Preparation of Bis-Functionalized 1,4-Diaminobutane Derivatives

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Abstract:

A three-component solvent-free method for the synthesis of a series of bis-α-aminophosphonate-modified butanes has been developed. The experimental results showed that the solvent-free reaction conditions without catalyst were optimal for the preparation of this type compounds. The synthesized title compounds were characterized by 1H, 13C, and 31P NMR and mass spectroscopy.

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63-66

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October 2014

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© 2014 Trans Tech Publications Ltd. All Rights Reserved

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[1] Karine Vercruysse-Moreira, Christophe Dejugnat, Guita Etemad-Moghadam, Tetrahedron. Vol. 58 (2002), p.5651.

Google Scholar

[2] Y. Okahata, T. Kunitake, J. Am. Chem. Soc. Vol. 101 (1979), p.5231.

Google Scholar

[3] T. Shimizu, M. Kogiso, M. Masuda, J. Am. Chem. Soc. Vol. 119 (1997), p.6209.

Google Scholar

[4] K.S. Suslick, M.W. Grinstaff, J. Am. Chem. Soc. Vol. 112 (1990), p.7807.

Google Scholar

[5] M. Lawrence, J. Chem. Soc. Rev. (1994), p.417.

Google Scholar

[6] Karine Vercruysse-Moreira, Christophe Dejugnat, Guita Etemad-Moghadam Tereahedron Vol. 58 (2002), p.5651.

Google Scholar

[7] H.J. Cristau, P. Mouchet, J.F. Dozol, H. Rouquette, Heteroat. Chem. Vol. 6 (1995), p.533.

Google Scholar

[8] A.W. Herlinger, R. Chiarizia, J.R. Ferraro, P.G. Rickert, E.P. Horwitz, Solvent Extr. Ion Exch. Vol. 15 (1997), p.401.

Google Scholar

[9] A. Hille, R. Gust, Arch. Pharm. Chem. Life Sci. Vol. 342 (2009), p.625.

Google Scholar

[10] J.S. Yadav, B.V.S. Reddy, P. Sreedhar, Green Chem. Vol. 4 (2002) p.436.

Google Scholar

[11] B. Kaboudin, K. Moradi, Tetrahedron Lett. Vol. 46 (2005), p.2989.

Google Scholar

[12] Z.P. Zhan, R.F. Yang, J.P. Li, Chem. Lett. Vol. 34 (2005), p.1042.

Google Scholar

[13] H. Firouzabadi, N. Iranpoor, S. Sobhani, Synthesis (2004), p.2696.

Google Scholar

[14] C. Qoam, T. Huang, J. Org. Chem. Vol. 63 (1998), p.4125.

Google Scholar

[15] K. Manabe, S. Kobayashi, Chem. Commun (2000), p.669.

Google Scholar