Microwave enhanced synthesis of 5-arylidene rhodanine under solvent free conditions using bismuth trichloride as a promoter

Rasayan Journal of Chemistry

Volumn 1, Issue 4, 2008, Pages 738-742

  Bhatti, Ravinder S ^a   Singh, Manjit ^a   Sandhu, Jagir S ^a  

^a PUNJABI UNIVERSITY   (India)

Author keywords

2,4 thiazolidinedione; Aldehydes; Microwave; Rhodanines; Solvent free

Indexed keywords

EID: 84902675976     PISSN: 09741496     EISSN: 09760083     Source Type: Journal    
DOI: None     Document Type: Article

References (27)

1. R A Sheldon, Chem. Ind (London) 12(1997).
2. J H Clark, Chemistry of waste minimization, (Chapman and Hall, London), 1995
3. J H Clark, & D J Macquarrie, Chem Soc Rev 303(1996)
4. F Toda, K Tanaka & A Sekikawa. J Chem. Soc. Chem Commum, 279(1987).
5. For reviews on solvent free organic synthesis see: (1) F Todda, Acc Chem Res 480(1995).
6. K Tanaka & F Todda, Chem Rev, 1024(2000).
7. D C Dittmer, Chem Ind 779(1997).
8. N Hall, Science 266, 32(1994)
9. T. Sohda, K. Mizumo, E. Imamiya, H. Tawada, K. Meguro, Yamamoto Y. Kawamastu, Chem. Pharm. Bull 30, 3601(1982)
10. M. J. Reginato and M. A. Lazar, TEM, 10, 9(1999); B. B. Zhang and D. E. Muller, Current Opinion in Chemical Biology, 4, 461(2000)
11. S. K. Shukla, S. P. Singh, L. P. Awasthi and D. D. Mukherjee, Indian J. Pharm. Sci., 44, 153(1982);Chem. Abtstr. 99, 22365u (1983)
12. G. Captan, N. Ulusoy, N. Ergenc, A. C. Ekinic and A. Vidin, Il Farmaco, 51, 729(1996);Chem. Abstr., 126, 157436q (1996)
13. W. T. Sing, C. L. Lee, S. L. Yeo, S. P. Lim and M. M. Sim, Biorg. Med. Chem. Lett. 11, 91(2001)
14. M. M. Sim, S. B. Ng, A. D. Buss, S. C. Crasta, K. L. Goh and S. K. Lee, Biorg. Med. Chem. Lett, 12, 697(2002);
15. G Bruna, L. Costantino, C. Curinga, R. Maccari, F. Monforte, F. Nicolo, R. Ottana and M. G. Vigorita, Bioorg. Med. Chem. Lett., 12, 1077(2002)
16. D. Libermann, J. Himbert and L. Hengl, Bull. Soc. Chim. France, 4, 1120(1948);
17. D. A. Heerding, L. T. Christmann, T. J. Clark, D. J. Holmes, S. F. Rittenhouse, D. T. Takata and J. W. Venslavsky, Bioorg. Med. Chem. Lett, 13, 3771(2003);
18. K. Popov-Pergal, Zh. Chekovich and M. Pergal, Zhur. Obshch. Khim 61, 2112(1994)
19. A. Corma, V. Forne, R. M. Martin-Aranda, H. Garcia and Primo, J. Appl. Catal. 59, 237(1990); J. Muzart, Synth. Commun 15, 285(1985)
20. J.-F. Zhou, F.-X. Zhu, Y.-Z. Song and Y.-L. Zhu, ARKIVOC (xiv), 175(2006)
21. D. Prajapati and J. S. Sandhu, Chemistry Letters 1945(1992); B. Baruah, D. Prajapati, A Baruah and J. S. Sandhu, Tetrahedron Letters 1449-1450(1997).
22. M. Wada, H. Ohki, K. Y. Akiba, Bull. Chem. Soc. Jpn. 63, 1738(1990);
23. H. Suzuki, T. Ikegami, Y. Matano, Synthesis 249(1997)
24. S. Vidal, Synlett Spotlight 31, Synlett 1194(2001).
25. M. Sortino, P. Delgado, S. Juarez, J. Quiroga, R. Abonia, B. Insuasty, M. Nogueras, L. Rodero, F. M. Garibotto, R. D. Enriz and S. A. Zacchino, Bioorg. Med. Chem. 15, 484(2007).
26. R. G. Giles, N. J. Lewis, J. K. Quick, M. J. Sasse, M. W. J. Urquhart and L. Youssef, Tetrahedron, 56, 4531(2000);
27. G. W. Sawdey, M. K. Ruoff and P. W. Vittum, J. Am. Chem. Soc., 72, 4947(1950).