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Volumn 65, Issue 36, 2009, Pages 7449-7456

Stereoselective synthesis and absolute configuration of the C33-C42 fragment of symbiodinolide

Author keywords

Absolute configuration; Chemical synthesis; Cross metathesis degradation; Symbiodinolide

Indexed keywords

ALPHA METHOXY ALPHA(TRIFLUOROMETHYL)PHENYLACETYL DERIVATIVE; ASPARTIC ACID; ETHYLENE; MACROLIDE; PHENYLACETIC ACID DERIVATIVE; SYMBIODINOLIDE; UNCLASSIFIED DRUG;

EID: 67949088341     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.07.019     Document Type: Article
Times cited : (23)

References (42)
  • 1
    • 0039820322 scopus 로고
    • Scheuer P.J. (Ed), Springer, Berlin, Heidelberg
    • Uemura D. In: Scheuer P.J. (Ed). Bioorganic Marine Chemistry Vol. 4 (1991), Springer, Berlin, Heidelberg 1-31
    • (1991) Bioorganic Marine Chemistry , vol.4 , pp. 1-31
    • Uemura, D.1
  • 5
    • 0034122087 scopus 로고    scopus 로고
    • and references cited therein
    • Murata M., and Yasumoto T. Nat. Prod. Rep. 17 (2000) 293-314 and references cited therein
    • (2000) Nat. Prod. Rep. , vol.17 , pp. 293-314
    • Murata, M.1    Yasumoto, T.2
  • 7
    • 67949096901 scopus 로고    scopus 로고
    • Symbiodinolide (1) is a structural congener of zooxanthellatoxins which are polyol macrolides isolated from the dinoflagellate Symbiodinium sp. For the structural elucidation of zooxanthellatoxins, see:
    • Symbiodinolide (1) is a structural congener of zooxanthellatoxins which are polyol macrolides isolated from the dinoflagellate Symbiodinium sp. For the structural elucidation of zooxanthellatoxins, see:
  • 19
    • 67949103049 scopus 로고    scopus 로고
    • note
    • For a preliminary communication, see Ref. 5b.
  • 25
    • 67949084578 scopus 로고    scopus 로고
    • note
    • Structural determination of other degraded products obtained by cross-metathesis will be reported in the near future.
  • 27
    • 18744369934 scopus 로고    scopus 로고
    • For determination of the absolute stereochemistry of secondary/secondary diols by the modified Mosher method, see:
    • For determination of the absolute stereochemistry of secondary/secondary diols by the modified Mosher method, see:. Freire F., Seco J.M., Quiñoá E., and Riguera R. J. Org. Chem. 70 (2005) 3778-3790
    • (2005) J. Org. Chem. , vol.70 , pp. 3778-3790
    • Freire, F.1    Seco, J.M.2    Quiñoá, E.3    Riguera, R.4
  • 30
    • 67949083047 scopus 로고    scopus 로고
    • note
    • The absolute configuration of 6 was unambiguously confirmed by the modified Mosher method.
  • 36
    • 67949089188 scopus 로고    scopus 로고
    • note
    • The absolute stereochemistry at the resulting chiral center of 11 was determined by the modified Mosher method.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.