An efficient, inexpensive 'Green Chemistry' route to multicomponent Biginelli condensation catalyzed by CuCl2.2H2O-HCl

Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry

Volumn 47, Issue 3, 2008, Pages 434-438

  Pathak, Vijai Nath ^a   Gupta, Ragini ^b   Varshney, Bindu ^a  

^a UNIVERSITY OF RAJASTHAN   (India)

^b MALAVIYA NATIONAL INSTITUTE OF TECHNOLOGY   (India)

Author keywords

Biginelli condensation; CuCl2.2H2O Conc. HCl; Dihydropyrimidinones; Green chemistry; Grindstone chemistry; Solvent free

Indexed keywords

EID: 42249116048     PISSN: 03764699     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (34)

1. Toda F, Tanaka K & Sekikawa A, J Chem Soc. Chem Commun, 1987, 279.
2. Bose A K, Pednekar S, Ganguly S N, Chakraborty G & Manhas S M, Tetrahedron Lett, 45, 2004, 8351.
3. Kappe C O, Kumar D & Varma R S, Synthesis, 1999, 1799.
4. Hentrich W & Schepss W (I. G. Farbenindustrie) DRP 1930, 547, 057; Forisch Teerfarbenfabr Verw Industriezweige; edited by Friedlander E 25, 1932, 2590.
5. Hull R (ICI Ltd.) Brit Patent 1965, 984, 365;
6. Chem Abstr, 62, 1965, 13159f.
7. Hurst E W & Hull R, J Med Pharm Chem, 3, 1961, 215.
8. Hurst E W, Ann N Y Acad Sci, 98, 1962, 275.
9. Patil A D, Kumar N V, Kokke W C, Bean M F, Freyer A J, DeBrosse C, Mai S, Truneh A, Faulkner D J, Carte B, Breen A L, Hertzberg R P, Johnson R K, Westley J W & Potts B C M, J Org Chem, 60, 1995, 1182.
10. Parlato M C, Mugnaini C, Renzulli M L, Corelli F & Botta M, Arkivoc, 5, 2004, 349.
11. (a) Atwal K S, Rovnyak G C, O' Reilly B C & Schwartz J, J Org Chem, 54, 1989, 5898;
12. (b) Kappe C O, Fabian W M F & Semones M A, Tetrahedron, 53, 1997, 2803.
13. Ranu B C, Hajra A & Jana U, J Org Chem, 65, 2000, 6270.
14. Partha P B, Sunil G, Dipak P & Jagir S S, Chem Lett, 10, 2002, 1038.
15. Sabitha G, Kiran Kumar Reddy G S, Srinivas Reddy Ch & Yadav J S, Synlett, 2003, 858.
16. Lu J, Bai Y, Wang Z, Yang B & Ma H, Tetrahedron Lett, 41, 2000, 9075.
17. Subhas Bose D, Fatima Liyakat & Hari Babu M, J Org Chem, 68, 2003, 587.
18. Kumar K A, Kasthuraiah M, Reddy C S & Reddy C D, Tetrahedron Lett, 42, 2001, 7873.
19. Martins A P M, Teixeira M V M, Cunico W, Scapin E, Mayer R, Pereira C M P, Zanatta N, Bonacorso H G, Peppe C & Yuan Y-F, Tetrahedron Lett, 45, 2004, 8991.
20. Lu J & Ma H, Synlett, 1, 2000, 63.
21. Ma Y, Qian C, Wang L & Yang M, J Org Chem, 65, 2000, 3864.
22. Bhosale R S, Bhosale S V, Bhosale S V, Wang T & Zubaidha P K, Tetrahedron Lett, 45, 2004, 9111.
23. Xue S, Shen Y C, Li Y L, Shen X M & Guo Q X, Chin J Chem, 20, 2002, 385.
24. Nareaiah AV, Basak A K & Nagaiah K, Synthesis, 8, 2004, 1253.
25. Balalaie S, Arabanian A & Hashtroudi M S, Monatshefte fur Chemie, 131, 2000, 945.
26. Kappe C O, Acc Chem Res, 33, 2000, 879.
27. Kappe C O, J Org Chem, 62, 1997, 7201.
28. Sun Q, Wang Y-Q, Ge Z-M, Cheng T-M & Li R-T, Synthesis, 7, 2004, 1047.
29. Hu E H, Sidler D R & Dolling U H, J Org Chem, 63, 1998, 3454.
30. Afzal Md P & Jayshankar V P, Indian J Heterocyclic Chemislry, 14, 2005, 261.
31. Zhu Yulin, Pan Yuanjiang & Huang Shenlin, Synth Commun, 34, 2004, 3167.
32. Wang Ji-Tao & Peppe Clovis, Tetrahedron, 58, 2002, 4801.
33. Singh K, Singh J, Deb Prasant K & Singh H, Tertrahedron, 55, 1999, 12873.
34. Bozsing D, Sohar P, Gigler G & Kovacs G, Eur J Med Chem Chim Ther, 31, 1996, 663.