An efficient and green method for the synthesis of oxindole derivatives in water

Chemistry Letters

Volumn 37, Issue 3, 2008, Pages 268-269

  Srihari, G ^a   Marthanda Murthy, M ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 42049114740     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2008.268     Document Type: Article

References (20)

1. W. G. Rajeswaran, R. B. Labroo, L. A. Cohen, M. M. King, J. Org. Chem. 1999, 64, 1369.
2. a) F. D. Popp, J. Heterocycl. Chem. 1984, 1641.
3. b) H. Pajouhesh, R. Parsons, F. D. Popp. J. Pharmacol. Sci. 1983, 318.
4. c) K. C. Joshi, V. N. Pathak, S. K. Jain, Pharmazie 1980, 677.
5. R. J. Sundberg, The Chemistry of Indoles, Academic, New York, 1996.
6. Y. Kamano, H. Zhang, Y. Ichihara, H. Kizu, K. Komiyama, H. Itokawa, G. R. Pettit, Tetrahedron Lett. 1995, 36, 2783.
7. G. K. Jnaneshwar, V. H. Deshpande, J. Chem. Res. (S) 1999, 632.
8. a) D. A. Klumpp, K. Y. Yeung, G. K. S. Prakash, G. A. Olah, J. Org. Chem. 1998, 63, 4481.
9. b) D. P. Franklin. Ger. Pat. 2258505, 1973.
10. c) B. S. Jursic, E. D. Stevens, Tetrahedron Lett. 2002, 43, 5681.
11. J. Azizian, A. A. Mohammadi, N. Karimi, M. R. Mohammadizadeh, A. B. Karimi, Catal. Commun. 2006, 7, 752.
12. J. S. Yadav, B. V. S. Reddy, K. U. Gayatri, S. Meraj, A. R. Prasad, Synthesis 2006, 4121.
13. S.-Y. Wang, S.-J. Ji, Tetrahedron 2006, 62, 1527.
14. a) Y. Seno, S. Shiraishi, Y. Suzuki, T. Asahara, Bull. Chem. Soc. Jpn. 1978, 51, 1413.
15. b) S. Sarel, J. Klug, E. Breaer, F. D'Angeli, Tetrahedron Lett. 1964, 5, 1553.
16. c) M. Chakrabarthy, R. Mukherjee, A. Mukherji, S. Arima, Y. Harigaya, Heterocycles 2006, 68, 1659.
17. d) M. Chakrabarty, S. Sarkar, Y. Harigaya, J. Chem. Res. 2005, 540.
18. a) Organic Synthesis in Water, ed. by P. A. Grieco, Black Academic and Professional, London, 1998.
19. b) C. J. Li, T. H. Chan, Organic Reactions in Aqueous Media, John Wiley & Sons, New York, 1997.
20. General procedure for synthesis of oxindole derivatives: A mixture of isatins (1 mmol) and indoles/pyrrole (2 mmol) taken in deionized water (2 mL) was refluxed for the appropriate time as mentioned in the Tables 1 and 2. The reaction was monitored by TLC. The product was filtered and the crude product was crystallized from ethanol.