Synthesis of C-seco limonoid model insect antifeedants related to ochinolide

Synlett

Volumn , Issue 12, 1998, Pages 1372-1374

  Fernandez Mateos A ^a   Martin De La Nava E ^a   Pascual Coca, G ^a   Ramos Silvo, A ^a   Rubio Gonzalez R ^a  

^a UNIVERSITY OF SALAMANCA   (Spain)

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[No Author keywords available]

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EID: 0002837979     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (18)

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2. b) Champagne, D. E.; Koul, O.; Isman, M. B.; Scuddcr, G. G. E.; Towers, G. H. N. Phytochemistry 1992, 31, 377.
3. Ley, S. V.; Denholm, A. A.; Wood, A. Nat. Prod. Rep. 1993, 109-157.
4. a) Kraus, W. Biologically active compounds from Meliaceae. In Chemistry and Biotechnology of Biologically Active Natural Products; Proceedings of the Second International Conference; Budapest, 15-19 August, 1983. Szantay, Cs., Chemistry. 17; Elservier: Amsterdam, 1984; pp 331-345.
5. b) Rajab, M. S.; Bentley, M. D.; Fort, Jr R. C.; J. Nat. Prod.
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8. (a) Santelli-Rouvier, C.; Santelli, M. Synthesis 1983, 429.
9. (b) Habermas, K. L.; Denmark, S.E.; Jones, T. K. Org. Reactions 1994, 45, 1.
10. Ref 1a) pp 33-35.
11. All compounds synthetized are racemic although, only one enantiomer is depicted.
12. Marino, J. P.; Linderman, R. J. J. Org. Chem. 1981, 46, 3696.
13. Edwars, B. E.; Rao, P. N. J. Org. Chem. 1966, 31, 324.
14. 4.
15. Buchanan, G. L.; Young, G. A. R. J. Chem. Soc., Chem. Commun. 1971, 643.
16. Corey, E. J.; Nicolaou, K. C. J. Am. Chem. Soc. 1974, 96, 5694.
17. Freimanis, J.; Bokaldere, R.; Lola, D.; Turovskii, I. V.; Gavais, M. Zh. Org. Khim. 1990, 26, 1114.
18. The structure assigned to compounds 6a, 6b, 11 and 11a has been determined by H-C correlations and NOE experiments. Selected NOE % values are