Swiemahogins A and B, two novel limonoids from Swietenia mahogani

Tetrahedron Letters

Volumn 48, Issue 42, 2007, Pages 7480-7484

  Chen, Yu Yu ^a   Wang, Xiao Ning ^a   Fan, Cheng Qi ^a   Yin, Sheng ^a   Yue, Jian Min ^a  

^a SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

Limonoid; Meliaceae; Single crystal X ray diffraction; Swiemahogins A and B; Swietenia mahogani

Indexed keywords

LIMONOID; PLANT EXTRACT; SWIEMAHOGINS A; SWIEMAHOGINS B; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CRYSTAL STRUCTURE; MELIACEAE; PROTON NUCLEAR MAGNETIC RESONANCE; SPECTROSCOPY; STEREOCHEMISTRY; SWIETENIA MAHOGANI; X RAY DIFFRACTION;

MELIACEAE; SWIETENIA; SWIETENIA MAHAGONI;

EID: 34548810813     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.08.066     Document Type: Article

References (21)

1. Roy A., and Saraf S. Biol. Pharm. Bull. 29 (2006) 191-201
2. Mulholland D.A., Parel B., and Coombes P.H. Curr. Org. Chem. 4 (2000) 1011-1054
3. Champagne D.E., Koul O., Isman M.B., Scudder G.G.E., and Towers G.H.N. Phytochemistry 31 (1992) 377-394
4. Akhila A., and Rani K. In: Herz W., Falk H., Kirby G.W., and Moore R.E. (Eds). Progress in the Chemistry of Organic Natural Products Vol. 78 (1999), Springer, Vienna 47-149
5. Chen, S. K.; Chen, B. Y.; Li, H. Flora of China (Zhongguo Zhiwu Zhi); Science Press: Beijing, 1997; Vol. 43, pp 44-46.
6. Darziel J.M. The Useful Plants of West Tropical Africa (1937), The Crown Agents For The Colonies, London p 235
7. Saad M.M.G., Iwagawa T., Doe M., and Nakatani M. Tetrahedron 59 (2003) 8027-8033
8. Abdelgaleil S.A.M., Doe M., Morimoto Y., and Nakatani M. Phytochemistry 67 (2006) 452-458
9. 7, 470.2305).
10. Wang X.N., Yin S., Fan C.Q., Wang F.D., Lin L.P., Ding J., and Yue J.M. Org. Lett. 8 (2006) 3845-3848
11. Taylor A.R.H., and Taylor D.A.H. Phytochemistry 23 (1984) 2676-2677
12. Muholland D.A., and Iourine S.E. Phytochemistry 47 (1998) 1357-1361
13. Kehrli A.R.H., Taylor D.A.H., and Niven M. Phytochemistry 29 (1990) 153-159
14. Mulholland D.A., Nair J.J., and Taylor D.A.H. Phytochemistry 42 (1996) 1239
15. w = 0.1162) and GOF = 1.009 for all unique reflections and S = 1.009. Crystallographic data for 1 have been deposited in the Cambridge Crystallographic Data Centre with the deposition numbers of CCDC 647896. Copies of these data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB21EZ, UK; fax: +44 1223 336 033; or e-mail: deposit@ccdc.cam.ac.uk).
16. 13Na, 615.2054).
17. Mitsui K., Maejima M., Fukaya H., Hitotsuyanagi Y., and Takeya K. Phytochemistry 65 (2004) 3075-3081
18. Muholland D.A., and Taylor D.A.H. Phytochemistry 31 (1992) 4163-4166
19. Mallavarapu G.R., Muralikrishna E., and Connolly J.D. Phytochemistry 24 (1985) 305-307
20. Niven M.L., and Taylor D.A.H. Phytochemistry 27 (1988) 1542
21. Coombes P.H., Muholland D.A., and Randrianarivelojosia M. J. Nat. Prod. 66 (2003) 735-738