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Volumn , Issue 16, 2000, Pages 2933-2938

Epoxidation studies on lathyra-6(17),12-dienes - Revised structure of the Euphorbia Factor L1

Author keywords

Diterpenes; Epoxidations; Euphorbia Factor L1; Lathyrol; Natural products; Structure elucidations

Indexed keywords

ALKADIENE; DITERPENOID; MACROCYCLIC COMPOUND; NATURAL PRODUCT;

EID: 0033848761     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200008)2000:16<2933::AID-EJOC2933>3.0.CO;2-J     Document Type: Article
Times cited : (21)

References (25)
  • 4
    • 0021741668 scopus 로고
    • An anionic process involving the intramolecular aldol reaction of a lathyra-7,14-dione has been proposed. Though a synthetic mimic of this process could be achieved, the observed configuration and oxygenation pattern at the cyclopentane ring junction (C-4 and C-15, lathyrane numbering, corresponding to C-4 and C-10 of the tigliane skeleton) was opposite to that observed in natural tiglianes, suggesting a more subtle mechanism (Y. Shizuri, J. Ohtsuka, S. Kosemura, Y. Terada, S. Yamamura, Tetrahedron Lett. 1984, 25, 5547-5550).
    • (1984) Tetrahedron Lett. , vol.25 , pp. 5547-5550
    • Shizuri, Y.1    Ohtsuka, J.2    Kosemura, S.3    Terada, Y.4    Yamamura, S.5
  • 7
    • 85027475123 scopus 로고
    • Y. Tahara, Chem. Ber. 1890, 23, 3347-3351.
    • (1890) Chem. Ber. , vol.23 , pp. 3347-3351
    • Tahara, Y.1
  • 10
    • 0001669823 scopus 로고
    • 1 was also isolated in trace amounts (0.3 ppm) from the Chinese plant Macaranga tanarius Muell. Arg. (W.-H. Hui, M.-M. Li, K.-K. Ng, Phytochemistry 1975, 14, 816-817).
    • (1975) Phytochemistry , vol.14 , pp. 816-817
    • Hui, W.-H.1    Li, M.-M.2    Ng, K.-K.3
  • 17
    • 77957038732 scopus 로고
    • (Eds.: V. Farina), Elsevier, Amsterdam
    • For a discussion of this issue in the context of the two-dimensional representation of the taxane skeleton, see: [13a] G. Appendino, In The Chemistry and Pharmacology of Taxol and its Derivatives (Eds.: V. Farina), Elsevier, Amsterdam, 1995, pp. 55-58. [13b] N. H. Fischer, E. J. Olivier, H. D. Fischer, in: Progress in the Chemistry of Organic Natural Products (Eds.: W. Herz, H. Grisebach, G. W. Kirby), Springer, Wien, 1979, vol. 38, pp. 59-60.
    • (1995) The Chemistry and Pharmacology of Taxol and Its Derivatives , pp. 55-58
    • Appendino, G.1
  • 18
    • 0002058708 scopus 로고
    • (Eds.: W. Herz, H. Grisebach, G. W. Kirby), Springer, Wien
    • For a discussion of this issue in the context of the two-dimensional representation of the taxane skeleton, see: [13a] G. Appendino, In The Chemistry and Pharmacology of Taxol and its Derivatives (Eds.: V. Farina), Elsevier, Amsterdam, 1995, pp. 55-58. [13b] N. H. Fischer, E. J. Olivier, H. D. Fischer, in: Progress in the Chemistry of Organic Natural Products (Eds.: W. Herz, H. Grisebach, G. W. Kirby), Springer, Wien, 1979, vol. 38, pp. 59-60.
    • (1979) Progress in the Chemistry of Organic Natural Products , vol.38 , pp. 59-60
    • Fischer, N.H.1    Olivier, E.J.2    Fischer, H.D.3
  • 19
    • 6744231057 scopus 로고    scopus 로고
    • note
    • The Chemical Abstract name for epoxylathyrol is [1aR-(1aR*, 2E,4aR*,6S*7S*,7aR*,8S*,9R*,11aS*)]- 1a,4a,5,6,7,7a,8, 10,11,11a-Decahydro-4a,7,8-trihydroxy-1,1,3,6-tetramethylspiro-[9H-cyclopenta[a] cyclopropa[f]cycloundecene-9,2′-oxiran]4H(1H)-one.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.