A mild and highly efficient one-pot three-component reaction for carbon-sulfur bond formation catalyzed by potassium tert-butoxide

Chinese Chemical Letters

Volumn 22, Issue 10, 2011, Pages 1179-1182

  Movassagh, Barahman ^a   Rakhshani, Amir ^a  

^a K N TOOSI UNIVERSITY OF TECHNOLOGY   (Iran)

Author keywords

C S bond formation; Potassium tert butoxide; Thia Michael adduct; Thiols; Three component reaction

Indexed keywords

EID: 84860414111     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2011.05.015     Document Type: Article

References (44)

1. A. Doemling, and I. Ugi Angew. Chem. Int. Engl. 39 2000 3168
2. U. Schmidt, and E. Ohler Angew. Chem. Int. Ed. Engl. 15 1976 42
3. B.M. Trost, and D.E. Keeley J. Org. Chem. 40 1975 2013
4. M. Shibasaki, A. Nishida, and S.S.J. Ikegami Chem. Soc., Chem. Commun. 1982 1324
5. O. Miyata, T. Shinada, and I. Ninomiya J. Org. Chem. 56 1991 6556
6. O. Miyata, S. Yamaguchi, and I. Ninomiya Chem. Pharm. Bull. 44 1996 636
7. Y. Kita, N. Shibata, and T. Miki Chem. Pharm. Bull. 40 1992 12
8. J.H. Clark Chem. Rev. 80 1980 429
9. K. Nishimura, M. Ono, and Y. Nagaoka J. Am. Chem. Soc. 119 1997 12974
10. T. Cohen, A.J. Mura, and D.W. Shull J. Org. Chem. 41 1976 3218
11. P. Perlmutter Conjugated Addition Reactions in Organic Synthesis 1992 Pergamon Oxford
12. L. Novak, P. Kolonits, and C. Szantay Tetrahedron 38 1982 153
13. H. Hiemstra, and H. Wynberg J. Am. Chem. Soc. 103 1981 417
14. I. Kuwajima, T. Murofushi, and E. Nakamura Synthesis 1976 602
15. M. Zahouily, Y. Abrouki, and A. Rayadh Tetrahedron Lett. 43 2002 7729
16. H. Liu, and T. Cohen J. Org. Chem. 60 1995 2022
17. T.C. Wabnitz, J.Q. Yu, and J.B. Spencer Synlett 2003 1070
18. S. Cheng, and D.D. Comer Tetrahedron Lett. 43 2002 1179
19. G. Sharma, R. Kumar, and A.K. Chakraborti J. Mol. Catal. A: Chem. 263 2007 143
20. G. Sharma, R. Kumar, and A.K. Chakraborti Tetrahedron Lett. 49 2008 4272
21. S. Kobayashi, C. Ogawa, and M. Kawamura Synlett 2001 983
22. B.C. Ranu, S.S. Dey, and S. Samanta Arkivok 2005 44
23. M. Saito, M. Nakajima, and S. Hashimoto Tetrahedron 56 2000 9589
24. B.J. Li, L. Jiang, and M. Liu Synlett 2005 603
25. S.K. Garg, R. Kumar, and A.K. Chakraborti Tetrahedron Lett. 46 2005 1721
26. N. Srivastava, and B.K. Banik J. Org. Chem. 68 2003 2109
27. M. Bandini, P.G. Cozzi, and M. Giacomini J. Org. Chem. 67 2002 3700
28. H. Firouzabadi, N. Iranpoor, and N.A.A. Jafari Adv. Synth. Catal. 347 2005 655
29. M.K. Chaudhuri, and S. Hussain J. Mol. Catal. A: Chem. 269 2007 214
30. G.L. Khatik, R. Kumar, and A.K. Chakraborti Org. Lett. 8 2006 2433
31. Y.O. Sharma, and M.S. Degani J. Mol. Catal. A: Chem. 277 2007 215
32. M. Meciarova, S. Toma, and P. Kotrusz Org. Biomol. Chem. 4 2006 1420
33. B.C. Ranu, and S.S. Dey Tetrahedron 60 2004 4183
34. B.C. Ranu, S.S. Dey, and A. Hajra Tetrahedron 59 2003 2417
35. B. Movassagh, and P. Shayegan Arkivoc 2006 130
36. D.M. Pore, M.S. Soudagar, and U.V. Desai Tetrahedron Lett. 47 2006 9325
37. C.M. Chu, S. Gao, and M.N.V. Sastry Tetrahedron Lett. 46 2005 4971
38. S. Gao, T. Tzeng, and M.N.V. Sastry Tetrahedron Lett. 47 2006 1889
39. C.M. Chu, S. Gao, and M.N.V. Sastry Tetrahedron 63 2007 1863
40. A. Kamal, D.R. Reddy, and Rajendar Tetrahedron Lett. 46 2005 7951
41. H. Firouzabadi, N. Iranpoor, and M. Abbasi Tetrahedron 65 2009 5293
42. H. Zhang, Y. Zhang, and L. Liu Synthesis 2005 2129
43. A. Kumar, and Akanksha Tetrahedron Lett. 48 2007 8730
44. G.L. Khatik, G. Sharma, and R. Kumar Tetrahedron 63 2007 1200