Microwave-assisted and light-induced catalytic ring opening of α-epoxyketones using DDQ

Journal of Molecular Catalysis A: Chemical

Volumn 274, Issue 1-2, 2007, Pages 224-230

  Memarian, H R ^a   Saffar Teluri, A ^a  

^a UNIVERSITY OF ISFAHAN   (Iran)

Author keywords

Epoxyketones; Conductometric; Cyclic voltammetric; Microwave; Ring opening

Indexed keywords

CATALYST ACTIVITY; CYCLIC VOLTAMMETRY; MICROWAVE IRRADIATION; REACTION RATES; ULTRAVIOLET RADIATION;

CONDUCTOMETRICS; EPOXYKETONES; RING OPENING;

KETONES;

EID: 34547422300     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2007.05.010     Document Type: Article

References (61)

1. Farand J.A., Denissova I., and Barriault L. Heterocycles 62 (2004) 735-748
2. Li X., Kyne R.E., and Ovaska T.V. Org. Lett. 8 (2006) 5153-5156
3. Blomberg D., Brickmann K., and Kihlberg J. Tetrahedron 62 (2006) 10937-10944
4. Hajipour A.R., Rafiee F., and Ruoho A.E. Synth. Commun. 36 (2006) 2563-2568
5. Evangelista E.A., Couri M.R.C., Raslan D.S., and Alves R.B. Heteroatom Chem. 17 (2006) 239-244
6. Sridhar G., Gunasundari T., and Roghunathan R. Tetrahedron Lett. 48 (2007) 319-322
7. Hartung J., Daniel K., Gottwald T., Gvob A., and Schneiders N. Org. Biol. Chem. 4 (2006) 2313-2322
8. Zhou J.-F., Song Y.-Z., Zhu F.-X., and Zhu Y.-L. Synth. Commun. 36 (2006) 3297-3303
9. Gupta S., Macala M., and Schafmeister C.E. J. Org. Chem. 71 (2006) 8691-8695
10. Ashry E.S.H.E., Kassem A.A., and Ramadan E. Adv. Heterocycl. Chem. 90 (2006) 1-123
11. Silva V.L.M., Silva A.M.S., Pinto D.C.G.A., and Cavalerio J.A.S. Synlett (2006) 1369-1373
12. Joshi B.P., Sharma A., and Sinha A.K. Tetrahedron 62 (2006) 2590-2593
13. Yadav P.P., Ahmad G., and Maurya R. Tetrahedron Lett. 46 (2005) 5621-5624
14. Manley J.M., Roper T.J., and Lash T.D. J. Org. Chem. 70 (2005) 874-891
15. Somogyi L. Heterocycles 63 (2004) 2243-2267
16. Hilt G., Galbiat F., and Harms K. Synthesis 21 (2006) 3575-3584
17. Habonimana P., Claessens S., and De Kimpe N. Synlett 15 (2006) 2472-2475
18. Shimizu M., Takahashi A., and Kawai S. Org. Lett. 8 (2006) 3585-3587
19. Es-Safi N.-E., and Ducrot P.-H. Lett. Org. Chem. 3 (2006) 231-234
20. Ka Y.L., Gowrisankar S., and Jae N.K. Tetrahedron Lett. 46 (2005) 5387-5391
21. Yan J., Jin S., and Wang B. Tetrahedron Lett. 46 (2005) 8503-8505
22. Nemoto N., Imai K., Umemiya J., and Kouno S. Polym. Preprints Jpn. 54 (2005) 340
23. Diaper C.M., Goldring W.P.D., and Pattenden G. Org. Biol. Chem. 1 (2003) 3949-3959
24. Duymus H., Arslan M., Kucukislamoglu M., and Zengin M. Spectrochim. Acta A 65 (2006) 1120-1124
25. Pundeeswaran M., and Elango K.P. Spectrochim. Acta A 65 (2006) 1148-1153
26. Refat M.S., and El-Didamong A.M. Spectrochim. Acta A 65 (2006) 732-741
27. El-Mossalamy E.H. J. Mol. Liq. 123 (2006) 118-123
28. Guber M., and Al-Shihry S.S. Spectrochim. Acta A 62 (2005) 526-531
