Pure Appl. Chem., 2010, Vol. 82, No. 3, pp. 577-582
http://dx.doi.org/10.1351/PAC-CON-09-11-06
Published online 2010-02-14
Asymmetric synthesis of aminophosphonic acids mediated by chiral sulfinyl auxiliary: Recent advances
References
- 1. For an excellent monograph, see: V. P. Kukhar, H. R. Hudson (Eds.). Aminophosphonic and Aminophosphinic Acids: Acids: Chemistry and Biological Activity, John Wiley, New York (2000).
 - 2. P. , B. Lejczak. Phosphorus, Sulfur, Silicon Relat. Elem. 63, 193 (1991). (http://dx.doi.org/10.1080/10426509108029443)
 - 3a. M. , P. Łyżwa, J. Drabowicz, M. W. Wieczorek, J. Błaszczyk. Chem. Commun. 568 (1996).
 - 3b. M. , P. Łyżwa, J. Drabowicz. Tetrahedron: Asymmetry 8, 3991 (1997). (http://dx.doi.org/10.1016/S0957-4166(97)00606-X)
 - 3c. M. , P. Łyżwa, J. Drabowicz. Tetrahedron: Asymmetry 13, 2571 (2002). (http://dx.doi.org/10.1016/S0957-4166(02)00684-5)
 - 3d. for a summary of our work, see: M. . J. Organomet. Chem. 690, 2488 (2005). (http://dx.doi.org/10.1016/j.jorganchem.2004.10.045)
 - 4a. For recent reviews on the synthesis of α- and β-aminophosphonic acids, see: M. , H. Rojas-Cabrera, C. Cativiela. Tetrahedron 65, 17 (2009). (http://dx.doi.org/10.1016/j.tet.2008.09.083)
 - 4b. F. , C. Alonso, J. M. de los Santos. Chem. Rev. 105, 899 (2005). (http://dx.doi.org/10.1021/cr040672y)
 - 5a. For recent syntheses of enantiomeric AP4, see: G. , V. Maranon, C. G. Avila-Ortiz, C. Anaya de Parrodi, L. Quintero, E. Juaristi. Tetrahedron 62, 8404 (2006). (http://dx.doi.org/10.1016/j.tet.2006.06.018)
 - 5c. M. C. , A. Diaz, J. J. Guillin, O. Blanco, M. Ruiz, V. Ojea. J. Org. Chem. 71, 6958 (2006). (http://dx.doi.org/10.1021/jo061072x)
 - 5b. Ch. , C. Goudet, N. Queslati, J.-P. Pin, F. C. Acher. J. Med. Chem. 50, 4656 (2007). (http://dx.doi.org/10.1021/jm070400y)
 - 6. Z. H. , A. Koty?ski, G. Andrijewski. J. Organomet. Chem. 479, 199 (1994). (http://dx.doi.org/10.1016/0022-328X(94)84109-8)
 - 7. F. A. , Y. Zhang, Y. Andemichael, T. Fang, D. L. Fanelli, H. Zhang. J. Org. Chem. 64, 1403 (1999). (http://dx.doi.org/10.1021/jo9820622)
 - 8. For absolute configuration of (–)-20, see: A. , R. Voeffray. Helv. Chim. Acta 65, 1953 (1982). (http://dx.doi.org/10.1002/hlca.19820650702)
 
