Electrochemical synthesis of 3,5-disubstituted isoxazoles

Journal of Electroanalytical Chemistry

Volumn 727, Issue , 2014, Pages 120-124

  Xiao, Huan Lan ^a   Zeng, Cheng Chu ^a   Tian, Hong Yu ^b   Hu, Li Ming ^a   Little, R Daniel ^c  

^a BEIJING UNIVERSITY OF TECHNOLOGY   (China)

^b BEIJING TECHNOLOGY AND BUSINESS UNIVERSITY   (China)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Chalcone oximes; Electrochemical synthesis; Isoxazoles

Indexed keywords

CYCLIC VOLTAMMETRY; ELECTROCHEMICAL OXIDATION; REACTION INTERMEDIATES; SYNTHESIS (CHEMICAL);

3 ,5-DISUBSTITUTED ISOXAZOLES; CHALCONES; CYCLIC VOLTAMMOGRAMS; ELECTROCHEMICAL SYNTHESIS; ISOXAZOLES; REACTION MECHANISM; SUPPORTING ELECTROLYTE; WORKING ELECTRODE;

ELECTROLYSIS;

EID: 84903984784     PISSN: 15726657     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jelechem.2014.06.008     Document Type: Article

References (43)

1. X.L. Wang, K. Wan, and C.H. Zhou Eur. J. Med. Chem. 45 2010 4631 4639
2. A. Kumar, S. Rout, C.S. Panda, M.B.V. Raju, and B.V.V. Ravikumar J. Adv. Pharm. Res. 2 2011 94 101
3. E. Rajanarendara, M.N. Reddy, K.R. Murthy, K.G. Reddy, S. Raju, M. Srinivas, B. Praveen, and M.S. Rao Bioorg. Med. Chem. Lett. 20 2010 6052 6055
4. A. Srinivas, A. Nagaraj, and C.S. Reddy Eur. J. Med. Chem. 45 2010 2353 2358
5. A. Kamal, J.S. Reddy, M.J. Ramaiah, D. Dastagiri, E.V. Bharathi, M.A. Azhar, F. Sultana, S. Pushpavalli, M.P. Bhadra, A. Juvekar, S. Sen, and S. Zingde Eur. J. Med. Chem. 45 2010 3924 3937
6. A. Padmaja, T. Payani, G. Dinneswara, and V. Padmavathi Eur. J. Med. Chem. 44 2009 4557 4566
7. H. Takikawa, A. Takada, K. Hikita, and K. Suzuki Angew. Chem. Int. Ed. 47 2008 7446 7449
8. C. Kashima Heterocycles 12 1979 1343 1368
9. P.G. Baraldi, A. Barco, S. Benetti, G.P. Pollini, and D. Simoni Synthesis 1987 857 869
10. A.I. Kotyatkina, V.N. Zhabinsky, and V.A. Khripach Russ. Chem. Rev. 70 2001 641 653
11. V. Jaeger, and P.A. Colinas Synthetic Application of 1,3-Dipolar Cycloaddition Chemistry towards Heterocycles A. Padwa, Natural Products vol. 59 2002 Wiley Hoboken 361
12. T. Mukaiyama, and T. Hoshino J. Am. Chem. Soc. 82 1960 5339 5342
13. S. Dadiboyena, J. Xu, and A.T. Hamme Tetrahedron Lett. 48 2007 1295 1298
14. M. Pinho, and M.V.D. Teresa Curr. Org. Chem. 9 2005 925 958
15. F. Himo, T. Lovell, R. Hilgraf, V.V. Rostovstev, L. Noodleman, K.B. Sharpless, and V.V. Fokin J. Am. Chem. Soc. 127 2004 210 216
16. S. Grecian, and V.V. Fokin Angew. Chem. Int. Ed. 47 2008 8285 8287
