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Volumn 1, Issue 2, 1999, Pages 337-340

Isolation, structure elucidation, and synthesis of bisgersolanolide, a novel heptacyclic bis-diterpenoid from the gorgonian octocoral Pseudopterogorgia bipinnata

Author keywords

[No Author keywords available]

Indexed keywords

BISGERSOLANOLIDE; FUSED HETEROCYCLIC RINGS;

EID: 0033614858     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol990660c     Document Type: Article
Times cited : (32)

References (18)
  • 2
    • 0032054664 scopus 로고    scopus 로고
    • and previous papers in this series
    • Faulkner, D. J. Nat. Prod. Rep. 1998, 15, 113-158 and previous papers in this series.
    • (1998) Nat. Prod. Rep. , vol.15 , pp. 113-158
    • Faulkner, D.J.1
  • 7
    • 0042075500 scopus 로고    scopus 로고
    • note
    • Spectral data for bisgersolanolide (1) have been deposited as Supporting Information.
  • 12
    • 0344681596 scopus 로고
    • 20 skeletons. On structural grounds, the majority of these bis-diterpenes appear to be derived from a classical Diels-Alder reaction of a diterpenoid diene with an activated dienophile-containing diterpenoid precursor. For well-documented examples, see: (a) Falshaw, C. P.; King, T. J. J. Chem. Soc., Perkin Trans. 1 1983, 1749-1752.
    • (1983) J. Chem. Soc., Perkin Trans. 1 , pp. 1749-1752
    • Falshaw, C.P.1    King, T.J.2
  • 17
    • 0042576519 scopus 로고    scopus 로고
    • note
    • If either the diene or the dienophile is chiral and optically active, facially selective addition will give rise to a nonstatistical mixture of optically active diastereomers.
  • 18
    • 0001147462 scopus 로고
    • Cycloaddition reactions in organic synthesis
    • Baldwin, J. E., Magnus, P. D., Eds.; Pergamon Press: London
    • Carruthers, W. Cycloaddition Reactions in Organic Synthesis. In Tetrahedron Organic Chemistry Series; Baldwin, J. E., Magnus, P. D., Eds.; Pergamon Press: London, 1990; Vol. 8, pp 1-90.
    • (1990) Tetrahedron Organic Chemistry Series , vol.8 , pp. 1-90
    • Carruthers, W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.