29. Yakuplianoglu F., Arslan M., and Yildiz S.Z. Opt. Mater. 27 (2005) 1153-1158
30. Mathew L., and Sankararaman S. J. Org. Chem. 58 (1993) 7576-7577
31. Abdur Rahim M., Matsumura S., and Toshima K. Tetrahedron Lett. 46 (2005) 7307-7309
32. Lu Y.-F., and Fallis A.G. Can. J. Chem. 73 (1995) 2239-2252
33. Santa Deepthi K., Sahadeva Reddy D., Reddy P.P., and Reddy P.S.N. Indian J. Chem. B 39 (2000) 220-222
34. Joshi B.P., Sharma A., and Sinha A.K. Can. J. Chem. 83 (2005) 1826-1832
35. Minetto G., Lampariello L.R., and Taddei M. Synlett (2005) 2743-2746
36. Memarian H.R., Hesami A., Nikpour F., and Döpp D. Indian J. Chem. B 40 (2001) 662-666
37. Memarian H.R., and Nikpour F. Molecules 6 (2001) 63-71
38. Memarian H.R., and Nikpour F. Monatsh. Chem. 133 (2002) 1045-1053
39. Memarian H.R., and Nikpour F. J. Chin. Chem. Soc. 49 (2002) 401-406
40. Memarian H.R., Saffar-Teluri A., and Amini M.K. Heterocycles 68 (2006) 1861-1874
41. Hasegawa E., Ishiyama K., Fujita T., Kato T., and Abe T. J. Org. Chem. 62 (1997) 2396-2400
42. Hasegawa E., Yoneoka A., Suzuki K., Kato T., Kitazume T., and Yanagi K. Tetrahedron 55 (1999) 12957-12968
43. Hasegawa E., Kato T., Kitazume T., Yanagi K., Hasegawa K., and Horaguchi T. Tetrahedron Lett. 37 (1996) 7079-7082
44. Hasegawa E., Ishiyama K., Kato K., Horaguchi T., Shimizu T., Tanaka S., and Yamashita Y. J. Org. Chem. 57 (1992) 5352-5359
45. Hasegawa E., and Kamata M. In: Horspool W.M., and Lenci F. (Eds). CRC Handbook of Organic Photochemistry and Photobiology (2004), CRC Press, Boca Raton 1-17 Chapter 53
46. Okada K., Hasegawa E., and Mukai T. Chem. Lett. (1983) 305-308
47. Hasegawa E., Ishiyama K., Kashiwazaki H., Horaguchi T., and Shimizu T. Tetrahedron Lett. 31 (1990) 4045-4048
48. Hardouin C., Chevallier F., Rousseau B., and Doris E. J. Org. Chem. 66 (2001) 1046-1048
49. Lopez L., and Troisi L. Tetrahedron Lett. 30 (1989) 3097-3100
50. Kagan J., Juang P.Y., Firth B.E., Przybytek J.T., and Singh S.P. Tetrahedron Lett. (1977) 4289-4290
51. Huo C., Jia X., Zhang W., Yang L., Lu J., and Liu Z.-L. Synlett (2004) 251-254
52. Delaunay J., Lebouc A., Tallaec A., and Sinonet J. J. Chem. Soc. Chem. Commun. (1982) 387-388
53. Kampars V., and Neiland O. Russ. Chem. Rev. 46 (1977) 503-513
54. Cram D.J., and Abd Elhafez F.A. J. Am. Chem. Soc. 74 (1952) 5828-5835
55. Hubig S.M., Bockman T.M., and Kochi J.K. J. Am. Chem. Soc. 119 (1997) 2926-2935
56. Rehm D., and Weller A. Isr. J. Chem. 8 (1970) 259
57. Dwivedi P.C., Banga P.K., and Agarwal R. Electrochim. Acta 27 (1982) 1697-1699
58. Bougrin K., Loupy A., and Soufiaoui M. J. Photochem. Photobiolog. C: Photochem. Rev. 6 (2005) 139-167
59. Loupy A., and Perreux L. Tetrahedron 57 (2001) 9199-9253
60. Kumar C.V., Ramaiah D., Das P.K., and George M.W. J. Org. Chem. 50 (1985) 2818-2824
61. Rohrmann R., Jones G., and Shonle A. J. Am. Chem. Soc. 66 (1944) 1856-1857