Advantages of organophosphorus synthesis in ionic liquids: "Green" approaches to useful phosphorus-substituted building blocks

Phosphorus, Sulfur and Silicon and the Related Elements

Volumn 183, Issue 2-3, 2008, Pages 383-388

  Odinets, I L ^a   Matveeva, E V ^a   Sharova, E V ^a   Artyushin, O I ^a   Kozlov, V A ^a   Vorob'eva, D V ^a   Osipov, S N ^a   Roschenthaler G V ^b  

^a A N NESMEYANOV INSTITUTE OF ORGANOELEMENT COMPOUNDS   (Russian Federation)

^b UNIVERSITY OF BREMEN   (Germany)

Author keywords

1,2,3 triazoles; Amidation; Azidoalkylphosphonates; Carbamoylmethyl phoshine oxides; Click chemistry; Ionic liquids; Nucleophilic displacement reactions; The Michaelis Arbuzov reaction

Indexed keywords

EID: 45849089855     PISSN: 10426507     EISSN: 15635325     Source Type: Journal    
DOI: 10.1080/10426500701735130     Document Type: Conference Paper

References (9)

1. R. D. Rogers and K. R. Seddon, Eds. In Ionic Liquids as Green Solvents: Progress and Prospects, ACS Symposium Ser. (Washington, DC, 2003).
2. G. Keglevich, Z. Baan, Z. Finta, I. Hermecz, T. Novak, and I. L. Odinets, Curr. Org. Chem., 11, 107 (2007).
3. G. V. Kryshtal, G. M. Zhdankina, and S. G. Zlotin, Mendeleev Commun. 176 (2002).
4. S.-Gi. Lee, J. H. Park, J. Kang, and J. K. Lee, Chem. Commun., 1698 (2001).
5. J. S. Yadav, B. V. S. Reddy, and P. Sreedhar, Green Chem., 4, 436 (2002).
6. T. Yoshino, S. Imori, and H. Togo, Tetrahedron Lett., 62, 1309 (2006).
7. L. Crowhurst, N. L. Lancaster, J. M. Pérez Arlandis, and T. Welton, J. Am. Chem. Soc. 126, 11,549 (2004).
8. E. V. Matveeva, I. L. Odinets, V. A. Kozlov, A. S Shaplov, and T. A. Mastryukova, Tetrahedron Lett., 47, 7645 (2006).
9. M. Volland, V. Seitz, M. Maase, M. Flores, R. Papp, K. Massonne, V. Stegmann, K. Halbritter, R. Noe, M. Bartsch, W. Siegel, M. Becker, and O. Huttenloch. PCT Int. Patent Appl., WO 2003062251 (2003); Chem. Abstr., 139, 149,757 (2003).