Ferric nitrate nonahydrate as a mild and efficient catalyst for the synthesis of ß-enaminones

Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry

Volumn 53, Issue 8, 2014, Pages 1122-1127

  Khajuria, Rajni ^a   Ambica, A ^a   Saini, Yeshwinder ^a   Kapoor, Kamal K ^a  

^a UNIVERSITY OF JAMMU   (India)

Author keywords

Amines; Ferric nitrate nonahydrate; enaminones; dicarbonyl compounds

Indexed keywords

EID: 84906736936     PISSN: 03764699     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (31)

1. The Chemistry of Enamines I, edited by Z Rappoport (John Wiley & Sons, New York), 1994
2. Eddington N D, Cox D S, Roberts R R, Stables J P, Powell C B & Scott K R, Curr Med Chem, 7, 2000, 417
3. Alan C, Spivey A C, Srikaran R, Diaper C M, David J & Turner D, Org Biomol Chem, 1, 2003, 1638
4. Hassneen H M & Abdallah T A, Molecules, 8, 2003, 333;
5. Michael J P, Koning C B, Gravestock D, Hosken G D, Howard A S, Jungmann C M, Krause R W M, Parsons A S, Pelly S C & Stanbury T V, Pure Appl Chem, 71, 1999, 979
6. Cimarelli C & Palmieri G, J Org Chem, 61, 1996, 5557
7. Bartoli G, Cimarelli C, Marcantoni E, Palmieri G & Petrini M, J Org Chem, 59, 1994, 5328
8. Beholz L G, Benovsky P, Ward D L & Barta N S, J Org Chem, 62, 1996, 1033
9. David O, Blot J, Bellec C, Fargeau-Bellassoued M C, Haviari G, Celerier J P, Lhommet G, Gramain J C & Gardette O, J Org Chem, 64, 1999, 3122
10. Sweeney T R & Strube R E, in Burger's Medicinal Chemistry II, edited M E Wolff (Wiley, NewYork), 1979, p. 333
11. Foster J E, Nicholson J M, Butcher R, Stables J P, Edafiogho I O, Goodwin A M, Henson M C, Smith C A & Scott K R, Bioorg Med Chem, 7, 1999, 2415;
12. Edafiogho I O, Moore J A, Alexander M S & Scott K R, J Pharm Sci, 83, 1994, 1155
13. Dane E, Drees F, Konrad P & Dockner T, Angew Chem, 74, 1962, 873
14. Baraldi P G, Simoni D & Manfredini S, Synthesis, 1983, 902;
15. Martin D F, Janusonis G A & Martin B B, J Am Chem Soc, 83, 1961, 73
16. Rechsteiner B, Texier-Boullet F & Hamelin J, Tetrahedron Lett, 34, 1993, 5071
17. Valduga C J, Squizani A, Braibante H S & Braibante M E F, Synthesis, 10, 1998, 1019
18. Arcadi A, Bianchi G, Di Giuseppe S & Marinelli F, Green Chem, 5, 2003, 64
19. Stefani H A, Costa I M & Silva D O, Synthesis, 12, 2000, 1526
20. Bhatte K D, Tambade P J, Dhake K P & Bhanage B M, Catal Commun, 11, 2010, 1233
21. Rafiee E, Mahdavi H, Eavani S, Joshaghane M & Shiri F, Appl Catal A: Gen, 352, 2009, 202
22. Adude R N, Tigote R M & Bhusare S R, Der Chemica Sinica, 3, 2012, 231
23. Epifano F, Genovese S & Curini M, Tetrahedron Lett, 48, 2007, 2717
24. Gholap A R, Chakor N S, Daniel T, Lahoti R J & Srinivasan K V J, Mol Catal A: Chem, 245, 2006, 37
25. Eshghi H, Seyedi S M, Safaei E, Vakili M, Farhadipour A & Bayat-Mokhtari M, J Mol Catal A: Chem, 363, 2012, 430
26. Cui B, Wang R H, Chen L Z, Jin Y & Han G F, Synth Commun, 41, 2011, 1064
27. Koduri N D, Scott H, Hileman B, Cox J D, Coffin M, Glicksberg L & Hussaini S R, Org Lett, 14, 2012, 440
28. Firouzabadi H, Iranpoor N & Amani K, Synthesis, 15, 2003, 408
29. Ambica, Kumar S, Taneja S C, Hundal M S & Kapoor K K, Tetrahedron Lett, 49, 2008, 2208;
30. Mahajan D, Naqvi T, Sharma R L & Kapoor K K, Aus J Chem, 61, 2008, 159;
31. Verma A K, Koul S, Kapoor K K & Razdan T K, Aus J Chem, 60, 2007, 883.