Synthesis of diindolylmethanes (DIMs) catalyzed by silicotungstic acid by grinding method

E-Journal of Chemistry

Volumn 7, Issue 3, 2010, Pages 922-926

  Li, Ji Tai ^a   Sun, Shao Feng ^a  

^a HEBEI UNIVERSITY   (China)

Author keywords

Catalysis; Diindolylmethanes; Grinding; Silicotungstic acid; Synthesis

Indexed keywords

EID: 77957353022     PISSN: None     EISSN: 09734945     Source Type: Journal    
DOI: 10.1155/2010/986980     Document Type: Article

References (47)

1. Jitendra R S, Kalpesh D P and Radha V J, Catal Commun., 2008, 9, 1071.
2. Javad A, Fatemeh T and Mohammad R M, Catal Commun., 2007, 8, 1117.
3. Nagarajan R and Perumal P T, Tetrahedron, 2002, 5, 1229
4. Chen D, Yu L and Wang P G, Tetrahedron Lett., 1996, 37, 4467
5. Yadav J S, Reddy B V S, Murthy C V S R, Kumar G M and Madan C, Synthesis, 2001, 783
6. Rajitha B, Reddy P N and Kumar B S, J Chem Res Synop., 2005, 222
7. Mo L P, Ma Z C and Zhang Z H, Synth Commun., 2005, 1997
8. Sharma G V M, Reddy J J, Lakshmi P S and Krishna P R, Tetrahedron Lett., 2004, 45, 7729
9. Karthik M, Tripathi N M, Gupta N M, Palanichamy M and Murugesan V, Catal Commn., 2004, 5, 371
10. Reddy A V, Ravinder K, Reddy V L N, Goud T V, Ravikanth V and Venkateseswarlu Y, Synth Commun., 2003, 33, 3687
11. Singh P R, Singh D U and Samant S D, Synth Commun., 2005, 35, 2133
12. Palaniappan S and John A, J Mol Catal A: Chem., 2005, 242, 168
13. Wang L M, Han J W, Tian H, heng J, Fan Z Y and Tang X P, Synlett., 2005, 337
14. Zeng X F, Ji S J and Wang S Y, Tetrahedron, 2005, 61, 10235
15. Ramesh C, Banerjee J, Pal R and Das B, Adv Synth Catal., 2003b, 345, 557
16. Chakrabarty M, Ghosh N, Basak R and Harigaya Y, Tetrahedron, 2002, 43, 4075.
17. Li J T, Dai H G, Xu W Z and Li T S, Ultrason Sonochem., 2006, 13, 24.
18. Ji S J, Wang S Y, Zhang Y and Loh T P, Tetrahedron, 2004, 60, 2051
19. Bandgar B P and Shaikh K A, Tetrahedron Lett., 2003, 44, 1959
20. Selvam J J, Srinivasulu M, Suryakiran N, Suresh V, Reddy S M and Venkateswarlu Y, Synth Commun., 2008, 38, 1760
21. Khalafi-Nezhad A, Parhami A, Zare A, Zare A R M, Hasaninejad A and Panahi F, Synthesis, 2008, 4, 617
22. Hasaninejad A, Zare A, Sharghi H, Shekouhy M, Khalifeh R, Beni A S and Zare A R M, Can J Chem., 2007, 85, 416
23. Minoo D, Mostafa B, Seyedeh C A, Shaghayegh A A and Reza R A, Lett Org Chem., 2008, 5, 490.
24. Pasha M A and Jayashankara V P, J Pharmacol Toxicol., 2006, 1, 585.
25. Bandgar B P, Abasaheb, Patil V and Kamble V T, ARKIVOC, 2007, 16, 252.
26. Alireza H, Abdolkarim Z, Hashem S, Khodabakhsh N and Mohsen S, ARKIVOC, 2007, 14, 39.
27. Minoo D, Peyman S, Mostafa B, Yasamin V and Shadi K, Monatsh Chem., 2007, 138, 595.
28. Mona H S, Synth Commun., 2008, 38, 832
29. Li J T and Lin Z P, Chin J Org Chem., 2008, 28, 1238.
30. Nadkarni S V, Gawande M B, Jayaram R V and Nagarkar J M, Catal Commun., 2008, 9, 1728.
31. Heravi M M, Ranjbar L, Derikvand F and Bamoharram F F, Catal Commun., 2007, 8, 289.
32. Murugan R and Reddy B S R, Tetrahetron., 2005, 61, 12275.
33. Okuhara T, Mi zuno N and Misono M, Appl Catal., A, 2001, 222, 63
34. Misono M, Catal Rev., 1987, 29, 269.
35. Nagahara H, Kagawa H, Kagawa K, Iwaisako T and Komaki H, Angew Chem Int Ed., 2000, 9, 2102.
36. Lou Y M and Bai A M, Sci Tech Chem Indus., 2003, 11, 49.
37. Ouyang Y Z, Zou X Y and Peng Q J, J Jishou Univ (Nat. Sci. Ed.), 2000, 21, 53.
38. Kamakshi R and Reddy B S R, Catal Commun., 2007, 8, 825.
39. Li J T and Sun M X, Aust J Chem., 2009, 62, 353.
40. Geng L J, Li J T and Wang S X, Chin J Org Chem., 2005, 25, 608
41. Geng L J, Wang S X, Li J T and Liu C H, Chin J Org Chem., 2002, 22, 1047
42. Li J T, Dai H G, Liu D and Li T S, Synth Commun., 2006, 36, 789.
43. Wang S X, Li J T, Yin Y H and Zhang Y, J Hebei Univ (Nat Sci Ed.,), 2003, 23, 385.
44. Wang S X, Li J T and Wang Z H, Chin J Org Chem., 2004, 24, 447.
45. Feng X L, Guan C J and Zhao C X, Synth Commun., 2004, 34, 487.
46. Bergman J, J Heterocycl Chem., 1970, 7, 1071.
47. Bandgar B P, Bettiger S V and Joshi N S, Monatsh Chem., 2004, 10, 1265.