A simple synthesis of enaminones from reaction between isocyanides and cyclic 1,3-dicarbonyl compounds

Journal of Chemical Research

Volumn , Issue 4, 2008, Pages 198-200

  Maghsoodlou, Malek Taher ^a   Hazeri, Nourallah ^a   Habibi Khorassani, Sayyed Mostafa ^a   Solimani, Vahideh ^a   Marandi, Ghasem ^a   Razmjoo, Zahra ^a  

^a UNIVERSITY OF SISTAN AND BALUCHESTAN   (Iran)

Author keywords

1,3 dicarbonyl compounds; Enaminones; Isocyanides; Pull push olefins; Pyrimidinones

Indexed keywords

EID: 56049113439     PISSN: 03082342     EISSN: None     Source Type: Journal    
DOI: 10.3184/030823408X314482     Document Type: Article

References (32)

1. I. Ugi, Isonitrile chemistry, Academic Press, London, 1971.
2. I. Ugi, Angew, Chem, Int. Ed. Engl., 1982, 21, 810.
3. S. Marcaccini and T. Torroba, Org. Prep. Proced. Int., 1993, 25, 141.
4. H.M. Walborsky and M.P. Persiasamy, in The chemistry of functional groups, Suppl. C, eds. S. Patai and Z. Rappoport, Wiley, New York, 1983.
5. I. Yavari, N. Hazeri, M.T. Maghsoodlou and A. Moradi, J. Chem. Res. (S)., 2001, 272.
6. I. Yavari and M.T. Maghsoodlou, J. Chem. Res. (S), 1998, 7, 386.
7. M.T. Maghsoodlou, N. Hazeri, H. Navvabian, Z. Razmjoo and G. Marandi, J. Chem. Res. (S), 2005, 14, 401.
8. M.T. Maghsoodlou, I. Yavari, F. Nassiri, H. Djahaniani and Z. Razmjoo, Monatsh. Chem., 2003, 134, 1585.
9. M.T. Maghsoodlou, N. Hazeri, S.M. Habibi-khorassani, G. Marandi and M. Nassiri, Synth. Commun., 2005, 35, 2771.
10. M.T. Maghsoodlou, N. Hazeri, S.M. Habibi-khorassani, R. Heydari, G. Marandi and M. Nassiri, Synth. Commun., 2005, 35, 2569.
11. M.T. Maghsoodlou, N. Hazeri, S.M. Habibi-khorassani, G. Marandi and M. Nassiri, J. Heterocyclic Chem., 2006, 43, 481.
12. Z. Rappoport, (ed.), The Chemistry of Enamines, Wiley, New York, 1994.
13. J.V. Greenhill, Chem. Soc. Rev., 197, 6, 277.
14. H. Bundgaard (ed), Design of prodrugs, Elsevier, Amsterdam, 1985, pp. 1.
15. I.O. Edafiogho, C.N. Hinko, H. Chang, J.A. Moore, D. Mulzac, J.M. Nicholson and K.R. Scott, J. Med. Chem., 1992, 35, 2798.
16. J.V. Greenhill, Chem. Soc. Rev., 1997, 6, 277.
17. I.O. Edafiogho, M.S. Alexander, J.A. Moore, V.A. Farrar and K.R. Scott, Curr. Med. Chem., 1994, 1, 159.
18. P. Lue and J.V. Greenhill, Adv. Heterocycl. Chem., 1996, 67, 207.
19. O.A. Atanasi, G. Favi, P. Filippone, B. Stanvnik and J. Svete, Synlett., 2003, 995.
20. L. Selic and B. Stanovnik, Helv. Chim. Acta., 1998, 81, 1634.
21. G. Menozzi, P. Schenone and L. Mosti, J. Heterocycl. Chem., 1983, 20, 645.
22. P. Schenone, P. Fossa and G. Menozzi, J. Heterocycl. Chem., 1991, 28, 453.
23. S. Zupncic. J. Svete and B. Stanovnik, Heterocycles., 2000, 53, 2033.
24. L. Pizzioli, B. Ornik, J. Svete and B. Stanovnik, Helv. Chim. Acta., 1998, 81, 231.
25. E.J. Breaux and K.E. Zwikelmaier, J. Heterocycl. Chem., 1981, 18, 183.
26. P. Schenone, L. Mosti and G. Menozzi, J. Heterocycl. Chem., 1982, 19, 1355.
27. J.R. Beck and M.P. Lynch, J. Heterocycl. Chem., 987, 24, 693.
28. B. Stanovnik and J. Svete, Targets Heterocycl. Syst., 2000, 4, 105.
29. J. Svete, J. Heterocycl. Chem., 2002, 39, 437.
30. J.W. Clark-Lewis and M.J. Thompson, J. Chem. Soc., 1959, 2401.
31. H. Bredereck, R. Gompper, F. Effenberger, K.H. Popp and G. Simchen, Chem. Ber., 1961, 94, 1241.
32. M. Sekiya and C. Yanahara, Chem. Pharm. Bull. (Tokyo), 1969, 17, 810.