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Volumn , Issue 8, 2010, Pages 1483-1493

Synthetic studies directed towards various homologues of natural Sesquiterpene-Coumarin ethers: The Domino approach

Author keywords

Configuration determination; Galbanic acid analogues; Secodriol analogues; Terpenoids

Indexed keywords


EID: 77649214689     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200901352     Document Type: Article
Times cited : (6)

References (34)
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    • [8], named this compound marnerai (and its corresponding alcohol marnerol) in recognition of Marner's pioneering work on iridais. Marnerai has never been isolated but was hypothesized to be the first carbocyclic precursor in the biosynthesis of iridals; a
    • [8], named this compound marnerai (and its corresponding alcohol marnerol) in recognition of Marner's pioneering work on iridais. Marnerai has never been isolated but was hypothesized to be the first carbocyclic precursor in the biosynthesis of iridals; a) F.-J. Marner, W. Krick, B. Gellrich, L. Jaenicke, J. Org. Chem. 1982, 47, 2531-2538;
    • (1982) J. Org. Chem. , vol.47 , pp. 2531-2538
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    • For the revised, though erroneous, structure of galbanic acid suggested by Lee et al., see
    • For the revised, though erroneous, structure of galbanic acid suggested by Lee et al., see: S. G. Lee, S. Ryu, J. W. Ahn, Bull. Korean Chem. Soc. 1998, 19, 384-386.
    • (1998) Bull. Korean Chem. Soc. , vol.19 , pp. 384-386
    • Lee, S.G.1    Ryu, S.2    Ahn, J.W.3
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    • With the exception of the contribution reported recently by our group there appear to have been, no prior synthetic studies.
    • With the exception of the contribution reported recently by our group there appear to have been, no prior synthetic studies.
  • 21
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    • Eds.: M. Shibasaki, J. F. Stoddart, F. Vögtle, Wiley-VCH, Weinheim
    • c) L. F. Tietze, F. Haunert, in: Stimulating Concepts in Chemistry (Eds.: M. Shibasaki, J. F. Stoddart, F. Vögtle), Wiley-VCH, Weinheim, 2000, pp. 39-64;
    • (2000) Stimulating Concepts in Chemistry , pp. 39-64
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    • Eds.: L. F. Tietze, G. Brasche, K. M. Gericke, Wiley-VCH, ISBN 3-527-29060-5.
    • d) Domino Reactions in Organic Synthesis (Eds.: L. F. Tietze, G. Brasche, K. M. Gericke), Wiley-VCH, 2006; ISBN 3-527-29060-5.
    • (2006) Domino Reactions in Organic Synthesis
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    • For an application to the first enantioselective synthesis of iridal see
    • b) For an application to the first enantioselective synthesis of iridal see: A. Corbu, M. Aquino, T. V. Pratap, P. Retailleau, S. Arseniyadis, Org. Lett. 2008, 10, 1787-1790.
    • (2008) Org. Lett. , vol.10 , pp. 1787-1790
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    • Several protocols were examined; all conditions failed in our hands
    • W. Lehnert, Tetrahedron 1973, 29, 635-638. Several protocols were examined; all conditions failed in our hands.
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    • [8] (Figure Presented)
    • [8] (Figure Presented)
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    • -1), with the C-3 methyl ester showing better potency than, its corresponding free (galbanic) acid
    • -1), with the C-3 methyl ester showing better potency than, its corresponding free (galbanic) acid: C. L. Lee, L. C. Chiang, L. H. Cheng, C. C. Liaw, M. H. Abd El-Razek, F. R. Chang, Y. C. Wu, J. Nat. Prod. 2009, 72, 1568-1572.
    • (2009) J. Nat. Prod. , vol.72 , pp. 1568-1572
    • Lee, C.L.1    Chiang, L.C.2    Cheng, L.H.3    Liaw, C.C.4    Abd El-Razek, M.H.5    Chang, F.R.6    Wu, Y.C.7
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.