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Volumn , Issue 9, 2011, Pages 1682-1694

Synthetic studies towards pectenotoxin-2: Synthesis of the nonanomeric 10-epi-ABCDE ring segment by kinetic spiroketalization

Author keywords

Anomeric effect; Chirality; Enantioselectivity; Natural products; Spiro compounds

Indexed keywords


EID: 79952515587     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201001411     Document Type: Article
Times cited : (19)

References (63)
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    • For key references on the isolation and characterization of PTX congeners, see
    • For key references on the isolation and characterization of PTX congeners, see
  • 10
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    • For a review of PTXs, see
    • For a review of PTXs, see
  • 13
    • 79952501056 scopus 로고    scopus 로고
    • For references to the seco acids PTX2sa and 7-epi-PTX2sa, see
    • For references to the seco acids PTX2sa and 7-epi-PTX2sa, see
  • 18
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    • For selected examples, see
    • For selected examples, see
  • 26
    • 79952497137 scopus 로고    scopus 로고
    • For leading references to other synthetic approaches to PTXs, see
    • For leading references to other synthetic approaches to PTXs, see
  • 30
    • 85047698843 scopus 로고    scopus 로고
    • total synthesis of the anomeric congener, PTX4
    • Angew. Chem. Int. Ed. 2002, 41, 4573 (total synthesis of the anomeric congener, PTX4)
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 4573
  • 43
    • 33847767608 scopus 로고    scopus 로고
    • For an excellent example of an alternative synthesis of the nonanomeric spiroketal system of PTX2, see:,. for a review of nonanomeric spiroketals, see:, Chem. Rev. 2005, 105, 4406.
    • For an excellent example of an alternative synthesis of the nonanomeric spiroketal system of PTX2, see:, D. Vellucci, S. D. Rychnovsky, Org. Lett. 2007, 9, 711. for a review of nonanomeric spiroketals, see:, J. E. Aho, P. M. Pihko, T. K. Rissa, Chem. Rev. 2005, 105, 4406.
    • (2007) Org. Lett. , vol.9 , pp. 711
    • Vellucci, D.1    Rychnovsky, S.D.2    Aho, J.E.3    Pihko, P.M.4    Rissa, T.K.5
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    • 33746333004 scopus 로고    scopus 로고
    • For an excellent discussion, see and references therein
    • For an excellent discussion, see: D. A. Evans, V. J. Cee, S. J. Siska, J. Am. Chem. Soc. 2006, 128, 9433 and references therein.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 9433
    • Evans, D.A.1    Cee, V.J.2    Siska, S.J.3
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    • For an account of the development of metathesis catalysts, see.
    • For an account of the development of metathesis catalysts, see:, T. M. Trnka, R. H. Grubbs, Acc. Chem. Res. 2001, 34, 18.
    • (2001) Acc. Chem. Res. , vol.34 , pp. 18
    • Trnka, T.M.1    Grubbs, R.H.2
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    • 22744453115 scopus 로고    scopus 로고
    • for a review on metathesis reactions in total synthesis, see:,; Angew. Chem. Int. Ed. 2005, 44, 4490.
    • for a review on metathesis reactions in total synthesis, see:, K. C. Nicolaou, P. G. Bulger, D. Sarlah, Angew. Chem. 2005, 117, 4564; Angew. Chem. Int. Ed. 2005, 44, 4490.
    • (2005) Angew. Chem. , vol.117 , pp. 4564
    • Nicolaou, K.C.1    Bulger, P.G.2    Sarlah, D.3
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    • See the Supporting Information for details.
    • See the Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.