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Synthesis and Characterization of Novel Phosphorictriamide Derivatives with Morpholine Substituents: Crystal Structures of Substituents: Crystal Structures of (CF3)C(O)NHP(O)(NC4H8O)2 and (p-Br-C6H4)C(O)NHP(O)(NC4H8O)2

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Using phosphorus pentachloride as a substrate, carbacylamidophosphates of the general formula (R)C(O)NHP(O)(NC4H8O)2, where R = CH2Cl I; CHCl2 II; CCl3 III; CF3 IV; p-Me-C6H4V; p-Br-C6H4 VI; p-Cl-C6H4 VII, were prepared and characterized by 1H, 31P and 13C NMR, IR spectroscopy and elemental analysis. Different carboxylic amides attached to phosphorus nuclei affect on IR and NMR spectra. Three-bond coupling constants between phosphorus and carbon nucleus, 3J(P,Caliphatic) in the synthesized compounds, were greater than two-bond coupling constants, 2J(P,Caliphatic). The structures of IV and VI were determined by single-crystal X-ray diffraction techniques. The compounds IV and VI formed centrosymmetric dimers via intermolecular N-HźźźO=P hydrogen bonds.
Rocznik
Strony
393--402
Opis fizyczny
Bibliogr. 19 poz., rys.
Twórcy
autor
autor
  • Department of Chemistry, Faculty of Science, Tarbiat Modares University, P.O. Box 14115-175 Tehran, Iran
Bibliografia
  • 1. Gubina K.E., Ovchynnikov V.A., Amirkhanov V.M, Fischer H., Stumpf R. and Skopenko V.V., Z. Naturforsch., 55b, 576 (2000).
  • 2. Amirkhanov V.M., Ovchinnikov V.A., Turov A.V. and Skopenko V.V., Russ. J. Coord. Chem., 23, 126 (1997).
  • 3. Trush V.A., Domasevitch K.V., Amirkhanov V.M. and Sieler J., Z. Naturforsch., 54b, 451 (1999).
  • 4. Gholivand K., Shariatinia Z. and Pourayoubi M., Polyhedron, 25, 711 (2005).
  • 5. Barak D., Ordentlich A., Kaplan D., Barak R., Mizrahi D., Kronman C., Segall V., Velan B. and Shaerman A., Biochemistry, 39, 1156 (2000).
  • 6. Mallender W.D., Szegletes T. and Rosenberry T.L., Biochemistry, 39, 7753 (2000).
  • 7. Ouryupin A.B., Kadyko M.I., Petrovskii P.V. and Fedin E.I., Tetrahedron Asymm., 6, 1813 (1995).
  • 8. Zon G., Ludeman S.M. and Egan W., J. Am. Chem. Soc., 99, 5785 (1977).
  • 9. Baldwin A., Huang Z., Jounaidi Y. and Waxman D.J., Arch. Biochem. Biophys., 409, 197 (2003).
  • 10. Pang Y, Kollmeyer T.M., Hong F., Lee J., Hammond P.I., Haugabouk S.P. and Brimijoin S., Biochem. Biol, 10,491 (2003).
  • 11. Borch R.F., Joswig C. and Fries K.M., J. Med. Chem., 14, 2672 (1995).
  • 12. Mohe N.U., Padiva K.J. and Salunkhe M.M., Bioorg. Med. Chem., 11, 1419 (2003).
  • 13. Uchikawa O., Fukatsu K., Tokunoh R., Kawada M., Matsumoto K., Imai Y., Hinuma S., Kato K.,Nishikawa H., Hirai K., Miyamoto M. and Ohkawa S., J. Med. Chem., 45, 4222 (2002).
  • 14. Fem J. and Garciarafanell J., J. Med. Chem., 38, 3918 (1995).
  • 15. GholivandK., MojahedF., Alizadehgan A.M. and Bijanzadeh H.R., Z. Anorg. Allg. Chem., 1570 (2006).
  • 16. Gholivand K., Alizadehgan A.M., Firooz A.A., Khajeh K., Naderi-Manesh H. and Bijanzadeh H.R., J. Enz. Inhib. Med. Chem., 21, 105 (2006).
  • 17. Gholivand K. and Mojahed F., Z Anorg. Allg. Chem., 631, 1912 (2005).
  • 18. Gubina K.E. and Amirkhanov V.M., Z Naturforsch., 55b, 1015 (2000).
  • 19. Corbridge D.E.C., Phosphorus, an outline of its Chemistry, Biochemistry and Technology, Fifth Edition, Elsevier, The Netherlands 1995.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ6-0011-0026
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