Structural and spectral assignment by two-dimensional NMR of two new derivatives of the abietane diterpenoid taxodione

Magnetic Resonance in Chemistry

Volumn 43, Issue 1, 2005, Pages 97-99

  Rodríguez, Benjamín ^a  

^a INSTITUTO DE QUÍMICA ORGÁNICA GENERAL   (Spain)

Author keywords

7 methoxytaxodione; 13C NMR; 1H NMR; Abietane diterpenoids; Homo cyclopropane derivative; NMR; Taxodione; Two dimensional NMR

Indexed keywords

LIPIDS; MASS SPECTROMETRY;

13C NMR; 1H NMR; 7-METHOXYTAXODIONE; ABIETANE DITERPENOID; CYCLOPROPANE DERIVATIVE; DITERPENOIDS; HOMO-CYCLOPROPANE DERIVATIVE; STRUCTURAL ASSIGNMENTS; TAXODIONE; TWO-DIMENSIONAL NMR;

NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

7 METHOXYTAXODIONE; ABIETANE DERIVATIVE; DIAZOMETHANE; DITERPENOID; TAXODIONE; UNCLASSIFIED DRUG; DITERPENE;

ARTICLE; DRUG STRUCTURE; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STRUCTURE ANALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; METHODOLOGY;

DITERPENES; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; MOLECULAR CONFORMATION;

EID: 16644393009     PISSN: 07491581     EISSN: None     Source Type: Journal    
DOI: 10.1002/mrc.1503     Document Type: Article

References (22)

1. Connolly JD, Hill RA. Dictionary of Terpenoids, vol. 2. Chapman & Hall: London, 1991.
2. Hanson JR. Nat. Prod. Rep. 2000; 17: 165;
3. Nat. Prod. Rep. 2001; 18: 88;
4. Nat. Prod. Rep. 2002; 19: 125;
5. Nat. Prod. Rep. 2003; 20: 70;
6. Nat. Prod. Rep. 2004; 21: 312.
7. Cousins DJ. Medicinal, Essential Oil, Culinary Herb and Pesticidal Plants of the Labiatae, Parts 1 and 2. CAB International: Wallingford, 1994.
8. Kupchan SM, Karim A, Marcks C. J. Org. Chem. 1969; 34: 3912.
9. Hueso-Rodríguez JA, Jimeno ML, Rodríguez B, Savona G, Bruno M. Phytochemistry 1983; 22: 2005.
10. Rodríguez B. Z. Naturforsch. 2002; 58b: 324.
11. Tezuka Y, Kasimu R, Li JX, Basnet P, Tanaka K, Namba T, Kadota S. Chem. Pharm. Bull. 1998; 46: 107.
12. Haslinger E, Michl G. Liebigs Ann. Chem. 1989; 677.
13. Engler TA, Sampath U, Naganathan S, Velde DV, Takusagawa F, Yohannes D. J. Org. Chem. 1989; 54: 5712.
14. Harring SR, Livinghouse T. J. Chem. Soc., Chem. Commun. 1992; 502.
15. Sánchez AJ, Konopelski JP. Synlett 1994; 335.
16. Stevens RV, Bisacchi GS. J. Org. Chem. 1982; 47: 2396.
17. Rodríguez B. Magn. Reson. Chem. 2003; 41: 741.
18. Marletti F, delle Monache F, Marini-Bettolo GB, de Araujo MCM, Cavalcanti MSB, D'Albuquerque IL, de Lima OG. Gazz. Chim. Ital. 1976; 106: 119.
19. Wenkert E, Fuchs A, McChesney JD. J. Org. Chem. 1965; 30: 2931.
20. González AG, Andrés LS, Herrera JR, Luis JG, Ravelo AG. Can. J. Chem. 1989; 67: 208.
21. González AG, Andrés LS, Aguiar ZE, Luis JG. Phytochemistry 1992; 31: 1297.
22. Gutsche CD. In Organic reactions, vol. VIII, Adams R (ed.). John Wiley: New York, 1954; chapt. 8.