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Volumn 133, Issue 15, 2011, Pages 5776-5779

Ethylene in organic synthesis. repetitive hydrovinylation of alkenes for highly enantioselective syntheses of pseudopterosins

Author keywords

[No Author keywords available]

Indexed keywords

CHIRAL CENTERS; CHIRAL INTERMEDIATES; DIASTEREO-SELECTIVITY; DIASTEREOMERIC; ENANTIOSELECTIVE SYNTHESIS; EXISTING METHOD; HYDROVINYLATION; NATURAL PRODUCTS; ORGANIC SYNTHESIS; PSEUDOPTEROSINS; VINYL GROUP;

EID: 79954490071     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja201321v     Document Type: Article
Times cited : (53)

References (51)
  • 1
    • 0000554241 scopus 로고    scopus 로고
    • Hydrovinylation
    • For examples of the use of unactivated alkenes including ethylene as reagents in catalytic reactions, see:; In;, Eds.; VCH: New York,; Vol., pp - 1048.
    • For examples of the use of unactivated alkenes including ethylene as reagents in catalytic reactions, see: Jolly, P. W.; Wilke, G. Hydrovinylation In Applied Homogeneous Catalysis with Organometallic Compounds; Cornils, B., Herrmann, W. A., Eds.; VCH: New York, 1996; Vol. 2, pp 1024 - 1048.
    • (1996) Applied Homogeneous Catalysis with Organometallic Compounds , vol.2 , pp. 1024
    • Jolly, P.W.1    Wilke, G.2    Cornils, B.3    Herrmann, W.A.4
  • 5
    • 58149340327 scopus 로고    scopus 로고
    • For recent, representative examples of use of ethylene in fine chemical synthesis:;;;; J. Am. Chem. Soc. 2003, 5606
    • Hess, W.; Treutwein, J.; Hilt, G. Synthesis 2008, 3537 For recent, representative examples of use of ethylene in fine chemical synthesis: Mori, M.; Saito, N.; Tanaka, D.; Takimoto, M.; Sato, Y. J. Am. Chem. Soc. 2003, 125, 5606
    • (2008) Synthesis , vol.125 , pp. 3537
    • Hess, W.1    Treutwein, J.2    Hilt, G.3    Mori, M.4    Saito, N.5    Tanaka, D.6    Takimoto, M.7    Sato, Y.8
  • 10
    • 78149250621 scopus 로고    scopus 로고
    • For an outstanding example of iterative use of an asymmetric C-C bond-forming reaction in natural product synthesis, see
    • For an outstanding example of iterative use of an asymmetric C-C bond-forming reaction in natural product synthesis, see: Han, S. B.; Hassan, A.; Kim, I. S.; Krische, M. J. J. Am. Chem. Soc. 2010, 132, 15559
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 15559
    • Han, S.B.1    Hassan, A.2    Kim, I.S.3    Krische, M.J.4
  • 11
    • 1842862775 scopus 로고    scopus 로고
    • For a review of asymmetric catalysis in complex molecule synthesis, see
    • For a review of asymmetric catalysis in complex molecule synthesis, see: Taylor, M. S.; Jacobsen, E. N. Proc. Natl. Acad. Sci. U. S. A. 2004, 101, 5368
    • (2004) Proc. Natl. Acad. Sci. U. S. A. , vol.101 , pp. 5368
    • Taylor, M.S.1    Jacobsen, E.N.2
  • 14
    • 79954456290 scopus 로고    scopus 로고
    • See also ref 9.
    • See also ref 9.
  • 29
    • 79954473772 scopus 로고    scopus 로고
    • Details of the experimental procedures, and spectroscopic and chromatographic data for all compounds are included in the Supporting Information.
    • Details of the experimental procedures, and spectroscopic and chromatographic data for all compounds are included in the Supporting Information.
  • 31
    • 44449114350 scopus 로고    scopus 로고
    • For phosphoramidites as ligands for asymmetric hydrovinylation of vinylarenes, see:;; J. Am. Chem. Soc. 2002, 124, 736
    • Smith, C. R.; RajanBabu, T. V. Org. Lett. 2008, 10, 1657 For phosphoramidites as ligands for asymmetric hydrovinylation of vinylarenes, see: Francio, G.; Faraone, F.; Leitner, W. J. Am. Chem. Soc. 2002, 124, 736
    • (2008) Org. Lett. , vol.10 , pp. 1657
    • Smith, C.R.1    Rajanbabu, T.V.2    Francio, G.3    Faraone, F.4    Leitner, W.5
  • 32
    • 4544228993 scopus 로고    scopus 로고
    • For hydroboration/oxidation of hydrovinylation products, see
    • For hydroboration/oxidation of hydrovinylation products, see: Zhang, A.; RajanBabu, T. V. Org. Lett. 2004, 6, 3159
    • (2004) Org. Lett. , vol.6 , pp. 3159
    • Zhang, A.1    Rajanbabu, T.V.2
  • 38
    • 79954549887 scopus 로고    scopus 로고
    • 3 reduction of the resulting 1,3-diene. See Supporting Information for details.
    • 3 reduction of the resulting 1,3-diene. See Supporting Information for details.
  • 49
    • 4744368087 scopus 로고    scopus 로고
    • The conclusions of this paper has since been questioned
    • The conclusions of this paper has since been questioned: Zanoni, G.; Franzini, M. Angew. Chem., Int. Ed. 2004, 43, 4837
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 4837
    • Zanoni, G.1    Franzini, M.2
  • 50
    • 0142183446 scopus 로고    scopus 로고
    • For a synthesis of elisapterosin B and of ent -2- epi -elisabethin A, see:;;, See also refs 21b-21e for other syntheses of elisapterosin B.
    • For a synthesis of elisapterosin B and of ent -2- epi -elisabethin A, see: Waizumi, N.; Stankovic, A. R.; Rawal, V. H. J. Am. Chem. Soc. 2003, 125, 13022 See also refs 21b-21e for other syntheses of elisapterosin B.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 13022
    • Waizumi, N.1    Stankovic, A.R.2    Rawal, V.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.