Sulfonic acid functionalized mesoporous SBA-15 for one-pot synthesis of substituted aryl-14H-dibenzo xanthenes and bis(indolyl) methanes

Catalysis Communications

Volumn 11, Issue 14, 2010, Pages 1148-1153

  Naik, Mallari A ^a   Sachdev, Divya ^a   Dubey, Amit ^a  

^a BIRLA INSTITUTE OF TECHNOLOGY AND SCIENCE   (India)

Author keywords

Bis (indolyl) methanes; Heterogeneous catalysis; SBA 15; Xanthenes

Indexed keywords

BIS(INDOLYL)METHANES; CATALYTIC ACTIVITY; CATALYTIC PERFORMANCE; CHARACTERIZATION TECHNIQUES; ENVIRONMENTALLY BENIGN; FTIR; FUNCTIONALIZED SBA-15; HETEROGENEOUS CATALYSIS; HIGH YIELD; MESOPOROUS SBA-15; ONE-POT SYNTHESIS; POWDER X RAY DIFFRACTION; SULFONIC ACID-FUNCTIONALIZED;

ACIDS; CATALYSIS; CATALYST ACTIVITY; IONIC LIQUIDS; TEMPERATURE PROGRAMMED DESORPTION; X RAY DIFFRACTION;

METHANE;

EID: 77954548908     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2010.06.004     Document Type: Article

References (29)

1. R.A. Sheldon, M. Wallau, I.W.C.E. Arends, and U. Schuchardt Acc. Chem. Res. 31 1998 485
2. T. Hideo Jpn. Tokkyo Koho JP 56005480 1981
3. J.P. Poupelin, G. Saint-Ruf, O. Foussard-Blanpin, G. Narcisse, G. Uchida-Ernouf, and R. Lacroix Eur. J. Med. Chem. 13 1978 67
4. R.W. Lambert, J.A. Martin, J.H. Merrett, K.E.B. Parkes, and G.J. Thomas PCT Int. Appl. WO 9706178 1997 212377
5. A. Banerjee, and A.K. Mukherjee Stain Technol. 56 1981 83
6. S.M. Menchen, S.C. Benson, J.Y.L. Lam, W. Zhen, D. Sun, B.B. Rosenblum, S.H. Khan, M. Taing, US 2003.
7. A. Bekaet, J. Andrieux, and M. Plat Tetrahedron Lett. 33 1992 2805
8. R. Sarma, and J. Baruah Dyes Pigm. 64 2005 91
9. C.A. Buehler, D.E. Cooper, and E.O. Srudder J. Org. Chem. 8 1943 316
10. J.Q. Wang, and R.G. Harvey Tetrahedron 58 2002 5927
11. D.W. Knight, and P.B. Little J. Chem. Soc., Perkin Trans. 2001 2001 1771
12. B. Rajitha, B. Sunil Kumar, Y. Thirupathi Reddy, P. Narsimha Reddy, and N. Sreenivasulu Tetrahedron Lett. 46 2005 8691
13. S. Ko, and C. Yao Tetrahedron Lett. 47 2006 8827
14. M.A. Pasha, and V.P. Jayashankara Bioorg. Med. Chem. Lett. 17 2007 621
15. M. Dabiri, M. Baghbanzadeh, M.S. Nikcheh, and E. Arzroomchilar Bioorg. Med. Chem. Lett. 18 2008 436
16. B.B.F. Mirjalili, A. Bamoniri, and A. Akbari Tetrahedron Lett. 49 2008 6454
17. K. Venkatesan, S.S. Pujari, R.J. Lahoti, and K.V. Srinivasan Ultrason. Sonochem. 15 2008 548
18. S. Rostamizadeh, N. Shadjou, A.M. Amani, and S. Balalaie Chin. Chem. Lett. 19 2008 1151
19. W. Su, D. Yang, C. Jin, and B. Zhang Tetrahedron Lett. 49 2008 3391
20. M. Chakrabarty, N. Ghosh, R. Basak, and Y. Harigaya Tetrahedron Lett. 43 2002 4075
21. R. Bell, S. Carmeli, and N. Sar J. Nat. Prod. 57 1994 1587
22. R. Sundberg The Chemistry of Indoles 1970 Academic Press
23. H. Shaterian, M. Ghashang, and A. Hassankhani Dyes Pigm. 76 2008 564
24. M. Seyyedhamzeh, P. Mirzaei, and A. Bazgir Dyes Pigm. 76 2008 836
25. Q. Yang, M.P. Kapoor, and S. Inagaki J. Am. Chem. Soc. 124 2002 9694
26. M.E. Davis Nature 417 2002 813
27. C.T. Kresge, M.E. Leonowicz, W.J. Roth, J.C. Vartuli, and J.S. Beck Nature 359 1992 710
28. Z.H. Zhang, L. Yin, and Y.M. Wang Synthesis 2005 1949
29. B. Bandgar, and K. Shaikh Tetrahedron Lett. 44 2003 1959