Microwave-assisted cross-coupling reaction of alkynylstibanes with aryl iodides in the presence of ammonium salt

Chemical and Pharmaceutical Bulletin

Volumn 53, Issue 10, 2005, Pages 1369-1371

  Kakusawa, Naoki ^a   Kurita, Jyoji ^a  

^a HOKURIKU UNIVERSITY   (Japan)

Author keywords

Alkynylstibane; Aryl iodide; Cross coupling; Microwave; Palladium catalyst; Phase transfer catalyst

Indexed keywords

ALKYNE DERIVATIVE; AMMONIA; CETRIMIDE; DIMETHYL SULFOXIDE; IODINE DERIVATIVE;

ARTICLE; CATALYSIS; CATALYST; CROSS COUPLING REACTION; HEATING; MICROWAVE RADIATION;

ANTIMONY; CATALYSIS; CETRIMONIUM COMPOUNDS; HYDROCARBONS, IODINATED; MICROWAVES; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS;

EID: 26444436308     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.53.1369     Document Type: Article

References (33)

1. Hayes B. L., "Microwave Synthesis; Chemistry at the Speed of Light," CEM Publishing, Matthews, NC, 2002.
2. Loupy A., "Microwave in Organic Synthesis," Wiley-VCH, Weinheim, 2002.
3. De la Hoz A., Díaz-Ortiz Á., Moreno A., Chem. Soc. Rev., 34, 164-178 (2005).
4. Leadbeater N. E., Torenius H. M., Tye H., Combinatorial Chemistry & High Throughput Screening, 7, 511-528 (2004).
5. Larhed M., Moberg C., Hallberg A., Acc. Chem. Res., 35, 717-727 (2002).
6. Lidström P., Tierney J., Wathey B., Westman J., Tetrahedron, 57, 9225-9283 (2001).
7. Kakusawa N., Yamaguchi K., Kurita J., Tsuchiya T., Tetrahedron Lett., 41, 4143-4146 (2000).
8. Kakusawa N., Yamaguchi K., Kurita J., J. Organomet. Chem., 690, 2956-2966 (2005).
9. Kakusawa N., Tobiyasu T., Yasuike S., Yamaguchi K., Seki H., Kurita J., Tetrahedron Lett., 44, 8589-8592 (2003).
10. Sørensen U. S., Pombo-Villar E., Tetrahedron, 61, 2697-2703 (2005).
11. Seganish M. W., DeShong P., Org. Lett., 6, 4379-4381 (2004).
12. Wang Y., Sauer D. R., Org. Lett., 6, 2793-2796 (2004).
13. Zhang W., Chen C. H.-T., Lu Y., Nagashima T., Org. Lett., 6, 1473-1476 (2004).
14. Leadbeater N. L., Marco M., Tominack B. J., Org. Lett., 5, 3919-3922 (2003).
15. Stanetty P., Schnürch M., Mihovilovic M. D., Synlett, 2003, 1862-1864 (2003).
16. Maes B. U. W., Loones K. T. J., Lemière G. L. F., Dommisse R. A., Synlett, 2003, 1822-1825 (2003).
17. Khalafi-Nezhad A., Zarea A., Soltani Rad M. N., Mokhtari B., Parhami A., Synthesis, 2005, 419-424 (2005).
18. Botella L., Nájera C., Tetrahedron, 60, 5563-5570 (2004).
19. Leadbeater N. E., Marco M., J. Org. Chem., 68, 5660-5667 (2003).
20. Leadbeater N. E., Marco M., Angew. Chem., Int. Ed., 42, 1407-1409 (2003).
21. Leadbeater N. E., Marco M., Org. Lett., 4, 2973-2976 (2002).
22. Habermann J., Ponzi S., Ley S. V., Mini-Reviews in Organic Chemistry, 2, 125-137 (2005).
23. Liao M., Duan X., Liang Y., Tetrahedron Lett., 46, 3469-3472 (2005).
24. Xie X., Lu J., Chen B., Han J., She X., Pan X., Tetrahedron Lett., 45, 809-811 (2004).
25. Ranu B. C., Jana R., Dey S. S., Chem. Lett., 33, 274-275 (2004).
26. Leadbeater N. E., Torenius H. M., Tye H., Tetrahedron, 59, 2253-2258 (2003).
27. Vallin K. S. A., Emilsson P., Larhed M., Hallberg A., J. Org. Chem., 67, 6243-6246 (2002).
28. Leadbeater N. E., Torenius H. M., J. Org. Chem., 67, 3145-3148 (2002).
29. R=10.67 min).
30. Negishi E., Anastasia L., Chem. Rev., 103, 1979-2017 (2003).
31. Littke A. F., Fu G. C., Angew. Chem. Int. Ed., 41, 4176-4211 (2002).
32. Herrmann W. A., Böhm V. P. W., Reisinger C.-P., J. Organomet. Chem., 576, 23-41 (1999).
33. Yang B. H., Buchwald S. L., J. Organomet. Chem., 576, 125-146 (1999).