Green and expeditious synthesis of 1,8-dioxodecahydroacridine derivatives catalysed by protic pyridinium ionic liquid

Journal of Chemical Sciences

Volumn 125, Issue 6, 2013, Pages 1517-1522

  Alinezhad, Heshmatollah ^a   Tajbakhsh, Mahmood ^a   Norouzi, Mohammad ^a,b   Baghery, Saeed ^c,d   Rakhtshah, Jamshid ^c  

^a UNIVERSITY OF MAZANDARAN   (Iran)

^b PAYAME NOOR UNIVERSITY   (Iran)

^c BU ALI SINA UNIVERSITY   (Iran)

^d ISLAMIC AZAD UNIVERSITY   (Iran)

Author keywords

1,8 dioxodecahydroacridine; water solvent; 2 Methylpyridinium trifluoromethanesulphonate; Hantzsch three component condensation; Protic ionic liquid

Indexed keywords

CONDENSATION; CONDENSATION REACTIONS;

2-METHYLPYRIDINIUM TRIFLUOROMETHANESULPHONATE; ANILINE DERIVATIVES; EFFICIENT CATALYSTS; EXPEDITIOUS SYNTHESIS; PROTIC IONIC LIQUIDS; PYRIDINIUM IONIC LIQUID; THREE COMPONENT; WATER SOLVENTS;

IONIC LIQUIDS;

EID: 84896762064     PISSN: 09743626     EISSN: 09737103     Source Type: Journal    
DOI: 10.1007/s12039-013-0517-4     Document Type: Article

References (37)

1. Zhao D,Wu M, Kou Y and Min E 2002 Catal. Today 74 157
2. Lu W, Fadaev A G, Qu B, Smela E, Mattes B R, Ding J, Spinks G M, Mazurkiewicz J, Zhou D, Wallace G G, Mac Farlane D R, Forsyth S A and Forsyth M 2002 Science 297 983
3. Welton T 2004 Coord. Chem. Rev. 248 2459
4. Bhatt A I, Mechler A, Martin L L and Bond A M 2007 J. Mater. Chem. 17 2241
5. Liu J F, Jonsson J A and Jiang J B 2005 Trends. Anal. Chem. 24 20
6. Wang R, Okajima T, Kitamura F and Ohsaka T 2004 Electroanalysis 16 66
7. Liu J F, Jo L, Wang M, Li Z, Liu H and Li J 2005 Green Chem. 7 655
8. Bicak N 2005 J. Mol. Liq. 116 15
9. Kidwai M and Bahatnagar D 2010 Chem. Papers 64 825
10. Kimura M, Kato A and Okabayashi I 1992 J. Heterocycl. Chem. 29 73
11. Josephrajan T, Ramakrishanan V T and Muthumary J 2005 ARKIVOC xi 124
12. Heald R A and StevensMF G 2003 Org. Biomol. Chem. 1 3377
13. Michon V and Tombret F 1995 Eur. J. Med. Chem. 30 147
14. Moskural R, Hoke L and Gaudiana R A 2006 J. Macromol. Sci. Part. A. Pure. Appl. Chem. 43 1907
15. Kumar A, Sharma S and Srivastave V K 2003 Indian J. Chem. 42B 1779
16. Sondhi S M and Bhattacharjee G 2004 Cent. Eur. J. Chem. 2 1
17. Gutsulyak Kh V, Manzhara V S, Melnik M V and Kalin T I 2005 J. Appl. Spect. 72 488
18. Papagni A, Campiglio P and CampioneM2008 J. Fluor. Chem. 129 294
19. Subba B V, Antony A and Yadav J S 2010 Tetrahedron Lett. 51 3071
20. Bakibaev A A, Fillimonov V D and Nevgodova E S 1991 Zh. Org. Khim. 27 1519
21. Kaya M, Yildirir Y and Celik G Y 2011 Med. Chem. Res. 20 293
22. Kidwai M and Bhatanagar D 2010 Tetrahedron Lett. 51 2700
23. Suárez M, Loupy A, Salfrán E, Morán L and Rolando E 1999 Heterocycles 51 21
24. Martin N, Quinteiro M, Seoane C, Soto J L, Mora A, Suarez M, Morales A, Ochoa E and Bosque J D 1995 J. Heterocycl. Chem. 32 235
25. Das B, Thirupathi P, Mahender I, Reddy V S and Rao Y K 2006 J. Mol. Catal. A. Chem. 247 233
26. Jin T S, Zhang J S, Guo T T,Wang A Q and Li T S 2004 Synthesis 12 2001
27. Wang X S, Shi D Q, Zhang Y F, Wang S H and Tu S J 2004 Chin. J. Org. Chem. 24 430
28. Li Y L, Zhang M M, Wang X S, Shi D Q, Tu S J, Wei X Y and Zong Z M 2005 J. Chem. Res. S. 600
29. Wang G W, Xia J J, Miao C B and Wu X L 2006 Bull. Chem. Soc. Jpn. 79 454
30. Wang X S, Zhang M M, Jiang H, Shi D Q, Tu S J, Wei X Y and Zong Z M 2006 Synthesis 24 4187
31. Shen W, Wang L M, Tian H, Tang J and Yu J J 2009 J. Fluor. Chem. 130 522
32. Dabiri M, Baghbanzadeh M and Arzroomchilar E 2008 Catal. Commun. 9 939
33. Li C J and Chan T H 1997 Organic reaction in aqueous media (New York: Wiley)
34. Duan Z, Gu Y, Zhang J, Zhu L and Deng Y 2006 J. Mol. Catal. A. Chem. 250 163
35. Vahdat S M, Mardani H R, Golchoubian H, Khavarpour M, Baghery S and Roshankouhi Z 2013 Comb. Chem. High. T. Scr. 16 2
36. Venkatesan K, Pujari S S and Srinivasan K V 2009 Synth. Commun. 39 228
37. Chandrasekhar S, Rao Y S, Sreelakshmi L, Mahipal B and Reddy C R 2008 Synthesis 11 1737