Intramolecular photocycloaddition of anthracene and benzene ring systems

Tetrahedron Letters

Volumn 43, Issue 38, 2002, Pages 6853-6855

  Cao, Derong ^a   Dobis, Silvia ^b   Meier, Herbert ^b  

^a GUANGZHOU INSTITUTE OF CHEMISTRY   (China)

^b JOHANNES GUTENBERG UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANTHRACENE; BENZENE; METHYL GROUP;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CATALYST; DILUTION; MOLECULAR INTERACTION; PROTON NUCLEAR MAGNETIC RESONANCE; THERMAL ANALYSIS;

STAPHYLOCOCCUS PHAGE 3A;

EID: 0037119792     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01476-4     Document Type: Article

References (17)

1. Meier H., Müller K., Fetten M. J. Inform. Recording. 22:1996;421-426.
2. Newkome G.R., Moorefield C.N., Vögtle F. Dendrimers and Dendrons. 2001;Wiley-VCH, Weinheim.
3. Fréchet J.M.J., Tomalia D.A. Dendrimers and other Dendritic Polymers. 2001;Wiley, New York.
4. Cao, D.; Meier, H. Angew. Chem. 2001, 113, 193-195;
5. Angew. Chem., Int. Ed. 2001, 40, 186-188.
6. q, benzene).
7. 2), 6.57 (t, 1H, p-H, benzene), 6.65 (d, 2H, o-H, benzene), 7.38 (m, 10H, benzene), 7.48, m, 4H/8.01, m, 2H/8.33, m, 2H/8.46, s, 1H (anthracene).
8. 2), 6.54, t, 3H/6.61, d, 2H/6.65, d, 4H/7.36, m, 20H (benzene), 7.38, m, 4H/7.99, m, 2H/8.30, m, 2H/8.44, s, 1H (anthracene).
9. 3), 56.9, 65.7 (C-1, C-5), 71.2 (C-2), 81.1 (C-4), 105.8 (C-6, C-23), 122.8, 125.2, 125.8, 127.7 (C-11, 12, 13, 14, 17, 18, 19, 20), 145.0, 146.8 (C-10, 15, 16, 21), 163.7 (C-7, 22).
10. 4J=2.0 Hz, 6-H, 23-H), 4.75 (s, 2H, 2-H), 7.07-7.36 (m, 18H, aromat. H).
11. 2), 6.44 (d, 4H, aromat. H), 6.53 (t, 2H, aromat. H), 6.97-7.42 (m, 28H, aromat. H).
12. Bouas-Laurent H., Castellan A., Desvergne J.-P., Lapouyade R. Chem. Soc. Rev. 29:2000;43-55.
13. Bouas-Laurent H., Desvergne J.-P. Dürr H., Bouas-Laurent H., Photochromism, Molecules and Systems. 1990;561 Elsevier, Amsterdam.
14. qO), 209.7 (CO).
15. 2J=-10.2 Hz, 2-H), 7.23 (m, 12H, aromat. H), 7.52 (m, 1H, aromat. H).
16. 2), 6.39 (d, 2H, aromat. H), 6.54 (t, 1H, aromat. H), 7.31 (m, 18H, aromat. H).
17. q), 205.6 (CO).