2,6-Cyclo-xenicanes from the brown algae Dilophus fasciola and Dilophus spiralis

Tetrahedron

Volumn 65, Issue 51, 2009, Pages 10565-10572

  Ioannou, Efstathia ^a   Zervou, Maria ^b   Ismail, Amel ^c   Ktari, Leila ^c   Vagias, Constantinos ^a   Roussis, Vassilios ^a  

^a UNIVERSITY OF ATHENS   (Greece)

^b INSTITUTE OF BIOLOGY   (Greece)

^c INSTITUT NATIONAL DES SCIENCES ET TECHNOLOGIES DE LA MER   (Tunisia)

Author keywords

2,6 cyclo Xenicanes; Dilophus fasciola; Dilophus spiralis; Molecular modelling

Indexed keywords

2,6 CYCLO 1(9),13 XENICADIENE 18,19 DIAL; 2,6 CYCLOXENICANE; 7 HYDROXY 2,6 CYCLO 1(9),13 XENICADIENE 18,19 DIAL; 7,13 DIHYDROXY 2,6 CYCLO 1(9),14 XENICADIENE 18,19 DIAL; DITERPENE; NATURAL PRODUCT; UNCLASSIFIED DRUG;

ARTICLE; BROWN ALGA; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; DILOPHUS FASCIOLA; DILOPHUS SPIRALIS; DRUG ISOLATION; FAST ATOM BOMBARDMENT MASS SPECTROMETRY; INFRARED SPECTROSCOPY; MOLECULAR MODEL; NONHUMAN; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ANALYSIS; ULTRAVIOLET SPECTROSCOPY;

DILOPHUS (PHAEOPHYCEAE); DILOPHUS SPIRALIS; FASCIOLA; PHAEOPHYCEAE;

EID: 70449706319     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.10.081     Document Type: Article

References (18)

1. Blunt J.W., Copp B.R., Hu W.-P., Munro M.H.G., Northcote P.T., and Prinsep M.R. Nat. Prod. Rep. 26 (2009) 170-244 and earlier reviews in this series
2. MarinLit database, Department of Chemistry, University of Canterbury: http://www.chem.canterbury.ac.nz/marinlit/marinlit.shtml.
3. Blount J.F., Dunlop R.W., Erickson K.L., and Wells R.J. Aust. J. Chem. 35 (1982) 145-163
4. Enoki N., Ishida R., and Matsumoto T. Chem. Lett. (1982) 1749-1752
5. Ishitsuka M., Kusumi T., Tanaka J., Chihara M., and Kakisawa H. Chem. Lett. (1984) 151-154
6. Ishitsuka M., Kusumi T., Kakisawa H., Kawakami Y., Nagai Y., and Sato T. Tetrahedron Lett. 24 (1983) 5117-5120
7. Kashman Y., and Groweiss. J. Org. Chem. 45 (1980) 3814-3824
8. Kodama M., Okumura K., Kobayashi Y., Tsunoda T., and Ito S. Tetrahedron Lett. 25 (1984) 5781-5784
9. Ishitsuka M., Kusumi T., Kakisawa H., Kawakami Y., Nagai Y., and Sato T. Tetrahedron Lett. 27 (1986) 2639-2642
10. Sims J.J., and Pettus Jr. J.A. Phytochemistry 15 (1976) 1076-1077
11. Brown G.D. Phytochemistry 36 (1994) 1553-1554
12. Nes W.R., Castle M., McClanahan J.L., and Settine J.M. Steroids 8 (1966) 655-657
13. Frost D.J., and Ward J.P. Tetrahedron Lett. 9 (1968) 3779-3782
14. Haugan J.A., and Liaaen-Jensen S. Phytochemistry 31 (1992) 1359-1361
15. Haugan J.A., and Liaaen-Jensen S. Tetrahedron Lett. 35 (1994) 2245-2248
16. Danise B., Minale L., Riccio R., Amico V., Oriente G., Piattelli M., Tringali C., Fattorusso E., Magno S., and Mayol L. Experientia 33 (1977) 413-415
17. Ishitsuka M., Kusumi T., and Kakisawa H. Tetrahedron Lett. 23 (1982) 3179-3180
18. König G.M., Wright A.D., and Sticher O. Phytochemistry 30 (1991) 3679-3682