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Volumn 10, Issue 11, 2008, Pages 2211-2214

Stereocontrolled synthesis of the A/B-ring fragment of gambieric acid B: Reassignment of the absolute configuration of the polycyclic ether region

Author keywords

[No Author keywords available]

Indexed keywords

CIGUATOXIN; GAMBIERIC ACID B; POLYCYCLIC HYDROCARBON;

EID: 52649124890     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol800642t     Document Type: Article
Times cited : (23)

References (39)
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    • For reviews of marine polycyclic ether natural products, see: a
    • For reviews of marine polycyclic ether natural products, see: (a) Yasumoto, T.; Murata, M. Chem. Rev 1993, 93, 1897.
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    • Yasumoto, T.1    Murata, M.2
  • 5
    • 0012147007 scopus 로고    scopus 로고
    • For recent reviews of the synthesis of polycyclic ethers, see: a
    • For recent reviews of the synthesis of polycyclic ethers, see: (a) Marmsäter, F. P.; West, F. G. Chem. Eur. J. 2002, 8, 4347.
    • (2002) Chem. Eur. J , vol.8 , pp. 4347
    • Marmsäter, F.P.1    West, F.G.2
  • 7
    • 30744476469 scopus 로고    scopus 로고
    • (c) Inoue, M. Chem. Rev. 2005, 105, 4379.
    • (2005) Chem. Rev , vol.105 , pp. 4379
    • Inoue, M.1
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    • 30744459350 scopus 로고    scopus 로고
    • (d) Nakata, T. Chem. Rev. 2005, 105, 4314.
    • (2005) Chem. Rev , vol.105 , pp. 4314
    • Nakata, T.1
  • 25
    • 2042507954 scopus 로고
    • For reviews of Suzuki-Miyaura coupling, see: a
    • For reviews of Suzuki-Miyaura coupling, see: (a) Suzuki, A.; Miyaura, N. Chem. Rev. 1995, 95, 2457.
    • (1995) Chem. Rev , vol.95 , pp. 2457
    • Suzuki, A.1    Miyaura, N.2
  • 27
    • 59849109079 scopus 로고    scopus 로고
    • The numbering of carbon atoms of all compounds in this paper corresponds to that of the natural product
    • The numbering of carbon atoms of all compounds in this paper corresponds to that of the natural product.
  • 35
    • 59849120787 scopus 로고    scopus 로고
    • Our previous explanation12 for the stereochemical outcome of the bromoetherification has turned out to be misleading, since this method could also be effective for the construction of the A-ring of compounds 1b-d. For plausible rationales for the diastereoselectivity of the bromoetherifications in the synthesis of 1b-d, see Supporting Information
    • 12 for the stereochemical outcome of the bromoetherification has turned out to be misleading, since this method could also be effective for the construction of the A-ring of compounds 1b-d. For plausible rationales for the diastereoselectivity of the bromoetherifications in the synthesis of 1b-d, see Supporting Information.
  • 38
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    • 5N. See Supporting Information for details.
    • 5N. See Supporting Information for details.
  • 39
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    • See Supporting Information for details
    • See Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.