Vinyl selenones: Annulation agents for the synthesis of six-membered benzo-1,4-heterocyclic compounds

Tetrahedron

Volumn 69, Issue 2, 2013, Pages 481-486

  Bagnoli, Luana ^a   Casini, Sara ^a   Marini, Francesca ^a   Santi, Claudio ^a   Testaferri, Lorenzo ^a  

^a UNIVERSITY OF PERUGIA   (Italy)

Author keywords

1,4 Benzodioxines; 1,4 Benzothiines; 1,4 Benzoxazines; MIRC reaction; Vinyl selenones

Indexed keywords

CHEMICAL COMPOUND; HETEROCYCLIC COMPOUND; PHENOL DERIVATIVE; QUINOXALINE DERIVATIVE; UNCLASSIFIED DRUG; VINYL SELENONE;

ADDITION REACTION; ANNULATION REACTION; ARTICLE; CYCLIZATION; PRIORITY JOURNAL; SYNTHESIS;

EID: 84871401792     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.11.036     Document Type: Article

References (40)

1. G. Guillaumet 1,4-Dioxans, Oxathians, Dithians and Benzoderivatives A.J. Boulton, A.R. Katritzky, C.W. Rees, E.F.V. Scriven, Comprehensive Heterocyclic Chemistry II Vol. 6 1996 Pergamon Oxford
2. B. Achari, S.B. Mandal, P.K. Dutta, and C. Chowdhury Synlett 2004 2449 2467
3. G.L. Morgans, E.L. Ngidi, L.G. Madeley, S.D. Khanye, J.P. Michael, C.B. de Koning, and W.A.L. van Otterlo Tetrahedron 65 2009 10650 10659
4. W. Bao, Y. Liu, X. Lv, and W. Qian Org. Lett. 10 2008 3899 3902 and references cited therein
5. A.B. Naidu, D. Ganapathy, and G. Sekar Synthesis 2010 3509 3519
6. A. Arnoldi, A. Bassoli, L. Merlini, and E. Ragg J. Chem. Soc., Perkin Trans. 2 1991 1399 1406
7. Y.R. Zhang, J.W. Xie, X.J. Huang, and W.D. Zhu Org. Biomol. Chem. 10 2012 6554 6561
8. J. Ilas, S.P. Anderluh, M.S. Dolenc, and D. Kikelj Tetrahedron 61 2005 7325 7348 and references cited therein
9. H. Cho, Y. Iwama, K. Sugimoto, S. Mori, and H. Tokuyama J. Org. Chem. 75 2010 627 636
10. H. Matsuoka, N. Ohi, M. Mihara, H. Suzuki, K. Miyamoto, N. Maruyama, K. Tsuji, N. Kato, T. Akimoto, Y. Taketa, K. Yano, and T. Kuroki J. Med. Chem. 40 1997 105 111
11. S.I. Kuwabe, K.E. Torraca, and S.L. Buchwald J. Am. Chem. Soc. 123 2001 12202 12206
12. K.E. Torraca, S.I. Kuwabe, and S.L. Buchwald J. Am. Chem. Soc. 122 2000 12907 12908
13. S. Clavier, M. Khouili, P. Bouyssou, and G. Coudert Tetrahedron 58 2002 1533 1540
14. J.J.V. Eynde, and I. Mailleux Synth. Commun. 31 2001 1 7
15. Y. Harrak, G. Guillaumet, and M.D. Pujol Synlett 2003 813 816
16. D.J. Harrison, and U. Fekl Chem. Commun. 2009 7572 7574
17. W.E. Parham, T.M. Roder, and W.R. Hasek J. Am. Chem. Soc. 75 1953 1647 1651
18. A.B. Pierini, M.T. Baumgartner, and R.A. Rossi J. Org. Chem. 52 1987 1089 1092
19. R. Omar-Amrani, A. Thomas, E. Brenner, R. Schneider, and Y. Fort Org. Lett. 5 2003 2311 2314
20. P. Mizar, and B. Myrboh Tetrahedron Lett. 47 2006 7823 7826
21. D. Albanese, A. Donghi, D. Landini, V. Lupi, and M. Penso Green Chem. 5 2003 367 369
22. C. Buon, L. Chacun-Lefevre, R. Rabot, P. Bouyssou, and G. Coudert Tetrahedron 56 2000 605 614
23. M. Yar, E.M. McGarrigle, and V.K. Aggarwal Org. Lett. 11 2009 257 260
24. M. Yar, E.M. McGarrigle, and V.K. Aggarwal Angew. Chem., Int. Ed. 47 2008 3784 3786
25. Z. Du, C. Zhou, Y. Gao, Q. Ren, K. Zhang, H. Cheng, W. Wang, and J. Wang Org. Biomol. Chem. 10 2012 36 39
26. J. Wang, H. Xie, H. Li, L. Zu, and W. Wang Angew. Chem., Int. Ed. 47 2008 4177 4179
27. L. Bagnoli, C. Scarponi, L. Testaferri, and M. Tiecco Tetrahedron: Asymmetry 20 2009 1506 1514
28. S. Sternativo, F. Marini, F. Del Verme, A. Calandriello, L. Testaferri, and M. Tiecco Tetrahedron 66 2010 6851 6857
29. L. Bagnoli, C. Scarponi, M.G. Rossi, L. Testaferri, and M. Tiecco Chem. - Eur. J. 17 2011 993 999
30. M. Tiecco, D. Chianelli, M. Tingoli, L. Testaferri, and D. Bartoli Tetrahedron 42 1986 4897 4906
31. M. Li, and R. Hua J. Org. Chem. 73 2008 8658 8660 and references cited therein
32. G. Feng, J. Wu, and W.M. Dai Tetrahedron 62 2006 4635 4642
33. G. Bettoni, C. Franchini, R. Perrone, and V. Tortorella Tetrahedron 36 1980 409 415
34. M.K. Ghorai, A.K. Sahoo, and S. Kumar Org. Lett. 13 2011 5972 5975
35. T.C. Eary, and D. Clausen Tetrahedron Lett. 47 2006 6899 6902
36. R.A. Bunce, D.M. Herron, and M.L. Ackerman J. Org. Chem. 65 2000 2847 2850
37. N. Proust, J.C. Gallucci, and L.A. Paquette J. Org. Chem. 74 2009 2897 2900
38. I. Takashi, K. Nagata, M. Miyazaki, H. Ishikawa, A. Kurihara, and A. Ohsawa Tetrahedron 60 2004 6649 6655
39. Y. Masuoka, T. Asako, G. Goto, and S. Noguchi Chem. Pharm. Bull. 34 1986 130 139
40. H. Stetter Chem. Ber. 86 1953 197 205