Microwave assisted oxidation coupling of thiols to symmetrical disulfides with tripropylammonium fluorochromate (VI) (TPAFC)
Subject Areas : Journal of the Iranian Chemical ResearchMohammad Kazem Mohammadi 1 , Neda Hasanzadeh 2 , Shahriare Ghammamy 3
1 - Islamic Azad University, Ahvaz Branch , Faculty of Science, Ahvaz , Iran
2 - Islamic Azad University, Ahvaz Branch , Faculty of Science, Ahvaz , Iran
3 - Department of Chemistry, Faculty of Science, Imam Khomeini International University, Qazvin, Iran
Keywords:
Abstract :
[1] L.F. Fieser, M. Fieser, Reagents for Organic Synthesis, Wiley, New York, 1967.
[2] D.C .Jocelyn, Biochemistry of the Thiol Group, Academic Press, New York, 1992.
[3] G. Capozzi, G. Modena, S. Patai, The Chemistry of the Thiol Group, Wiley, New York, 1974.
[4] J. Lam, H. Bildose, L.P. Christensen, T. Thomsen, Acta Chem. Scand. Ser B 43 (1989) 799-
803.
[5] V. Srivastav, R. Gupta, R.R. Guptam, Ind. J. Chem. 39B (2000) 223-227.
N. Hasanzadeh & et al. / J. Iran. Chem. Res. 3 (2010) 155-160
160
[6] P. Metzner, Synthesis (1978) 669-674.
[7] D.L. Holbrook, Handbook of Petroleum Refining Processes, R.A. Meyers (Edi,) McGraw
Hill, 1996.
[8] A. Leitao, C. Costa, A. Rodrigues, Chem. Eng. Sci. 42 (1987) 2291-2298.
[9] E.P. Papadopoulos, A. Jarrar, C. H.Issidoides, J. Org. Chem. 31 (1966) 615-620.
[10] C. Lopez, F. Conzales, P. Cossio, C. Palomo, Synth. Commun. 15 (1985) 1197-1206.
[11] J.M. Aizpurua, M. Juaristu, B. Lecea, C. Palomo, Tetrahedron 41 (1985) 2903-2908.
[12] F. Yoneda, K. Suzuki, Y. Nitta, J. Org. Chem. 32 (1967) 727-735.
[13] K. Nakagawa, S. Shiba, M. Horikawa, K. Sato, H. Nakamura, N. Harada, F. Harada, Synth.
Commun. 10 (1980) 305-311.
[14] H. Firouzabadi, N. Iranpoor, F. Kiaeezadeh, J. Toofan, Tetrahedron 42 (1986) 719-726.
[15] S.V. Ley, A. Meerholz, D.H.R. Barton, Tetrahedron 37 (1982) 231-239.
[16] H.A. Muathen, Ind. J. Chem. 30B (1991) 522-530.
[17] A. Mckillop, D. Koyuncu, A. Krief, W. Dumont, P. Renier, M. Trabelsc, Tetrahedron Lett.
31 (1990) 5007-5011.
[18] H. Tamamura, A. Otaka, J. Nakamura, K. Okubo, T. Koide, K. Ikeda, N. Fujii, Tetrahedron
Lett. 34 (1993) 4931-4936.
[19] N.A. Noureldin, M. Coldwell, J. Hendry, D.G. Lee, Synthesis (1998) 1587-1595.
[20] (a) R.A. Abramovitch, Org. Prep. Proc. Int. 23 (1991) 683-689, (b) G. Majetich, R.J. Elec, Energy 30
(1995) 27-38, (c) S. Caddick, Tetrahedron 51 (1995) 10403-10409, (d) C.R. Strauss, R.W. Trainor,
Aust. J. Chem. 48 (1995) 1665-1672.
[21] (a) D. Bogdal, M. Warzala, Tetrahedron 56 (2000) 8769-8775, (b) D. Bogdal, J. Chem. Res. (1998)
468-472, (c) D. Bogdal, J. Pielichowski, K. Jaskot, Org. Prep. Proc. 30 (1998) 427-434.
[22] N. Iranpoor, B. Zeynizadeh, Synthesis (1999) 49-56.