Enamination of 1,3-dicarbonyl compounds catalyzed by tin tetrachloride

Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry

Volumn 46, Issue 3, 2007, Pages 535-539

  Zhang, Zhan Hui ^a   Ma, Zi Chuan ^a   Mo, Li Ping ^a  

^a HEBEI NORMAL UNIVERSITY   (China)

Author keywords

diketones; enaminones; ketoesters; Amines; Tin tetrachloride

Indexed keywords

EID: 34548259217     PISSN: 03764699     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (43)

1. Rappoport Z, The Chemistry of Enamines, Part 1, (John Wiley & Sons, New York), 1994.
2. Greenhill J V, Chem Soc Rev, 6, 1977, 277.
3. Elassar A-Z A & El-Khair A A, Tetrahedron, 59, 2003, 8463.
4. Michael J P, De 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.
5. Ferraz H M C & Pereira F L C, Quimica Nova, 27, 2004, 89.
6. Hannick S M & Kishi Y, J Org Chem, 48, 1983, 3833.
7. Jiang N, Qu Z & Wang J, Org Lett, 3, 2001, 2989.
8. Katritzky A R, Fang Y, Donkor A & Xu J, Synthesis, 2000, 2029.
9. Fustero S, García del la Torre M, Jofrè V, Pérez Carlon R, Navarro A & Simón Fuentes A, J Org Chem, 63, 1998, 8825.
10. Baraldi P G, Simoni D & Manfredini S, Synthesis, 1983, 902.
11. Potěšil T, J Chromatogr, 312, 1984, 387.
12. Cone E J, Garner R H & Hayes A W, J Org Chem, 26, 1972, 4436.
13. Saeed A A H, J Chem Eng Data, 29, 1984, 358.
14. Martin D F, Janusonis G A & Martin B B, J Am Chem Soc, 83, 1961, 73.
15. Yapi A D, Mustofa M, Valentin A, Chavignon O, Teulade J-C, Mallie M, Chapat J-P, Blache Y, Chem Pharm Bull, 48, 2000, 1886.
16. Brandt C A, Da Silva ACMP, Pancote C G, Brito C L & Da Silveira M A B, Synthesis, 2004, 1557.
17. Cartaya-Marin C P, Henderson D G & Soeder R W, Synth Commun, 27, 1997, 4275.
18. Rechsteimer B, Texier-Boullet F & Hamelin J, Tetrahedron Lett, 34, 1993, 5071.
19. Valduga C J, Squizani A, Braibante H S & Braibante M E F, Synthesis, 1998, 1019.
20. Stefane B & Polanc S, Synlett, 2004, 698.
21. Texier-Bouliet F, Synthesis, 1985, 679.
22. Gao Y-H, Zhang Q-H & Xu J-X, Synth Commun, 34, 2004, 909.
23. Bartoli G, Bosco M, Locatelli M, Marcantoni E, Melchiorre P & Sambri L, Synlett, 2004, 239.
24. Khodaei M M, Khosropour A R & Kookhazadeh M, Synlett, 2004, 1980.
25. Arcadi A, Bianchi G, Di Giuseppe S & Marinelli F, Green Chem, 5, 2003, 64.
26. Khosropour A R, Khodaei M M & Kookhazadeh M, Tetrahedron Lett, 45, 2004, 1725.
27. Silva F C, De Souza M C B V, Ferreira V F, Sabino S J & Antunes O A C, Catal Commun, 5, 2004, 151.
28. Stefani H A, Costa I M, De O Silva D, Synthesis, 2000, 1526.
29. Ogata T, Okamoto I, Doi H, Kotani E & Takeya T, Tetrahedron Lett, 44, 2003, 2041.
30. Dussault P H & Liu X, Tetrahedron Lett, 40, 1999, 6553.
31. Kanemasa S, Kanai T, Araki T & Wada E, Tetrahedron Lett, 40, 1999, 5055.
32. Pathak A K, EI-Kattan Y A, Bansal N, Maddry J A & Reynolds R C, Tetrahedron Lett, 39, 1998, 1497.
33. Miel H & Rault S, Tetrahedron Lett, 38, 1997, 7865.
34. Peng S & Qing F-L, J Fluorine Chem, 103, 2000, 135.
35. Hayashi Y & Sasaki Y, Chem Commun, 2005, 2716.
36. Fuchibe K, Aoki Y & Akiyama T, Chem Lett, 34, 2005, 538.
37. O'Neill P M, Rawe S L, Storr R C, Ward S A & Posner G H, Tetrahedron Lett, 46, 2005, 3029.
38. Zhang Z-H, J Chem Res, 2004, 753.
39. Zhang Z-H, Monatsh Chem, 136, 2005, 1191.
40. Mo L-P, Ma Z-C & Zhang Z-H, Synth Commun, 35, 2005, 1997.
41. Zhang Z-H & Song L-M, J Chem Res, 2005, 817.
42. Zhang Z-H, Yao S-T & Lin J, Synth Commun, 36, 2006, 1645.
43. Cui Z-S, Zhang Z-H & Liu S-F, J Chem Res, 2006, 390.