Hexafluoroisopropanol dispersed into the nanoporous SBA-15 (HFIP/SBA-15) as a rapid, metal-free, highly reusable and suitable combined catalyst for domino cyclization process in chemoselective preparation of alkyl rhodanines

Journal of Fluorine Chemistry

Volumn 153, Issue , 2013, Pages 1-6

  Rostamnia, Sadegh ^a   Doustkhah, Esmail ^a   Nuri, Ayat ^a  

^a UNIVERSITY OF MARAGHEH   (Iran)

Author keywords

Fluorinated alcohol; Hexafluoroisopropanol (HFIP); Multicomponent reaction; SBA 15 nanoreactor; Thioxo thiophenecarboxylate

Indexed keywords

EID: 84879811628     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jfluchem.2013.05.025     Document Type: Article

References (23)

1. (a) R. Juarez, S.F. Parker, P. Concepcion, A. Corma, H. Garcia, Chem. Sci. 1 (2010) 731-738
2. (b) S. Navalon, R. Martin, M. Alvaro, H. Garcia, Angew. Chem. Int. Ed. Engl. 49 (2010) 8403-8407
3. (c) D. Mendes, H. Garcia, V.B. Silva, A. Mendes, L.M. Madeira, Ind. Eng. Chem. Res. 48 (2009) 430-439.
4. (a) S. Rostamnia, A. Zabardasti, J. Fluorine Chem. 144 (2012) 69-72
5. (b) J. Povey, C. Smales, S. Hassard, M.J. Howard, J. Struct. Biol. 157 (2007) 329-338.
6. (a) L. Eberson, M.P. Hartshorn, O. Perssona, F. Radnera, Chem. Commun. (1996) 2105-2112
7. (b) J.-P. Bégué, D. Bonnet-Delpon, B. Crousse, Synlett (2004) 18-29
8. (c) K. Uneyama, Organofluorine Chemistry, Blackwell Publishing Ltd., Oxford, 2006.
9. (a) A. Alizadeh, S. Rostamnia, N. Zohreh, R. Hosseinpour, Tetrahedron Lett. 50 (2009) 1533-1535
10. (b) S. Rostamnia, Z. Karimi, M. Ghavidel, J. Sulfur Chem. 33 (2012) 313-318
11. (c) S. Rostamnia, Investigation of the novel multicomponent reactions based on binucleophilic systems and zwitterions, Tarbiat Modares University, Tehran, Iran, 2010 (Ph.D. Dissertation).
12. M.G. Orchard, J.C. Neuss, C.M.S. Galley, A. Carr, D.W. Porter, P. Smith, D.I.C. Scopes, D. Haydon, K. Vousden, C.R. Stubberfield, K. Young, M. Page, Bioorg. Med. Chem. Lett. 14 (2004) 3975-3978.
13. (a) J.H. Ahn, S.J. Kim, W.S. Park, S.Y. Cho, J.D. Ha, S.S. Kim, S.K. Kang, D.G. Jeong, S.K. Jung, S.-H. Lee, H.M. Kim, S.K. Park, K.H. Lee, C.W. Lee, S.E. Ryu, J.K. Choi, Bioorg. Med. Chem. Lett. 16 (2006) 2996-2999
14. (b) N.S. Cutshall, C.O. Day, M. Prezhdo, Bioorg. Med. Chem. Lett. 15 (2005) 3374-3379.
15. (a) S. Rostamnia, A. Alizadeh, L.G. Zhu, J. Comb. Chem. 143 (2009) 143-145
16. (b) S. Rostamnia, K. Lamei, Synthesis (2011) 3080-3082
17. (c) S. Rostamnia, Res. J. Chem. Environ. 15 (2011) 89-91
18. (d) A. Alizadeh, S. Rostamnia, A. Esmaili, Synthesis (2007) 709-712
19. (e) S. Rostamnia, K. Lamei, M. Mohammadqoli, M. Sheykhan, A. Heydari, Tetrahedron Lett. 53 (2012) 5257-5260
20. (f) S. Rostamnia, K. Lamei, Chin. Chem. Lett. 23 (2012) 930-932
21. (g) A. Alizadeh, Q. Oskueyan, S. Rostamnia, Synthesis (2007) 2637-2640
22. (h) A. Alizadeh, N. Zohreh, S. Rostamnia, Tetrahedron 63 (2007) 8083-8087.
23. For the synthesis of high surface area SBA-15 see: D. Zhao, J. Feng, Q. Huo, N. Melosh, G.H. Fredrickson, B.F. Chmelka, G.D. Stucky, Science, 279 (1998) 548-552.