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Volumn 44, Issue 30, 2003, Pages 5727-5730

Synthesis of alkylated iridolactone analogs

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL GROUP; IRIDOID; IRIDOLACTONE; LACTONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0038166587     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)01320-0     Document Type: Article
Times cited : (8)

References (30)
  • 1
    • 0010561929 scopus 로고
    • Marcel Dekker: New York
    • For reviews, see: (a) Bobitt, J. M.; Segebarth, K. P. Cyclopentanoid Terpene Derivatives; Marcel Dekker: New York, 1969; (b) Bianco, A. In Studies in Natural Products Chemistry; Rhaman, A. U., Ed.; Elsevier: Amsterdam, 1990; Vol. 7, p. 439; (c) Franzyk, H. In Progress in the Chemistry of Organic Natural Products; Herz, W.; Falk, H.; Kirby, G. W.; Moore, R. E., Eds.; Springer-Verlag: Wien, 2000; Vol. 73, pp. 1-114.
    • (1969) Cyclopentanoid Terpene Derivatives
    • Bobitt, J.M.1    Segebarth, K.P.2
  • 2
    • 0001064317 scopus 로고
    • Rhaman, A. U., Ed.; Elsevier: Amsterdam
    • For reviews, see: (a) Bobitt, J. M.; Segebarth, K. P. Cyclopentanoid Terpene Derivatives; Marcel Dekker: New York, 1969; (b) Bianco, A. In Studies in Natural Products Chemistry; Rhaman, A. U., Ed.; Elsevier: Amsterdam, 1990; Vol. 7, p. 439; (c) Franzyk, H. In Progress in the Chemistry of Organic Natural Products; Herz, W.; Falk, H.; Kirby, G. W.; Moore, R. E., Eds.; Springer-Verlag: Wien, 2000; Vol. 73, pp. 1-114.
    • (1990) Studies in Natural Products Chemistry , vol.7 , pp. 439
    • Bianco, A.1
  • 3
    • 0037569442 scopus 로고    scopus 로고
    • Herz, W.; Falk, H.; Kirby, G. W.; Moore, R. E., Eds.; Springer-Verlag: Wien
    • For reviews, see: (a) Bobitt, J. M.; Segebarth, K. P. Cyclopentanoid Terpene Derivatives; Marcel Dekker: New York, 1969; (b) Bianco, A. In Studies in Natural Products Chemistry; Rhaman, A. U., Ed.; Elsevier: Amsterdam, 1990; Vol. 7, p. 439; (c) Franzyk, H. In Progress in the Chemistry of Organic Natural Products; Herz, W.; Falk, H.; Kirby, G. W.; Moore, R. E., Eds.; Springer-Verlag: Wien, 2000; Vol. 73, pp. 1-114.
    • (2000) Progress in the Chemistry of Organic Natural Products , vol.73 , pp. 1-114
    • Franzyk, H.1
  • 4
    • 0030797910 scopus 로고    scopus 로고
    • Nangia A. Tetrahedron. 53:1997;14507-14545.
    • (1997) Tetrahedron , vol.53 , pp. 14507-14545
    • Nangia, A.1
  • 13
    • 85064412687 scopus 로고
    • For uses of the intramolecular HWE reaction for the synthesis of γ- and δ-lactones, see: (a) Mickolajczyk, M.; Midura, W. H. Synlett 1991, 245-247; (b) Nangia, A.; Rao, P. B. Tetrahedron Lett. 1992, 33, 2375-2378; (c) Nangia, A.; Prasuna, G.; Rao, P. B. Tetrahedron Lett. 1994, 35, 3755-3758.
    • (1991) Synlett , pp. 245-247
    • Mickolajczyk, M.1    Midura, W.H.2
  • 14
    • 0026575527 scopus 로고
    • For uses of the intramolecular HWE reaction for the synthesis of γ- and δ-lactones, see: (a) Mickolajczyk, M.; Midura, W. H. Synlett 1991, 245-247; (b) Nangia, A.; Rao, P. B. Tetrahedron Lett. 1992, 33, 2375-2378; (c) Nangia, A.; Prasuna, G.; Rao, P. B. Tetrahedron Lett. 1994, 35, 3755-3758.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 2375-2378
    • Nangia, A.1    Rao, P.B.2
  • 15
    • 0028264263 scopus 로고
    • For uses of the intramolecular HWE reaction for the synthesis of γ- and δ-lactones, see: (a) Mickolajczyk, M.; Midura, W. H. Synlett 1991, 245-247; (b) Nangia, A.; Rao, P. B. Tetrahedron Lett. 1992, 33, 2375-2378; (c) Nangia, A.; Prasuna, G.; Rao, P. B. Tetrahedron Lett. 1994, 35, 3755-3758.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 3755-3758
    • Nangia, A.1    Prasuna, G.2    Rao, P.B.3
  • 25
    • 85031160564 scopus 로고    scopus 로고
    • note
    • 3 (1.06 equiv.) in THF (-65°C, 5.5 h).
  • 30
    • 85031145588 scopus 로고    scopus 로고
    • note
    • 2: C, 71.02; H, 7.95. Found: C, 70.77; H, 8.12.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.