17. J.T. Brian, A. Mendelsohn, and M.A. Ciufolini J. Org. Chem. 76 2011 728 731
18. B.A. Mendelsohn, S. Lee, S. Kim, F. Teyssier, V.S. Aulakh, and M.A. Ciufolini Org. Lett. 11 2009 1539 1542
19. A.M. Jawalekar, E. Reubsaet, F.P.J.T. Rutjes, and F.L. van Delft Chem. Commun. 47 2011 3198 3200
20. S. Minakata, S. Okumura, T. Nagamachi, and Y. Takeda Org. Lett. 13 2011 2966 2969
21. A. Yoshimura, C.J. Zhu, K.R. Middleton, A.D. Todora, B.J. Kastern, A.V. Maskaev, and V.V. Zhdankin Chem. Commun. 49 2013 4800 4802
22. A. Yoshimura, K.R. Middleton, A.D. Todora, B.J. Kastern, S.R. Koski, A.V. Maskaev, and V.V. Zhdankin Org. Lett. 15 2013 4010 4013
23. S.B. Tang, J.M. He, Y.Q. Sun, L. He, and X.G. She J. Org. Chem. 75 2010 1961 1966
24. H. Valizadeh, M. Amiri, and H. Gholipur J. Heterocyclic Chem. 46 2009 108 110
25. M.M. Heravi, F. Derikvand, A. Haeri, H.A. Oskooie, and F.F. Bamoharram Synth. Commun. 38 2008 135 140
26. R.F. Kurangi, R. Kawthankar, S. Sawal, V.G. Desai, and S.G. Tilve Synth. Commun. 37 2007 587 589
27. V.G. Desai, and S.G. Tilve Synth. Commun. 29 1999 3017 3020
28. J.I. Yoshida, K. Kataoka, R. Horcajada, and A. Nagaki Chem. Rev. 108 2008 2265 2299
29. R. Francke, and R.D. Little Chem. Soc. Rev. 43 2014 2492 2521
30. H.Y. Ma, Z.G. Zha, Z.L. Zhang, M. Li, and Z.Y. Wang Chin. Chem. Lett. 24 2013 780 782
31. B.H. Kim, Y.M. Jun, Y.R. Choi, D.B. Lee, and W. Baik Heterocycles 48 1998 749 754
32. For EGB-induced reaction, see review: Y.N. Ogibin, M.N. Elinson, and G.I. Nikishin Russ. Chem. Rev. 78 2009 89 140
33. Z.Z. Zhang, N.T. Zhang, L.M. Hu, Z.Q. Wei, C.C. Zeng, R.G. Zhong, and Y.B. She RSC Adv. 1 2011 1383 1388
34. J.E. Grob, J. Nunez, M.A. Dechantsreiter, and L.G. Hamann J. Org. Chem. 76 2011 10241 10248
35. C. Praveen, A. Kalyanasundaram, and P.T. Perumal Synlett 5 2010 777 781
36. J. Kaffy, C. Monneret, P. Mailliet, A. Commercon, and R. Pontikis Tetrahedron Lett. 45 2004 3359 3362
37. S. Tang, J. He, Y. Sun, L. He, and X. She Org. Lett. 11 2009 3982 3985
38. I. Chopra, R.K. Walia, and R. Singh Pesticide Res. J. 18 2006 124 128
39. X. Wei, J. Fang, Y. Hu, and H. Hu Synthesis 12 1992 1205 1206
40. T.D. Fulmer, L.P. Dasher, B.L. Bobb, J.D. Wilson, K.L. Sides, and C.F. Beam J. Heterocyclic Chem. 17 1980 799 800
41. S.M. Zhu, Z.G. Lu, and H.W. Hu Chin. J. Anal. Chem. 23 1995 865 869
42. S.M. Xia, Q.W. Hu, and H.W. Hu Chem. J. Chinese Univ. 14 1993 1692 1696
43. K. Saito, M. Hattori, T. Sato, and K. Takahashi Heterocycles 34 1992 129 133