Syntheses, characterization and fluorescent properties of two series of dehydroabietic acid C-ring derivatives

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy

Volumn 76, Issue 3-4, 2010, Pages 328-335

  Wang, Yingchun ^a,b   Su, Chunhua ^a   Li, Fangyao ^a   Liu, Luzhi ^a   Pan, Yingming ^a   Wu, Xiurong ^a   Wang, Hengshan ^a  

^a GUANGXI NORMAL UNIVERSITY   (China)

^b JISHOU UNIVERSITY   (China)

Author keywords

Absorption; Dehydroabietic acid; Fluorescence; Quantum yields

Indexed keywords

ABSORPTION AND EMISSION SPECTRA; AROMATIC RINGS; DEHYDROABIETIC ACID; ELEMENT ANALYSIS; FLUORESCENCE QUANTUM YIELD; FLUORESCENT PROPERTY; NITROGEN-CONTAINING HETEROCYCLES; PLANAR STRUCTURE; RING DERIVATIVES; SPECTRAL CHARACTERISTICS; SUBSTITUTED COMPOUNDS; UV-VIS ABSORPTIONS;

ABSORPTION; ACIDS; BENZENE; EMISSION SPECTROSCOPY; QUANTUM YIELD; RIGID STRUCTURES;

FLUORESCENCE;

ABIETANE DERIVATIVE; DEHYDROABIETIC ACID; FLUORESCENT DYE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; INFRARED SPECTROPHOTOMETRY; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SPECTROFLUOROMETRY; SYNTHESIS; ULTRAVIOLET SPECTROPHOTOMETRY;

DITERPENES, ABIETANE; FLUORESCENT DYES; MAGNETIC RESONANCE SPECTROSCOPY; MASS SPECTROMETRY; MOLECULAR STRUCTURE; SPECTROMETRY, FLUORESCENCE; SPECTROPHOTOMETRY, INFRARED; SPECTROPHOTOMETRY, ULTRAVIOLET;

EID: 77953290947     PISSN: 13861425     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.saa.2010.03.014     Document Type: Article

References (30)

1. Gigante B., Santos C., and Silva A.M. Bioorg. Med. Chem. 11 (2003) 1631
2. Esteves A.M., and Narender N. J. Nat. Prod. 64 (2001) 761
3. Wade H., Kodato S.I., Kawamori M., and Morikawa T. Chem. Pharm. Bull. 33 (1985) 1472
4. Feio S.S., Gigante B., and Roseiro J.C. J. Microbiol. Methods 28 (1997) 201
5. Feio S.S., Gigante B., and Roseiro J.C. J. Microbiol. Methods 35 (1999) 215
6. Gigante B., Santos C., Silva A.M., Curto M.J.M., and Nascimento M.S.J. Bioorg. Med. Chem. 11 (2003) 1631
7. Fonseca T., and Gigante B. Bioorg. Med. Chem. 12 (2004) 103
8. Beatriz S., and Guillermo S.H. Pharm. Res. 52 (2005) 29
9. Matsusushita Y., Iwakiri Y., and Yoshida S. Tetrahedron Lett. 46 (2005) 3629
10. Matsumoto T., and Takeda Y. Chem. Pharm. Bull. 44 (1996) 1583
11. Tayana B.K., Nikalai N.K., Olga V.T., and Alexander G.T. Chirality 16 (2004) 40
12. Alexander G.T., Olga V.T., Tayana B.K., and Nikalai N.K. Chem. Comp. Simult. Butlerov. Commun. 7 (2002) 1
13. Zhao S.L., Wang H.S., Pan Y.M., and He M. J. Chromatogr. A 1145 (2007) 246
14. Wang H.S., Zhao S.L., He M., Zhao Z.C., and Pan Y.M. J. Sep. Sci. 30 (2007) 2748
15. Zhao S.L., Zhang R.C., Wang H.S., Tang L.D., and Pan Y.M. J. Chromatogr. B 833 (2006) 186
16. Wang H.S., Zhang R.C., Zhao S.L., Tang L.D., and Pan Y.M. Anal. Chim. Acta 560 (2006) 64
17. Ma H.M., Wang Z.H., and Su M.H. J. Chromatogr. A 955 (2002) 125
18. Casu M.B., Imperia P., and Schrader S. Synth. Met. 121 (2001) 1397
19. Burrows H.D., Fonseca S.M., Gigante B., Esteves M.A., and Guerreiro A.M. J. Fluoresc. 16 (2006) 227
20. Bernardo G., Esteves M.A., Guerreiro A.M., Gigante B., and Morgado J. Opt. Mater. 31 (2008) 320
21. Ramachandram B., Sankaran N., Karmaber R., Saha S., and Samanta A. Tetrahedron 56 (2000) 7041
22. Wang P., Xie Z., and Wong O. Chem. Mater. 15 (2003) 1913
23. Zhu W., Fan L., and Yao R. Synth. Met. 137 (2003) 1129
24. Birks J.B., and Dyson D.J. Proc. Roy. Soc. A 275 (1963) 135
25. Halbrook N.J., and Lawrence R.V. J. Org. Chem. 31 (1966) 4246
26. Tahara A., Akita H., and Yasuo O. Chem. Pharm. Bull. 22 (1974) 1547
27. Fieser F.L., and Campbell W.P. J. Chem. Soc. C 61 (1939) 2528
28. Hazelton J.C., Iddon B., Suschitzky H., and Woolley L.H. Tetrahedron 51 (1995) 10771
29. Wang H.S., Wang Y.C., and Pan Y.M. Tetrahedron Lett. 49 (2008) 2634
30. Silvestre A.J.D., Monteiro S.M.C., and Silva A.M.S. Monatsh. Chem. 129 (1998) 1183