One-pot synthesis of quinaldine derivatives by using microwave irradiation without any solvent - A green chemistry approach

Journal of Chemical Sciences

Volumn 121, Issue 4, 2009, Pages 481-484

  Safari, Javad ^a   Banitaba, Sayed Hossein ^a   Samiei, Sepehr Sadegh ^a  

^a UNIVERSITY OF KASHAN   (Iran)

Author keywords

Br nsted acid; Green chemistry; Microwave irradiation; One pot; Quinaldine; Solvent free

Indexed keywords

ALUMINA; BROMINE; IRRADIATION; SOLVENTS;

ANILINE DERIVATIVES; GREEN CHEMISTRY; GREEN CHEMISTRY APPROACHES; ONE POT; ONE-POT REACTION; ONE-POT SYNTHESIS; QUINALDINE; SOLVENT FREE;

MICROWAVE IRRADIATION;

EID: 68749090938     PISSN: 09743626     EISSN: 09737103     Source Type: Journal    
DOI: 10.1007/s12039-009-0057-0     Document Type: Article

References (27)

1. Elguero J. 1984 Comprehensive heterocyclic chemistry. (ed.) A McKillop (Oxford: Pergamon Press) Vol. 5, p. 167
2. Penning T. D. Talley J. J. Bertenshaw S. R. Carter J. S. Colins P. W. Graneton J. M. Lee L. F. and Malecha J. W. 1997 J. Med. Chem. 40 1347
3. Menozzi G. Mosti L. Fossa P. Maltioli F. and Ghia M. 1997 J. Heterocycl. Chem. 34 963
4. Naik R. D. and Desai K. R. 1998 Orient. J. Chem. 14 161
5. Kidwai M. and Negi N. 1997 Monatsh. Chem. 128 85
6. El-Sayed O. A. El-Bieh F. B. El-Aqeel S. I. Al-Bassam B. A. and Hussein M. E. 2002 Bull. Chim. Farm. 141 461
7. Selvi S. T. Nadaraj V. Mohan S. Sasi R. and Hema M. 2006 Bioorg. Ed. Chem. 14 3896
8. Jashi A. A. Narkhede S. S. and Viswanathan C. L. 2005 Bioorg. Med. Chem. Lett. 15 73
9. Suresh T. Nandha Kumar R. Magesh S. and Mohan P. S. 2003 Indian J. Chem. B42 2133
10. Suresh T. Nandha Kumar R. Magesh S. and Mohan P. S. 2003 Indian J. Chem. B42 688
11. Skraup H. 1880 Chem. Ber. 13 2086
12. Doebner O. and Miller W. 1883 Bericht. 16 2464
13. Friedlander P. 1882 Chem. Ber. 15 2572
14. Hall N. 1994 Science 266 32
15. (a) Loupy A. Petit A. Hamelin J. Texier-Boullet F. Jacquault P. and Mathe D. 1998 Synthesis 2113;
16. (b) Perreux L. and Loupy A. 2001 Tetrahedron 57 9199;
17. (c) Lindstroem P. Tierney J. Wathey B. and Westman J. 2001 Tetrahedron 57 9225;
18. (d) Varma R. S. 1999 Green Chem. 43
19. (a) Kim J. K. Kwon P. S. Kwon T. W. Chung S. K. and Lee J. W. 1996 Synth. Commun. 26 535;
20. (b) Kim S. Y. Kwon P. S. Kwon T. W. Chung S. K. and Chang Y. T. 1997 Synth. Commun. 27 533
21. (c) Kwon P. S. Kim Y. S. Kang C. J. Kwon T. W. Chung S. K. and Chang Y. T. 1997 Synth. Commun. 27 4091
22. (a) Manske R. H. F. 1942 Can. J. 20 133;
23. (b) Minkin V. I. 1961 Chem. Abs. 55 14457;
24. (c) Hamer F. M. 1921 J. Chem. Soc. 119 1432;
25. (d) Neumann M. 1946 Org. Synth. 26 47;
26. (e) Buu-Hoi N. P. 1948 J. Chem. Soc. 106 110
27. Denmark S. E. and Venkatraman S. 2006 J. Org. Chem. 71 1668