The synthesis of heteroarylazulene

Heterocycles

Volumn 66, Issue 1, 2005, Pages 91-94

  Shoji, Taku ^a   Kikuchi, Shigeru ^b   Ito, Shunji ^c   Morita, Noboru ^a  

^a TOHOKU UNIVERSITY   (Japan)

^b KUMAMOTO UNIVERSITY   (Japan)

^c HIROSAKI UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33646868079     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-05-S(K)35     Document Type: Article

References (11)

1. Katritzky A.R., and Ress C.W. In: Boulton A.J., and McKillop A. (Eds). In Comprehensive Heterocyclic Chemistry Vol. 2 (1984), Pergamon Press, Inc., New York
2. Martin R.E., and Diederich F. Angew. Chem. Int. Ed. 38 (1999) 1350
3. Balzani V., Credi A., Raymo F.M., and Stoddart J.F. Angew. Chem. Int. Ed. 39 (2000) 3348
4. We have already reported another several types of palladium-catalyzed coupling reactions which concern azulenes. Yokoyama R., Ito S., Okujima T., Kubo T., Yasunami M., Tajiri A., and Morita N. Trtrahedron 59 (2003) 8191
5. Ito S., Inabe H., Morita N., and Tajiri A. Eur. J. Org. Chem. (2004) 1774
6. Ito S., Terazono T., Kubo T., Okujima T., Morita N., Murafuji T., Sugihara Y., Fujimori K., Kawakami J., and Tajiri A. Tetrahedron 60 (2004) 5357
7. Ito S., Kubo T., Morita N., Ikoma T., Tero-Kubota S., Kawakami J., and Tajiri A. J. Org. Chem. 70 (2005) 2285
8. Ito S., Ando M., Nomura A., Morita N., Kabuto C., Mukai H., Ohta K., Kawakami J., Yoshizawa A., and Tajiri A. J. Org. Chem. 70 (2005) 3939
9. Dumouchel S., Mongin F., Trécourt F., and Quéguiner G. Tetrahedron 59 (2003) 8629
10. Ito S., Kubo T., Morita N., Matui Y., Watanabe T., Ohta A., Fujimori K., Murafuji T., Sugihara Y., and Tajiri A. Tetrahedron Lett. 45 (2004) 2891
11. It can be also prepared directly from thiophene itself using lithium magnesate. Bayh O., Awad H., Mongin F., Hoarau C., Trécourt F., Quéguiner F., Blanco F., Abarca B., and Ballesteros R. Tetrahedron 61 (2005) 4779