A green procedure for the synthesis of 1,8-dioxodecahydroacridine derivatives under microwave irradiation in aqueous media without catalyst

Journal of Heterocyclic Chemistry

Volumn 47, Issue 2, 2010, Pages 363-367

  Tang, Zi Qiang ^a,b   Chen, Yan ^a   Liu, Chang Ning ^a   Cai, Ke Ying ^a   Tu, Shu Jiang ^c,d  

^a XUZHOU INSTITUTE OF TECHNOLOGY   (China)

^b Xuzhou Technician Institute   (China)

^c JIANGSU NORMAL UNIVERSITY   (China)

^d JIANGSU NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ACRIDINE DERIVATIVE; WATER;

ARTICLE; CHEMICAL STRUCTURE; ENVIRONMENT; LIQUID CULTURE; MICROWAVE IRRADIATION; SYNTHESIS;

EID: 77950312313     PISSN: 0022152X     EISSN: 19435193     Source Type: Journal    
DOI: 10.1002/jhet.322     Document Type: Article

References (28)

1. Dandia, A.; Arya, K.; Sati, M.; Sarawgi, P. J Fluorine Chem 2004, 125, 1273.
2. Wang, X. S.; Zhang, M. M.; Zeng, Z. S.; Shi, D. Q.; Tu, S. J.; Wei, X. Y.; Zong, Z. M. Tetrahedron Lett 2005, 46, 7169.
3. Cho, C. S.; Kim, J. S.; Oh, B. H.; Kim, T. J.; Shim, S. C.; Yoon, N. S. Tetrahedron 2000, 56, 7747.
4. Khadilkar, B. M.; Gaikar, V. G.; Chitnavis, A. A. Tetrahedron Lett 1995, 36, 8083.
5. Cho, C. S.; Kim, J. H.; Shim, S. C. Tetrahedron Lett 2000, 41, 1811.
6. Totlani, V. M.; Peterson, D. G. J Agric Food Chem 2005, 53, 4130.
7. Wnorowski, A.; Yaylayan, V. A. J Agric Food Chem 2000, 48, 3549.
8. Bose, D. S.; Fatima, L.; Mereyala, H. B. J Org Chem 2003, 68, 587.
9. Bossert, F.; Meyer, H.; Wehinger, E. Angew Chem Int Ed Engl 1981, 20, 762.
10. Stou, D. M.; Meyers, A. I. Chem Rev 1982, 82, 223.
11. Chorvat, R. J.; Rorig, K. J. J Org Chem 1988, 53, 5779.
12. Goldmann, S.; Stoltefuss, J. Angew Chem Int Ed Engl 1991, 30, 1559.
13. Loev, B.; Goodman, M. M.; Snader, K. M.; Tedeschi, R.; Macko, E. J Med Chem 1974, 17, 956.
14. Schramm, M.; Thomas, G.; Tower, R.; Franckowiak, G. Nature 1983, 303, 535.
15. Shanmugasundaram, P.; Murugan, P.; Ramakrishnan, V. T.; Ramamurthy, P. Heteroat Chem 1996, 7, 17.
16. Timpe, H. J.; Ulrich, S.; Decker, C.; Forassier, J. P. Macormolecules 1993, 26, 4560.
17. Tu, S. J.; Li, T. J.; Zhang, Y.; Shi, F.; Xu J. N.; Wang, Q.; Zhang, J. P.; Zhu, X. T.; Jiang, B.; Jia, R. H.; Zhang, J. Y. J Heterocycl Chem 2007, 44, 83.
18. Wang, X. S.; Shi, D. Q.; Wang, S. H.; Tu, S. J. Chin J Org Chem 2003, 23, 1291.
19. Jin, T. S.; Zhang, J. S.; Guo, T. T.; Wang, A. Q.; Li, T. S. Synthesis 2004, 12, 2001.
20. Wang, X. S.; Zhang, M. M.; Shi, D. Q.; Tu, S. J.; Wei, X. Y.; Zong, Z. M. Synthesis 2006, 24, 4187.
21. Wang, G. W.; Miao, C. B. Green Chem 2006, 8, 1080.
22. The 12 principles are as follows: prevention, atom economy, less hazardous chemical synthesis, designing safer chemicals, safer solvents, design for energy efficiency, use of renewable feedstocks, reduce derivatives, catalysis, design for degradation, real-time analysis for pollution prevention, inherently safer chemistry for accident prevention.
23. Tang, Z. Q.; Cao, X. D.; Jiang, B.; Li, C. M.; Zhou, D. X. Acta Cryst 2007, E63, o3811.
24. Liu, Q. D.; Tang, Z. Q.; Du, X. H. Acta Cryst 2007, E63, o3924.
25. Chen, Y.; Hao, W. J.; Tang, Z. Q.; Jiang, B.; Li, C. M. Acta Cryst 2007, E63, o3934.
26. Tang, Z. Q.; Liu, C. N.; Hao, W. J.; Wu, S. S. Acta Cryst 2008, E64, o1844.
27. Shi, D. Q.; Ni, S. N.; Yang, F.; Shi, J. W.; Dou, G. L.; Li, X. Y.; Wang, X. S. J Heterocycl Chem 2008, 45, 653.
28. Chandrasekhar, S.; Rao, Y. S.; Sreelakshmi, L.; Mahipal, B.; Reddy, C. R. Synthesis 2008, 1737.