Ionic-liquids-assisted reaction of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes with β-nitrostyrenes

Mendeleev Communications

Volumn 19, Issue 5, 2009, Pages 276-278

  Syroeshkina, Yuliya S ^a   Kachala, Vadim V ^a   Ovchinnikov, Igor V ^a   Kuznetsov, Vladimir V ^a   Nelyubina, Yulia V ^b   Lyssenko, Konstantin A ^b   Makhova, Nina N ^a  

^a N D ZELINSKY INSTITUTE OF ORGANIC CHEMISTRY   (Russian Federation)

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

Author keywords

[No Author keywords available]

Indexed keywords

EID: 70349324385     PISSN: 09599436     EISSN: 1364551X     Source Type: Journal    
DOI: 10.1016/j.mencom.2009.09.016     Document Type: Article

References (17)

1. Syroeshkina Yu.S., Kuznetsov V.V., Lyssenko K.A., and Makhova N.N. Mendeleev Commun. 18 (2008) 42
2. Syroeshkina Yu.S., Kuznetsov V.V., Epishina M.A., Struchkova M.I., and Makhova N.N. Mendeleev Commun. 18 (2008) 207
3. Syroeshkina Yu.S., Kuznetsov V.V., Lyssenko K.A., and Makhova N.N. Izv. Akad. Nauk, Ser. Khim. (2009) 362 (in Russian)
4. O. W. Griffith and S. S. Gross, in Methods in Nitric Oxide Research, eds. M. Feelish and J. S. Stamler, John Wiley and Sons, Chichester, 1996, pp. 187-208.
5. Schottel B.L., Chifotides H.T., and Dunbar K.R. Chem. Soc. Rev. 37 (2008) 68
6. Golovanov D.G., Perekalin D.S., Yakovenko A.A., Antipin M.Y., and Lyssenko K.A. Mendeleev Commun. (2005) 237
7. Espinosa E., Alkorta I., Rozas I., Elguero J., and Molins E. Chem. Phys. Lett. 336 (2001) 457
8. Alarco P.-J., Abu-Lebdeh Ya., and Armand M. Solid State Ionics 175 (2004) 717
9. Houlihan W.J., and Theuer W.J. J. Org. Chem. 33 (1968) 3941
10. B. Kurosu, Japanese Patent 51133265 (A). (Chem. Abstr., 1977, 85, 63065a).
11. B. L. Walworth, US Patent 4091106 (A). (Chem. Abstr., 1978, 86, 16667j).
12. Pezdirc L., Jovanovski V., Bevk D., Jakše R., Pirc S., Meden A., Stanovnik B., and Svete J. Tetrahedron 61 (2005) 3977
13. Svetlic J., and Sallai L. J. Heterocycl. Chem. 39 (2002) 363
14. Kuznetsov V.V., Kutepov S.A., Makhova N.N., Lyssenko K.A., and Dmitriev D.E. Izv. Akad. Nauk, Ser. Khim. (1999) 623 (Russ. Chem. Bull., 1999, 48, 517)
15. G. M. Sheldrick, SHELXTL v. 5.10, Structure Determination Software Suite, Bruker AXS, Madison, Wisconsin, USA.
16. M. J. Frisch, G.W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, V. G. Zakrzewski, J. A. Montgomery, R. E. Stratmann, J. C. Burant, S. Dapprich, J. M. Millam, A. D. Daniels, K. N. Kudin, M. C. Strain, O. Farkas, J. Tomasi, V. Barone, M. Cossi, R. Cammi, B. Mennucci, C. Pomelli, C. Adamo, S. Clifford, J. Ochterski, G. A. Petersson, P. Y. Ayala, Q. Cui, K. Morokuma, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. Cioslowski, J. V. Ortiz, A. G. Baboul, B. B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R. Gomperts, R. L. Martin, D. J. Fox, T. A. Keith, M. A. Al-Laham, C. Y. Peng, A. Nanayakkara, M. Challacombe, P. M.W. Gill, B. Johnson, W. Chen, M. W. Wong, J. L. Andres, C. Gonzalez, M. Head-Gordon, E. S. Replogle and J. A. Pople, Gaussian 98, Revision A.9, Gaussian, Inc., Pittsburgh PA, 1998.
17. T. A. Keith, AIMAll (Version 08.01.25), 2008, http://aim.tkgristmill.com.