Corrigendum to "Photochromism of dihydroindolizines. Part XVI: first attempts toward molecular wires comprising photochromic dihydro 5-azaindolizines and π-extended ethynyl and butadiynyl oxadiazole derivatives" [Tetrahedron Lett. 51 (2010) 730] (DOI:10.1016/j.tetlet.2009.11.117);Photochromism of dihydroindolizines. Part XVI: first attempts toward molecular wires comprising photochromic dihydro 5-azaindolizines and π-extended ethynyl and butadiynyl oxadiazole derivatives

Tetrahedron Letters

Volumn 51, Issue 4, 2010, Pages 730-733

  Ahmed, Saleh Abdel Mgeed ^a,b  

^a Assiut University   (Egypt)

^b TAIBAH UNIVERSITY   (Saudi Arabia)

Author keywords

Dihydro 5 azaindolizines (DHAI); Molecular wires; Oxadiazole (OXD); Photochromism; Sonogashira coupling

Indexed keywords

1,3,4 OXADIAZOLE DERIVATIVE; ACETYLENE DERIVATIVE; BETAINE DERIVATIVE; DIHYDRO 5 AZAINDOLIZINE DERIVATIVE; FLUORENE; INDOLIZINE DERIVATIVE; NANOWIRE; PALLADIUM; UNCLASSIFIED DRUG;

ARTICLE; COLOR; IRRADIATION; LIGHT; PHOTOCHEMISTRY; REACTION ANALYSIS; SONOGASHIRA REACTION; SYNTHESIS;

EID: 72149129463     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.02.047     Document Type: Erratum

References (33)

1. Sonogashira K. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 3 (1991), Pergamon Press, Oxford 521
2. Sonogashira K. In: Diederich F., and Stang P.J. (Eds). Metal Catalyzed Cross-Coupling Reactions (1998), Wiley VCH, Weinheim 203
3. Sonogashira K. J. Organomet. Chem. 653 (2002) 46
4. Bunz U.H.F. Chem. Rev. 100 (2000) 1065
5. Tour J.M. Acc. Chem. Res. 33 (2000) 791
6. Robertson N., and McGowan C.A. Chem. Soc. Rev. 32 (2003) 96
7. Redmore N.P., Rubstov I.V., and Therien M.J. J. Am. Chem. Soc. 125 (2003) 8769
8. Screen T.O., Thorne J.R.G., Denning R.G., Bucknall D.G., and Anderson H.L. J. Mater. Chem. 13 (2003) 2796
9. Dembinski R., Bartik T., Bartik B., Jaegerr M., and Gladysz J.A. J. Am. Chem. Soc. 122 (2000) 810
10. Benniston A.C., Harriman A., Li P., and Sams C.A. J. Am. Chem. Soc. 127 (2005) 2553
11. Mohr W., Stahl J., Hampel F., and Gladysz J.A. Chem. Eur. J. 9 (2003) 3324
12. Wang C., Palsson L.O., Batsanov A.S., and Bryce M.R. J. Am. Chem. Soc. 128 (2006) 3789
13. Wang C., Jung G.Y., Batsanov A.S., Bryce M.R., and Petty M.C. J. Mater. Chem. 12 (2002) 173
14. Chien Y.-Y., Wong K.-T., Chou P.-T., and Cheng Y.-M. Chem. Commun. (2002) 2874
15. Wang C., Batsanov A.S., and Bryce M.R. Chem. Commun. (2004) 578
16. Dürr H. Angew. Chem., Int. Ed. Engl. 28 (1989) 413
17. Gross H., and Dürr H. Angew. Chem., Int. Ed. Engl. 21 (1982) 216
18. The photochromic compounds can be considered as photochromic dihydropyrrolo[1,2-b]pyridazines.
19. Terazono Y., Kodis G., Andreasson J., Jeong G., Brune A., Hartmann Th., Dürr H., Moore A.L., Moore S.A., and Gust G. J. Phys. Chem. B 108 (2004) 1812
20. Kodis G., Liddell P.A., de la Garza L., Clausen P.C., Lindsey J.S., Moore A.L., Moore T.A., and Gust D. J. Phys. Chem. A 106 (2002) 2036
21. Tan Y.S., Ahmed S.A., Dürr H., Huch V., and Abdel-Wahab A.A. Chem. Commun. (2001) 1246
22. Ahmed S.A., Abdel-Wahab A.A., and Dürr H. J. Photochem. Photobiol. 154 (2003) 131
23. Ahmed S.A., and Dürr H. Mol. Cryst. Liq. Cryst. 431 (2005) 275
24. Ahmed S.A., Hartmann Th., and Dürr H. J. Photochem. Photobiol. 200 (2008) 50
25. Ahmed S.A., Abdel-Wahab A.A., and Dürr H. In: Horspool W.M., and Lenci F. (Eds). CRC Handbook of Organic Photochemistry and Photobiology. 2nd ed. (2003), CRC Press, New York
26. Ahmed S.A. Monatsh. Chem. 135 (2004) 1173
27. Ahmed S.A. J. Phys. Org. Chem. 15 (2002) 392
28. Ahmed S.A. J. Phys. Org. Chem. 19 (2006) 402
29. Ahmed S.A. J. Phys. Org. Chem. 20 (2007) 564
30. Ahmed S.A., and Pozzo J.L. J. Photochem. Photobiol. 200 (2008) 57
31. Ahmed S.A. Tetrahedron 65 (2009) 1373
32. Ahmed, S. A. Res. Lett. Org. Chem. 2008, Article ID 959372, p 5.
33. Ahmed, S. A. J. Phys. Org. Chem., accepted for publication.