Stereospecific synthesis of conjugated (1E,3E)- and (1Z,3Z)-1,4-di(n-N,N- dimethylaminophenyl)-1,3-butadienes from 2-chloro-1-(n-N,N-dimethylaminophenyl) ethenes: Fluorescence properties

Tetrahedron

Volumn 62, Issue 13, 2006, Pages 3075-3080

  Rodriguez, J Gonzalo ^a   Tejedor, J Luis ^a   Rumbero, Angel ^a   Canoira, Laureano ^b  

^a UNIVERSIDAD AUTÓNOMA DE MADRID   (Spain)

^b UNIVERSIDAD POLITÉCNICA DE MADRID   (Spain)

Author keywords

1,4 Diaryl 1,3 butadienes; Homocoupling reaction; Nickel complexes; Stereospecific hydrogenation

Indexed keywords

1,3 BUTADIENE; 1,3 BUTADIENE DERIVATIVE; 1,4 DI(2 N,N DIMETHYLAMINOPHENYL) 1,3 BUTADIENE; 1,4 DI(3 N,N DIMETHYLAMINOPHENYL) 1,3 BUTADIENE; 1,4 DI(4 N,N DIMETHYLAMINOPHENYL) 1,3 BUTADIENE; 1,4 DI(4 N,N DIMETHYLAMINOPHENYL)1,3 BUTADIENE; 1,4 DI(N,N DIMETHYLAMINOPHENYL) 1,3 BUTADIENE; 2 CHLORO 1 (2 N,N DIMETHYLAMINOPHENYL)ETHENE; 2 CHLORO 1 (3 N,N DIMETHYLAMINOPHENYL)ETHENE; 2 CHLORO 1 (4 N,N DIMETHYLAMINOPHENYL)ETHENE; 2 CHLORO 1(N,N DIMETHYLAMINOPHENYL)ETHENE; ALCOHOL; CHLOROVINYL; ETHYLENE DERIVATIVE; NICKEL COMPLEX; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; COLUMN CHROMATOGRAPHY; CONJUGATION; FLUORESCENCE; HYDROGENATION; PRIORITY JOURNAL; RADIATION; REACTION ANALYSIS; STEREOISOMERISM; STEREOSPECIFICITY; STOICHIOMETRY; SUN EXPOSURE; SYNTHESIS; WITTIG REACTION;

EID: 33644756502     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.01.030     Document Type: Article

References (24)

1. I.V. Krivoshel, and M. Skoroboatov Polyacetylene and Polyarylenes: Synthesis and Conducting Properties 1991 Gordon and Breach Science New York
2. G. Pattenden J.F. Stoddart Comprehensive Organic Chemistry Vol. 1 1979 Pergamon Oxford, UK 171 177
3. M.F. Semmelhack, P.M. Helquist, and J.D. Gorzynski J. Am. Chem. Soc. 94 1972 9234
4. M.F. Semmelhack, P.M. Helquist, L.D. Jones, L. Keller, L. Mendelson, L. Speltz, J. Gorzynski Smith, and R.D. Stauffer J. Am. Chem. Soc. 103 1981 6460
5. T.-S. Lee, J. Kim, and J.-Y. Bae Polymer 45 2004 5065
6. R. Baker Chem. Rev. 73 1973 487
7. S. Takahashi, Y. Suzuki, and N. Hagihara Chem. Lett. 1974 1363
8. L.E. Elsom, J.D. Hunt, and A. McKillop Organomet. Chem. Rev. A 8 1972 135
9. R.J.P. Corriu, and J.P. Masse J. Chem. Soc., Chem. Commun. 1972 144
10. K. Tamao, K. Sumitani, and M. Kumada J. Am. Chem. Soc. 94 1972 4374
11. V. Percec, M. Zhao, J.-Y. Bae, A.D. Asandei, and D.H. Hill Polym. Bull. 38 1977 515
12. C. Cannes, S. Condon, M. Durandetti, J. Périchon, and J.-Y. Nédélec J. Org. Chem. 65 2000 4575
13. K.W.R. de Franca, M. Navarro, E. Leonel, M. Durandetti, and J.-Y. Nédélec J. Org. Chem. 67 2002 1838
14. M. Kotora, H. Matsumura, and T. Takahashi Chem. Lett. 3 2000 236 237
15. K. Takagi, N. Hayama, and K. Sasaki Bull. Chem. Soc. Jpn. 57 1984 1887
16. J.G. Rodriguez, S. Ramos, R. Martín-Villamil, I. Fonseca, and A. Albert J. Chem. Soc., Perkin Trans. 1 1996 541
17. J.G. Rodriguez, R. Martín, F.H. Cano, and I. Fonseca J. Chem. Soc., Perkin Trans. 1 1997 709
18. A.J. Hall, and M. Gisler J. Chem. Soc. A 4 1970 571
19. M. Iyoda, M. Sakaitani, H. Otsuka, and M. Oda Chem. Lett. 130 1985 127
20. J.G. Rodríguez, and S. Pleite J. Organomet. Chem. 637-639 2001 230
21. J.G. Rodríguez, A. Lafuente, R. Martín-Villamil, and M.P. Martínez-Alcazar J. Phys. Org. Chem. 14 2001 859
22. J.K. Stille, and B.L. Groh J. Am. Chem. Soc. 109 1987 813
23. J.G. Rodríguez, and L. Canoira J. Heterocycl. Chem. 22 1985 883
24. Y. Benito, L. Canoira, and J.G. Rodríguez Appl. Organomet. Chem. 1 1987 535