An efficient synthesis of 2,2-bis(1H-indol-3-yl)-2H-acenaphthen-1-one catalyzed by recyclable solid superacid SO42-/TiO2 under grinding condition

Chinese Chemical Letters

Volumn 21, Issue 9, 2010, Pages 1057-1061

  Feng, Guo Liang ^a  

^a HEBEI UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

2,2 Bis(1H indol 3 yl) 2H acenaphthen 1 one; Acenaphthenequinone; Indole; Solid superacid SO42 TiO2

Indexed keywords

EID: 77955050784     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2010.05.009     Document Type: Article

References (21)

1. Smith A.L., Stevenson G.I., Lewis S., et al. Bioorg. Med. Chem. Lett. 2000, 10:2693.
2. Liu Y., Gribble G.W. Tetrahedron Lett. 2000, 41:8717.
3. Glennon R.A. J. Med. Chem. 1997, 40:1.
4. Lounasmaa M., Tolvanen A. Nat. Prod. Rep. 2000, 17:175.
5. Hibino S., Chozi T. Nat. Prod. Rep. 2001, 18:66.
6. Zhang H.C., Ye H., Moretto A.F., et al. Org. Lett. 2000, 2:89.
7. Osawa T., Namiki M. Tetrahedron Lett. 1983, 24:4719.
8. Bifulco G., Bruno I., Riccio R. J. Nat. Prod. 1995, 58:1254.
9. Veluri R., Oka I., Wagner-Dobler I., et al. J. Nat. Prod. 2003, 66:1520.
10. Mahadevan A., Sard H., Gonzalez M., et al. Tetrahedron Lett. 2003, 44:4589.
11. Li J., Zhou M., Li B.G., et al. Synth. Commun. 2004, 34:275.
12. Bennasar M.L., Vidal B., Bosch J. J. Org. Chem. 1997, 62:3597.
13. Amat M., Hadida S., Pshenichnyi G., et al. J. Org. Chem. 1997, 62:3158.
14. Rainier J.D., Smith A.B. Tetrahedron Lett. 2000, 41:9419.
15. Kim K.N., Song K.C., Noh J.H., et al. Bull. Korean Chem. Soc. 2009, 30:197.
16. Wang S.Y., Ji S.J. Tetrahedron 2006, 62:1527.
17. Paira P.Y., Hazra A.H. Bioorg. Med. Chem. Lett. 2009, 19:4786.
18. Tanaka K., Toda F. Chem. Rev. 2000, 100:1025.
19. Ren Z.J., Cao W.G., Ding W.Y., Shi W. Synth. Commun. 2004, 34:4395.
20. Hino M., Arata K. J. Chem. Soc. Chem. Commun. 1979, 101:1148.
21. Hino M., Kobayashi S., Arata K. J. Am. Chem. Soc. 1979, 101:6439.