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Volumn , Issue 33, 2009, Pages 5711-5715

Iso-seco-tanapartholides: Isolation, synthesis and biological evaluation

Author keywords

Cleavage reaction; Inflammation; Natural products; Terpenoids; Total synthesis

Indexed keywords


EID: 72849150191     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200901016     Document Type: Article
Times cited : (31)

References (33)
  • 12
    • 0000011138 scopus 로고
    • Iso-seco-tanapartholide was assigned structure 1, see
    • a) Iso-seco-tanapartholide was assigned structure 1, see: S. Huneck, C. Zdero, F. Bohlmann, Phytochemistry 1986, 25, 883-889;
    • (1986) Phytochemistry , vol.25 , pp. 883-889
    • Huneck, S.1    Zdero, C.2    Bohlmann, F.3
  • 18
    • 72849140033 scopus 로고    scopus 로고
    • See Supporting Information for further details
    • See Supporting Information for further details.
  • 19
    • 72849140570 scopus 로고    scopus 로고
    • It was also confirmed that the active fraction did not target the reporter protein, firefly luciferase, by using an in vitro assay (data not shown)
    • It was also confirmed that the active fraction did not target the reporter protein, firefly luciferase, by using an in vitro assay (data not shown).
  • 24
    • 72849133410 scopus 로고    scopus 로고
    • [8] contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • [8] contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 26
    • 84971046730 scopus 로고
    • It cannot be ruled out that lead tetraacetate rapidly cleaves 7 and 25 without forming a cyclic ester intermediate and that the speed of the reaction results from release of steric congestion on. cleavage of the Cl-C10 bond. We thank a reviewer for raising this possibility
    • R. Criegee, E. Hoger, G. Huber, P. Kruck, F. Marktscheffel, H. Schellenberger, Justus Liebigs Ann. Chem. 1956, 599, 81-125. It cannot be ruled out that lead tetraacetate rapidly cleaves 7 and 25 without forming a cyclic ester intermediate and that the speed of the reaction results from release of steric congestion on. cleavage of the Cl-C10 bond. We thank a reviewer for raising this possibility.
    • (1956) Justus Liebigs Ann. Chem. , vol.599 , pp. 81-125
    • Criegee, R.1    Hoger, E.2    Huber, G.3    Kruck, P.4    Marktscheffel, F.5    Schellenberger, H.6
  • 27
    • 72849141994 scopus 로고    scopus 로고
    • In this reaction a compound tentatively assigned as the C3 oxo derivative of I. was formed
    • In this reaction a compound tentatively assigned as the C3 oxo derivative of I. was formed.
  • 28
    • 72849129860 scopus 로고    scopus 로고
    • 3)
    • 3).
  • 29
    • 72849153064 scopus 로고    scopus 로고
    • This sample was kindly provided by Professor Todorova. For example, and references cited therein
    • This sample was kindly provided by Professor Todorova. For example, see M. Todorova, E. Mustakerova, E. Tsankova, Dokl. Bulg. Akad. Nauk. 2005, 58, 25-32 and references cited therein.
    • (2005) Dokl. Bulg. Akad. Nauk , vol.58 , pp. 25-32
    • Todorova, M.1    Mustakerova, E.2    Tsankova, E.3
  • 30
    • 4344592673 scopus 로고    scopus 로고
    • For previous reports on the biological activity of this family of natural products, see: a
    • For previous reports on the biological activity of this family of natural products, see: a) H. Z. Jin, J. H. Lee, D. Lee, Y. S. Hong, Y. H. Kim, J. J. Lee, Phytochemistry 2004, 65, 2247-2253;
    • (2004) Phytochemistry , vol.65 , pp. 2247-2253
    • Jin, H.Z.1    Lee, J.H.2    Lee, D.3    Hong, Y.S.4    Kim, Y.H.5    Lee, J.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.