Metabolites from the endophytic fungus Nodulisporium sp. from Juniperus cedre

European Journal of Organic Chemistry

Volumn , Issue 15, 2006, Pages 3498-3506

  Dai, Jingqiu ^a   Krohn, Karsten ^a   Flörke, Ulrich ^a   Draeger, Siegfried ^b   Schulz, Barbara ^b   Kiss Szikszai, Attila ^c   Antus, Sándor ^d   Kurtán, Tibor ^d   Van Ree, Teunis ^e  

^a UNIVERSITY OF PADERBORN   (Germany)

^b TECHNICAL UNIVERSITY OF BRAUNSCHWEIG   (Germany)

^c INSTITUTE OF EXPERIMENTAL MEDICINE   (Hungary)

^d UNIVERSITY OF DEBRECEN   (Hungary)

^e UNIVERSITY OF VENDA   (South Africa)

Author keywords

CD spectral analysis; Fungal metabolites; Nodulisporins A C; Nodulisporium sp.; Structural elucidation

Indexed keywords

EID: 33746522324     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200600261     Document Type: Article

References (21)

1. B. Schulz, C. Boyle, S. Draeger, H.-J. Aust, A.-K. Römmert, K. Krohn, Mycolog. Res. 2002, 996-1004.
2. A. Arnoldi, Synthesis 1984, 856-859.
3. H. R. Huang, X.-L. Feng, Z.-G. She, Y.-C. Lin, L. L. P. Vrijmoed, E. B. G. Jones, Acta Crystallogr., Sect. E 2005, 61, 282-283.
4. L. E. Gray, H. W. Gardner, D. Weisleder, M. Leib, Phytochemistry 1999, 50, 1337-1340.
5. H. Anke, V. Stadler, A. Mayer, O. Sterner, Can. J. Botany 1995, 73, 932-939(Suppl. 1, Sect. E-H, Fifth International Mycological Congress, Sect. E-H, 1994);
6. Chem. Abst. 1996, 124, 170094.
7. T. Hashimoto, S. Tahara, S. Takaoka, M. Tori, Y. Asakawa, Chem. Pharm. Bull 1994, 42, 1528-1530.
8. G. K. Poch, J. B. Gloer, J. Nat. Prod. 1989, 52, 257-260.
9. J. P. Chavez, O. R. Gottlieb, M. Yoshida, Phytochemistry 1995, 39, 849-852.
10. G. Goulston, E. I. Mercerl, J. Goad, Phytochemistry 1975, 14, 457-462.
11. M. D. Greca, L. Mangoni, A. Molinaro, P. Monaco, L. Previtera, Gazz. Chim. Ital. 1990, 120, 391-392.
12. T.-S. Wu, C.-Y. Li, Y-L. Leu, C.-Q. Hu, Phytochemistry 1999, 50, 509-512.
13. C. Dimitriadis, M. Gill, M. F. Harte, Tetrahedron 1997, 8, 2153-2158.
14. G. Snatzke, Tetrahedron 1965, 21, 439.
15. W. Gaffield, Tetrahedron 1970, 26, 4093-4108.
16. W. J. McGahren, G. A. Ellestad, G. O. Morton, M. P. Kunstman, J. Org. Chem. 1972, 37, 1636-1639.
17. M. Stadler, M. Baumgartner, T. Grothe, A. Muehlbauer, S. Seip, H. Wollweber, Phytochemistry 2001, 56, 787-793.
18. J. Dai, K. Krohn, D. Gehle, I. Kock, U. Flörke, H.-J. Aust, S. Draeger, B. Schulz, J. Rheinheimer, Eur. J. Org. Chem. 2005, 4009-4016.
19. K. Krohn, U. Flörke, M. S. Rao, K. Steingröver, H.-J. Aust, S. Draeger, B. Schulz, Nat. Prod Lett. 2001, 15, 353-361.
20. CCDC-298293 and -276512 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
21. Bruker (2002). SMART (Ver. 5.62), SAINT (Ver. 6.02), SHELXTL (Ver. 6.10) and SADABS (Version 2.03). Bruker AXS Inc., Madison, Wisconsin, USA.