Synthesis of P1, P3-Distavudine-5′, 5′-Triphosphate

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A practical method for the preparation of P1,P3-distavudine triphosphate has been developed. Stavudine diphosphate was first synthesized from stavudine phosphoropiperidate. The coupling of stavudine diphosphate with excess stavudine phosphoropiperidate in the presence of 4,5-dicyanoimidazole afforded symmetrical distavudine triphosphate in good yield.

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August 2014

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© 2014 Trans Tech Publications Ltd. All Rights Reserved

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[1] R.K. Robins, Med. Res. Rev. Vol. 3 (1985) p.273.

Google Scholar

[2] R.J. Jones, N. Bischofberger, Antiviral Res. Vol. 27 (1995) p.1.

Google Scholar

[3] D. Clercq, Molecular Targets for Antiviral Agents. Vol. 297 (2000) p.1.

Google Scholar

[4] E. De Clercq, J. Neyts, Handb. Exp. Pharmacol. Vol. 189 (2009) p.53.

Google Scholar

[5] B. Öberg, Antiviral Res. Vol. 71 (2006) p.90.

Google Scholar

[6] M. Baba, R. Pauwels, P. Herdewijn, E. De Clercq, J. Desmyter, M. Vandeputte, Biochem. Biophys. Res. Commun. Vol. 142 (1987), p.128.

Google Scholar

[7] J. Balzarini, S. Aquaro, T. Knispel, C. Rampazzo, V. Bianchi, C. -F. Perno, E. De Clercq, C. Meier, Mol. Pharmacol. Vol. 58 (2000) p.928.

DOI: 10.1124/mol.58.5.928

Google Scholar

[8] E. De Clercq, J. Med. Chem. Vol. 38 (1995) p.2491.

Google Scholar

[9] D. Saboulard, L. Naesens, D. Cahard, A. Salgado, R. Pathirana, S. Velazquez, C. McGuigan, E. De Clercq, J. Balzarini, Mol. Pharmacol. Vol. 56 (1999) p.693.

Google Scholar

[10] S. Yang, C. Pannecouque, P. Herdewijn, Chemistry Biodiversity. Vol. 9 (2012), p.2186.

Google Scholar

[11] S.R. Shaver, J.L. Rideout,W. Pendergast, J.G. Douglass, E.G. Brown, J.L. Boyer, R.I. Patel, C.C. Redick, A.C. Jones, M. Picher, B.R. Yerxa, Purinergic Signalling Vol. 1 (2005), p.183.

DOI: 10.1007/s11302-005-0648-2

Google Scholar

[12] W. Pendergast, B.R. Yerxa, J.G. Douglass, S.R. Shaver, R.W. Dougherty, C.C. Redick, I.F. Sims, J.L. Rideout, Bioorg. Med. Chem. Lett. Vol. 11 (2001), p.157.

DOI: 10.1016/s0960-894x(00)00612-0

Google Scholar

[13] S. Mohamady, S.D. Taylor, J. Org. Chem. Vol. 76 (2011), p.6344.

Google Scholar

[14] S. Mohamady, A. Desoky, S.D. Taylor, Org. Lett. Vol. 14 (2012), p.402.

Google Scholar

[15] Q. Sun, S. Gong, J. Sun, C. Wang, S. Liu, G. Liu, C. Ma, Tetrahedron Lett. Vol. 55 (2014), p.2114.

Google Scholar