. Rebelo, Metaloporfirinas: síntese e oxidac¸ ão catalítica de compostos
orgânicos com peróxido de hidrogénio, Departamento de Química, Universi-
dade de Aveiro, Aveiro/Portugal, 2003.
[78] A. Takahashi, T. Kurahashi, H. Fujii, Inorg. Chem. 46 (2007) 6227–6229.
[79] C. Hansch, A. Leo, R.W. Taft, Chem. Rev. 91 (1991) 165–195.
[80] J. Shorter, Pure Appl. Chem. 69 (1997) 2497–2510.
[81] N.W.J. Kamp, J.R.L. Smith, J. Mol. Catal. A: Chem. 113 (1996) 131–145.
[82] S. Campestrini, A. Cagnina, J. Mol. Catal. A: Chem. 150 (1999) 77–86.
[83] I.D. Cunningham, Ann. Rep. Prog. Chem., Sect. B: Org. Chem. 93 (1997) 27–41.
[84] I.D. Cunningham, Ann. Rep. Prog. Chem., Sect. B: Org. Chem. 94 (1998) 273–288.
[85] J. Clayden, N. Greeves, S. Warren, P. Wothers, Organic Chemistry, Oxford Uni-
versity Press, New York, 2001.
[86] P.R. Ortiz de Montellano, Cytochrome P450: Structure, Mechanism and Bio-
chemistry, third ed., Kluwer Academic/Plenum Publisher, New York, 2005.
[87] W.J. Song, Y.O. Ryu, R. Song, W. Nam, J. Biol. Inorg. Chem. 10 (2005) 294–304.
[88] Z. Pan, M. Newcomb, Inorg. Chem. 46 (2007) 6767–6774.
[89] T.S. Lai, S.K.S. Lee, L.L. Yeung, H.Y. Liu, I.D. Williams, C.K. Chang, Chem. Commun.
(2003) 620–621.
[90] J.A.A.W. Elemans, E.J.A. Bijsterveld, A.E. Rowan, R.J.M. Nolte, Eur. J. Org. Chem
(2007) 751–757.
[91] D.V. Deubel, C. Loschen, G. Frenking, in: G. Frenking (Ed.), Theoretical Aspects
of Transition Metal Catalysis (Topics in Organometallic Chemistry), Springer-
Verlag, Berlin, 2005, pp. 109–144.
[92] K.A. Joergensen, B. Schioett, Chem. Rev. 90 (1990) 1483–1506.
[93] M.C. Curet-Arana, R.Q. Snurr, L.J. Broadbelt, in: S.T. Oyama (Ed.), Mechanism in
Homogeneous and Heterogeneous Epoxidation Catalysis, Elsevier, Amsterdam,
2008, pp. 471–486.