A new preparative method of aryl sulfonate esters by using cyclic organobismuth reagents

Heterocycles

Volumn 74, Issue C, 2007, Pages 771-790

  Sakurai, Naoto ^a   Mukaiyama, Teruaki ^a  

^a KITASATO INSTITUTE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 40849089220     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-07-s(w)63     Document Type: Article

References (52)

1. For reviews on organobismuth chemistry, see:. Abramovitch R.A., and Barton D.H.R. J.-P. Finet. Tetrahedron 44 (1988) 3039
2. Barton D.H.R., and Finet J.-P. Pure AppL Chem. 59 (1987) 937
3. Finet J.-P. Chem. Rev. 89 (1989) 1487
4. Elliott G.I., and Konopelski J.P. Tetrahedron 57 (2001) 5683
5. Suzuki H., Ogawa T., Komatsu N., Matano Y., Murafuji T., and Ikegami T. Organobismuth Chemistry (2001), Elsevier, Amsterdam
6. Freedman L.D., and Doak G.O. Chem. Rev. 82 (1982) 15
7. Suzuki H., Ikegami T., and Matano Y. Synthesis (1997) 249
8. Ikegai K., and Mukaiyama T. Chem. Lett. 34 (2005) 1496
9. Ikegai K., Nagata Y., and Mukaiyama T. Bull. Chem. Soc. Jpn. 79 (2006) 761
10. Ikegai K., Fukumoto K., and Mukaiyama T. Chem. Lett. 35 (2006) 612
11. Mukaiyama T., Sakurai N., and Ikegai K. Chem. Lett. 35 (2006) 1140
12. Sakurai N., Ikegai K., and Mukaiyama T. Arkivoc 7 (2007) 254
13. Imachi S., and Mukaiyama T. Chem. Lett. 36 (2007) 718
14. Dodonov V.A., Starostina T.I., Kuznetsova Y.L., and Gushchin A.V. Russ. Chem. Bull. 44 (1995) 151
15. Barton D.H.R., Finet J.-P., Giannotti C., and Halley F. J. Chem. Soc., Perkin Trans. 1 (1987) 241
16. Barton D.H.R., Finet J.-P., Motherwell W.B., and Pichon C. J. Chem. Soc., Perkin Trans. 1 (1987) 251
17. Fedorov A., Combes S., and Finet J.-P. Tetrahedron 55 (1999) 1341
18. Combes S., and Finet J.-P. Tetrahedron 55 (1999) 3377
19. Suzuki H., Murafuji T., and Azuma N. J. Chem. Soc., Perkin Trans. 1 (1992) 1593
20. Sakurai N., and Mukaiyama T. Chem. Lett. 36 (2007) 928
21. Greene T.W., and Wuts P.G.M. Protective Groups in Organic Synthesis (1999), Wiley, New York 285-287
22. Ohgiya T., and Nishiyama S. Tetrahedron Lett. 45 (2004) 6317
23. Nayak S.K. Synthesis (2000) 1575
24. Ritter K. Synthesis (1993) 735
25. Hartwig J.F. Angew. Chem. Int. Ed. 37 (1998) 2046
26. Miyaura N. Top. Curr. Chem. 219 (2002) 11
27. For recent examples of Suzuki coupling, see:. Tang Z.-Y., Spinella S., and Hu Q.-S. Tetrahedron Lett. 47 (2006) 2427
28. Tang Z.-Y., and Hu Q.-S. J. Am. Chem. Soc. 126 (2004) 3058
29. For recent examples of Kumada coupling, see:. Ackermann L., and Althammer A. Org. Lett. 8 (2006) 3457
30. Limmert M.E., Roy A.H., and Hartwig J.F. J. Org. Chem. 70 (2005) 9364
31. For a recent example of carbonylation, see:. Cai C., Rivera N.R., Balsells J., Sidler R.R., McWilliams J.C., Shultz C.S., and Sun Y. Org. Lett. 8 (2006) 5161
32. For recent examples of modification method without use of an organic base, see:. Fazaeli R., Tangestaninejad S., and Aliyan H. Can. J. Chem. 84 (2006) 812
33. Xu L., and Xia C. Synth. Commun. 34 (2004) 1199
34. Yoneda N., Fukuhara T., Mizokami T., and Suzuki A. Chem. Lett. (1991) 459
35. Barbero M., Degani I., Dughera S., Fochi R., and Perracino P. Synthesis (1998) 90
36. Ogawa T., Ikegami T., Hikasa T., Ono N., and Suzuki H. J. Chem. Soc., Perkin Trans. 1 (1994) 3479
37. Suzuki H., Ikegami T., and Azuma N. J. Chem. Sot., Perkin Trans. 1 (1997) 1609
38. Arnauld T., Barton D.H.R., and Doris E. Tetrahedron 53 (1997) 4137
39. Fedorov A.Y., and Finet J.-P. J. Chem. Soc., Perkin Trans. 1 (2000) 3775
40. Rottendorfand H., and Stemhell S. Aust. J. Chem. 16 (1963) 647
41. Civitello E.R., and Rapoport H. J. Org. Chem. 57 (1992) 834
42. Kenner G.W., and Murray M.A. J. Chem. Soc. (1949) s178
43. Langler R.F., Paddock R.L., Thompson D.B., Crandall I., Ciach M., and Kain K.C. Aust. J. Chem. 56 (2003) 1127
44. Fry S.E., and Pienta N.J. J. Am. Chem. Soc. 107 (1985) 6399
45. Sharghi H., and Shahsavari-Fard Z. Helv. Chim. Acta 88 (2005) 42
46. Kazemi F., Massah A.R., and Javaherian M. Tetrahedron 63 (2007) 5083
47. Choi J.H., Lee B.C., Lee H.W., and Lee I. J. Org. Chem. 67 (2002) 1277
48. Baarschers W.H. Can. J. Chem. 54 (1976) 3056
49. Truce W.E., and VanGemert B. J. Am. Chem. Soc. 100 (1978) 5525
50. Kariyone K., Yagi H., Yamagishi H., and Tanaka M. JP patent 53073434 (1978)
51. Carnahan Jr. J.C., Closson W.D., Ganson J.R., Juckett D.A., and Quaal K.S. J. Am. Chem. Soc. 98 (1976) 2526
52. Kwong F.Y., Lai C.W., Yu M., Tian Y., and Chan K.S. Tetrahedron 59 (2003) 10295