Corrigendum to "Synthesis of fused imidazo-pyridine and -azepine derivatives by sequential van Leusen/Heck reactions". [Tetrahedron Lett. 47 (2006) 3225] (DOI:10.1016/j.tetlet.2006.03.056);Synthesis of fused imidazo-pyridine and -azepine derivatives by sequential van Leusen/Heck reactions

Tetrahedron Letters

Volumn 47, Issue 19, 2006, Pages 3225-3228

  Beebe, Xenia ^a   Gracias, Vijaya ^a   Djuric, Stevan W ^a  

^a ABBOTT LABORATORIES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AZEPINE DERIVATIVE; CARBON; HETEROCYCLIC COMPOUND; IMIDAZOPYRIDINE DERIVATIVE;

ARTICLE; CHEMICAL BOND; CHEMICAL COMPOSITION; COMPLEX FORMATION; HECK REACTION; MATERIALS; SYNTHESIS;

EID: 33645796228     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.07.115     Document Type: Erratum

References (31)

1. For recent reviews see:. Hulme C., and Gore V. Curr. Med. Chem. 10 (2003) 51-80
2. Hulme C., and Nixey T. Curr. Opin. Drug Discovery Today 6 (2003) 921-929
3. For a recent synthesis of imidazo[1,2-a]pyridines see:. Schwerkoske J., Masquelin T., Perun T., and Hulme C. Tetrahedron Lett. 48 (2005) 8355-8357
4. Marcaccini S., and Torroba T. In: Zhu J., and Bienayme H. (Eds). Multicomponent Reactions (2005), Wiley-VCH, Weinheim Chapter 2
5. Gracias V., Moore J.D., and Djuric S.W. Tetrahedron Lett. 45 (2004) 417-420
6. Akritopoulou-Zanze I., Gracias V., Moore J.D., and Djuric S.W. Tetrahedron Lett. 45 (2004) 3421-3423
7. Akritopoulou-Zanze I., Gracias V., and Djuric S. Tetrahedron Lett. 45 (2004) 8439-8441
8. Vasudevan A., and Verzal M.K. Tetrahedron Lett. 46 (2005) 1697-1701
9. Link J.T. Organic Reactions Vol. 60 (2002), Wiley, Hoboken, NJ Chapter 2
10. Dounay A.B., and Overman L.E. Chem. Rev. 103 (2003) 2945-2963
11. Dounay A.B., Overman L.E., and Wrobleski A.D. J. Am. Chem. Soc. 127 (2005) 10186-10187
12. von Wangelin A.J., Neumann H., Gordes D., Hubner S., Wendler C., Klaus S., Strubing D., Spannenberg A., Jiao H., El Firdoussi L., Thurow K., Stoll N., and Beller M. Synthesis 12 (2005) 2029-2038
13. Barluenga J., Fernandez M.A., Aznar F., and Valdes C. Chem. Eur. J. 11 (2005) 2276-2283
14. Xiang Z., Luo T., Lu K., Cui J., Shi X., Fathi R., Chen J., and Yang Z. Org. Lett. 6 (2004) 3155-3158
15. van Leusen A.M., Wilderman J., and Oldenzeil O.H. J. Org. Chem. 42 (1977) 1153-1159
16. van Leusen A.M. Lect. Heterocycl. Chem. 5 (1980) S-111
17. van Nispen S.P.J.M., Mensink C., and van Leusen A.M. Tetrahedron Lett. 21 (1980) 3723-3726
18. Sisko J., Kassick A.J., Mellinger M., Filan J.J., Allen A., and Olsen M.A. J. Org. Chem. 65 (2000) 1516-1524
19. Almansa C., Alton J., de Arriba A.F., Cavalcanti F.L., Escamilla I., Gomez L.A., Miralles A., Soliva R., Bartroli J., Carceller E., Merlos M., and Garcia-Rafanell J. J. Med. Chem. 46 (2003) 3463-3475
20. Gracias V., Gasiecki A.F., and Djuric S.W. Org. Lett. 7 (2005) 3183-3186
21. Gracias V., Gasiecki A.F., and Djuric S.W. Tetrahedron Lett. 46 (2005) 9049-9052
22. Gracias V., Darczak D., Gasiecki A.F., and Djuric S.W. Tetrahedron Lett. 46 (2005) 9053-9056
23. Bluhm M.E., Ciesielski M., Gorls H., and Doring M. Angew. Chem., Int. Ed. 41 (2002) 2962-2965
24. Langry K.C. J. Org. Chem. 56 (1991) 2400-2404
25. Murashima T., Nishi K., Nakamoto K., Kato A., Tamai R., Uno H., and Ono N. Heterocycles 58 (2002) 301-310
26. Kalinin A.V., Chauder B.A., Rakhit S., and Snieckus V. Org. Lett. 5 (2003) 3519-3521
27. Lee K.L., Goh J.B., and Martin S.F. Tetrahedron Lett. 42 (2001) 1635-1638
28. Harayama T., Sato T., Hori A., Abe H., and Takeuchi Y. Synlett (2003) 1141-1145
29. Jacobson M.A., and Williard P.G. J. Org. Chem. 67 (2002) 3915-3918
30. 3) δ ppm 16.4, 118.9, 120.2, 122.6, 122.8, 124.0, 125.2, 126.9, 127.6, 127.7, 128.3, 128.5, 128.7, 128.8, 129.5, 134.5, 135.8; MS (ESI M+H) 259.
31. Herrmann W.A., Brossmer C., Ofele K., Reisinger C., Priermeier M.B., Beller M., and Fischer H. Angew. Chem., Int. Ed. Engl. 34 (1995) 1844-1848