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Volumn , Issue 24, 1996, Pages 2717-2718

Enantiospecific total synthesis of (+)- and (-)-avarone and -avarol

Author keywords

[No Author keywords available]

Indexed keywords

ANTIVIRUS AGENT; AVAROL; AVARONE;

EID: 0030463134     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/CC9960002717     Document Type: Article
Times cited : (25)

References (27)
  • 1
    • 0026177349 scopus 로고
    • For a review of drimane sesquiterpenoids and their biological activities see: B. J. M. Jansen and A. de Groot, Nat. Prod. Rep., 1991, 309; M. L. Bourguet-Konracki, A. Longeon, E. Morel and M. Guyot, Int. J. Immunopharmac., 1991, 13, 393; W. E. G. Müller, R. K. Zahn, M. J. Gasic, N. Dogovic, A. Maidhof, C. Becker, B. Diehl-Seifert and E. Eich, Comp. Biochem. Physiol., 1985, 80C, 47.
    • (1991) Nat. Prod. Rep. , pp. 309
    • Jansen, B.J.M.1    De Groot, A.2
  • 2
    • 0025909786 scopus 로고
    • For a review of drimane sesquiterpenoids and their biological activities see: B. J. M. Jansen and A. de Groot, Nat. Prod. Rep., 1991, 309; M. L. Bourguet-Konracki, A. Longeon, E. Morel and M. Guyot, Int. J. Immunopharmac., 1991, 13, 393; W. E. G. Müller, R. K. Zahn, M. J. Gasic, N. Dogovic, A. Maidhof, C. Becker, B. Diehl-Seifert and E. Eich, Comp. Biochem. Physiol., 1985, 80C, 47.
    • (1991) Int. J. Immunopharmac. , vol.13 , pp. 393
    • Bourguet-Konracki, M.L.1    Longeon, A.2    Morel, E.3    Guyot, M.4
  • 7
    • 0016816965 scopus 로고
    • G. Cimino, S. De Stefano and L. Minale, Experientia, 1975, 31, 1117; G. Cimino, S. De Stefano, W. Fenical, L. Minale and L. Sims, Experientia, 1975, 31, 1250.
    • (1975) Experientia , vol.31 , pp. 1117
    • Cimino, G.1    De Stefano, S.2    Minale, L.3
  • 18
    • 0001220638 scopus 로고
    • C. Agami, F. Meynier, C. Puchot, J. Guilhem and C. Pascard, Tetrahedron, 1984, 40, 1031. For a slightly different procedure see, R. Uma, S. Swaminathan and K. Rajagopalan, Tetrahedron Lett., 1984, 25, 5825; H. Hagiwara and H. Uda, J. Org. Chem., 1988, 53, 2308.
    • (1984) Tetrahedron , vol.40 , pp. 1031
    • Agami, C.1    Meynier, F.2    Puchot, C.3    Guilhem, J.4    Pascard, C.5
  • 19
    • 0001357129 scopus 로고
    • C. Agami, F. Meynier, C. Puchot, J. Guilhem and C. Pascard, Tetrahedron, 1984, 40, 1031. For a slightly different procedure see, R. Uma, S. Swaminathan and K. Rajagopalan, Tetrahedron Lett., 1984, 25, 5825; H. Hagiwara and H. Uda, J. Org. Chem., 1988, 53, 2308.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 5825
    • Uma, R.1    Swaminathan, S.2    Rajagopalan, K.3
  • 20
    • 33845279247 scopus 로고
    • C. Agami, F. Meynier, C. Puchot, J. Guilhem and C. Pascard, Tetrahedron, 1984, 40, 1031. For a slightly different procedure see, R. Uma, S. Swaminathan and K. Rajagopalan, Tetrahedron Lett., 1984, 25, 5825; H. Hagiwara and H. Uda, J. Org. Chem., 1988, 53, 2308.
    • (1988) J. Org. Chem. , vol.53 , pp. 2308
    • Hagiwara, H.1    Uda, H.2
  • 27
    • 0028948656 scopus 로고
    • A total synthesis of the sesquiterpene ilimaquinone, which also possesses interesting biological activity, has been reported recently. See S. D. Bruner, H. S. Radeke, J. A. Tallarico and M. L. Snapper, J. Org. Chem., 1995, 60, 1114.
    • (1995) J. Org. Chem. , vol.60 , pp. 1114
    • Bruner, S.D.1    Radeke, H.S.2    Tallarico, J.A.3    Snapper, M.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.