Immobilized palladium metal containing ionic liquid catalyzed one step synthesis of isoindole-1,3-diones by carbonylative cyclization reaction

Journal of Molecular Catalysis A: Chemical

Volumn 385, Issue , 2014, Pages 91-97

  Khedkar, Mayur V ^a   Shinde, Ajinkya R ^a   Sasaki, Takehiko ^b   Bhanage, Bhalchandra M ^a  

^a INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

^b UNIVERSITY OF TOKYO   (Japan)

Author keywords

Carbonylation reaction; Heterogeneous catalysis; Immobilization; Palladium; Phosphine free

Indexed keywords

EID: 84894479781     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2014.01.018     Document Type: Article

References (30)

1. H.M. Colquhoun, D.J. Thompson, and M.V. Twigg Carbonylation, Direct Synthesis of Carbonyl Compounds 1991 Plenum Press New York
2. R. Skoda-Foldes, and L. Kollar Curr. Org. Chem. 6 2002 1097 1119
3. S.T. Gadge, and B.M. Bhanage RSC Adv. 2013 10.1039/C3RA46273K (in press)
4. R.A. Abramovitch, I. Shinkai, B.J. Mavunkel, K.M. More, S. O'Connor, G.H. Ooi, W.T. Pennington, P.C. Srinivasan, and J.R. Stowers Tetrahedron 52 1996 3339 3354
5. J.L. Wood, B.M. Stoltz, and S.N. Goodman J. Am. Chem. Soc. 118 1996 10656 10657
6. I.H. Hall, J.M. Chapman, and O.T. Wong Anti-Cancer Drugs 5 1994 75 82
7. S. Makonkawkeyoon, R.N.R. Limson-Pobre, A.L. Moreira, V. Schauf, and G. Kaplan Proc. Natl. Acad. Sci. U. S. A. 90 1993 5974 5978
8. W.D. Figg, S. Raje, K.S. Bauer, A. Tompkins, D. Venzon, R. Bergan, A. Chen, M. Hamilton, J. Pluda, and E. Reed J. Pharm. Sci. 88 1999 121 125
9. E. Atra, and E.I. Sato Clin. Exp. Rheumatol. 11 1993 487 493
10. S. Ochonisky, J. Verroust, S. Bastuji-Garin, R. Gherardi, and J. Revuz Arch. Dermatol. 130 1994 66 69
11. H. Miyachi, A. Azuma, A. Ogasawara, E. Uchimura, N. Watanabe, Y. Kobayashi, F. Kato, M. Kato, and Y. Hashimoto J. Med. Chem. 40 1997 2858 2865
12. G. Chen, X. Zhang, S. Zhang, T. Chen, and Y. Wu J. Appl. Polym. Sci. 106 2007 2808 2816
13. X. Li, J. Zhan, and Y. Li Macromolecules 37 2004 7584 7594
14. D. Hellwinkel, R. Lenz, and F. Laemmerzahl Tetrahedron 39 1983 2073 2084
15. M. Mori, K. Chiba, N. Ohta, and Y. Ban Heterocycles 13 1979 329 332
16. R.J. Perry, and S.R. Turner J. Org. Chem. 56 1991 6573 6576
17. H. Cao, and H. Alper Org. Lett. 12 2010 4126 4129
18. S.A. Worlikar, and R.C. Larock J. Org. Chem. 73 2008 7175 7180
19. A. Takacs, P. Acs, and L. Kollar Tetrahedron 64 2008 983 987
20. J.R. Martinelli, D.A. Watson, D.M. Freckmann, T.E. Barder, and S.L. Buchwald J. Org. Chem. 73 2008 7102 7107
21. Y. Du, T.K. Hyster, and T. Rovis Chem. Commun. 47 2011 12074 12076
22. A. Begouin, and P. Queiroz Eur. J. Org. Chem. 17 2009 2820 2827
23. M.V. Khedkar, S.R. Khan, K.P. Dhake, and B.M. Bhanage Synthesis 44 2012 2623 2629
24. M.V. Khedkar, T. Sasaki, and B.M. Bhanage RSC Adv. 3 2013 7791 7797
25. T. Sasaki, C. Zhong, M. Tada, and Y. Iwasawa Chem. Commun. 19 2005 2506 2508
26. T. Sasaki, M. Tada, C. Zhong, T. Kume, and Y. Iwasawa J. Mol. Catal. A: Chem. 279 2008 200 209
27. M.V. Khedkar, T. Sasaki, and B.M. Bhanage ACS Catal. 3 2013 287 293
28. M.V. Khedkar, and B.M. Bhanage Front. Chem. Sci. Eng. 7 2013 226 230
29. J. Hsieh, and C. Cheng Chem. Commun. 36 2005 4554 4556
30. H.B. Lempers, and R.A. Sheldon J. Catal. 175 1998 62 69