One-pot preparation of coumarins by Knoevenagel condensation in solvent-free condition under microwave irradiation

Heterocyclic Communications

Volumn 7, Issue 1, 2001, Pages 67-72

  Balalaie, Saeed ^a   Nemati, Navid ^a  

^a K N TOOSI UNIVERSITY OF TECHNOLOGY   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0035589374     PISSN: 07930283     EISSN: None     Source Type: Journal    
DOI: 10.1515/HC.2001.7.1.67     Document Type: Article

References (36)

1. R. O'Kennedy and R. D. Thornes; Coumarins, John Wiley & Sons Ltd, New York, 1997, pp. 1-267.
2. (a) R. S. Mali S., N. Yeola and B. K. Kulkarni, Indian J. Chem., 22 B, 352 (1983).
3. (b) L. A. Singer and N. P. Kong, J. Am. Chem. Soc. 88, 5213 (1966).
4. (c) N. S. Narasimhan, R. S. Mali and M. V. Barve; Synthesis, 906 (1979).
5. (a) J. D. Kendal, H. R. J. Waddington and G. F. Duffin; Chem. Abstr., 55, 21927 (1961).
6. (b) P. Loew (Ciba-Geigh A.-G.); Chem. Abstr. 87, 18608 (1977).
7. (c) H. Hagen and R. D. Kohler (BASF A.-G.); Chem. Abstr, 95, 187261 (1981).
8. (d) R. Rane, H. Harnish and K. H. Drexhage; Heterocycles, 21, 167 (1984).
9. (a) A. Hammand, A. S. El-Sayed, I. E. Islam and N. Shafik; J. Chem. Soc. Pak.; 12, 292 (1990).
10. (b) G. M. Kulkarni, H. V. Kulkarni, V. D. Patil, D. B. Shridhar and M. Laxmana; Rev. Roum. Chim, 35, 549 (1990).
11. (c) R. G. Harvey, C. Cortex, T. P. Ananthanarayan and S. Schmolka; J. Org. Chem. 53, 3936 (1988).
12. L. Tietze and V. Beifuss; Comprehensive Organic Synthesis (Eds.: B. M. Trost, I, Fleming), Pergamon Press, Oxford, Vol II, 341 (1991).
13. J. R. Johnson; Org. React. 1, 210 (1942).
14. (a) S. Sethna and R. Padke; Org. React., 7, 1 (1953).
15. (b) Tong-Shuang Li, Zhan-Hui Zhang, Feng Yang and Cheng-Guang Fu; J. Chem. Research(s), , 38 (1998).
16. (a) G. Jones; Organic React., 15, 204 (1967).
17. (b) Gianluca Brufola, Francesco Fringuelli, Oriano Piermatti and Ferdinando Pizzo; Heterocycles, 43, 1257 (1996).
18. R. L. Shirner; Org. React. 1, 1 (1942).
19. I. Yavari, R. Hekmat-Shoar and A. Zonouzi; Tetrahedron Letters, 39, 2391 (1998).
20. (a) R. A. Abramovich; Org Prep. Proced. Int. 23, 683 (1991).
21. (b) D. M. P. Mingos and D. R. Baghurst; Chem. Soc. Rev. 20, 1 (1991).
22. (c) S. Caddick; Tetrahedron, 51, 10403 (1995).
23. (d) C. R. Strauss and R.W. Trainer; Aust. J. Chem. 48, 1665 (1995).
24. (e) A. Loupy, A. Petit, J. Hamelin, F. Texier-Boullet, P. Jacquault and D. Mathe; Synthesis, 1213 (1998).
25. (f) R. S. Varma, Green Chem., 1, 43 (1999).
26. (g) R. S. Varma; Clean Products and Processes, 1, 132 (1999).
27. S. Balalaie and N. Nemati; Synthetic Commun., 30, 869 (2000).
28. A. Ramani, B. M. Chanda, S. Velu and S. Sivasanker; Green Chem., 1, 163 (1999).
29. B. P. Bandgar, L. S. Uppalla and D. S. Kurule; Green Chem., 1, 243 (1999).
30. E.C Horning, M.G. Horning and D. A Dimming; Org. Synthesis; Coll. Vol III, 165 (1955).
31. (a) A. K. Bose, M. S. Manhas, M. Gosh, V. S. Raju, K. Tabei and Z. Urbanczyk-Lipkowska; Heterocycles, 30, 741 (1990).
32. (b) R. N. Gedye, J. B. Wei, Can J. Chem., 76, 525 (1998).
33. (c) D. Bogdal, J.; Chem. Res.(s), 468 (1998).
34. Beilstein; Handbuch der Organischen Chemie, Band 18, I, 493.
35. N. P. Buu-Hoi, T. B. Loc and N. D. Xuong; Bull. Soc. Chim. France, 561 (1957).
36. H. Yasuda and H. Midorikawa; Bull. Chem. Soc. Japan, 39, 1754 (1966)