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Volumn 1, Issue 11, 1999, Pages 1851-1854

Intramolecular addition of stabilized enolates to (η6-arene)ruthenium complexes: Synthesis of Ru-coordinated azaspirocycles

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EID: 0000068002     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol991123v     Document Type: Article
Times cited : (17)

References (31)
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  • 2
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    • Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Elsevier Science Ltd.: Oxford
    • (b) Davies, S. G.; McCarthy, T. D. In Comprehensive Organometallic Chemistry II; Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Elsevier Science Ltd.: Oxford, 1995; Vol. 12, pp 1039-1070.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 1039-1070
    • Davies, S.G.1    McCarthy, T.D.2
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    • Trost, B. M., Fleming, L. Eds.; Pergamon: Oxford
    • (a) Semmelhack, M. F. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, L. Eds.; Pergamon: Oxford, 1991; Vol. 4, pp 517-549.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 517-549
    • Semmelhack, M.F.1
  • 5
    • 0000958965 scopus 로고
    • Liebeskind, L. S., Ed.; Jai Press Ltd.: Greenwich, CT
    • (b) Uemura, M. In Advances in Metal-Organic Chemistry; Liebeskind, L. S., Ed.; Jai Press Ltd.: Greenwich, CT, 1991; Vol. 2, pp 195-245.
    • (1991) Advances in Metal-organic Chemistry , vol.2 , pp. 195-245
    • Uemura, M.1
  • 14
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    • 13C-NMR, and IR) and analytical (combustion analysis) data consistent with the assigned structures
    • 13C-NMR, and IR) and analytical (combustion analysis) data consistent with the assigned structures.
  • 20
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    • All crystallographic data will be deposited in the Cambridge Structural Database
    • All crystallographic data will be deposited in the Cambridge Structural Database.
  • 25
    • 0001694806 scopus 로고
    • Semmelhack, M. F.; Yamashita, A. J. Am. Chem. Soc. 1980, 102, 5924. See also: Chamberlin, S.; Wulff, W. D. J. Am. Chem. Soc. 1992, 114, 10667.
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    • Chamberlin, S.1    Wulff, W.D.2
  • 26
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    • Complexes 9 and 10 were prepared from the corresponding benzylamines using a route analogous to that shown in Scheme 2
    • Complexes 9 and 10 were prepared from the corresponding benzylamines using a route analogous to that shown in Scheme 2.
  • 27
    • 0007856289 scopus 로고
    • and references therein
    • For a discussion of regioselectivity in nucleophilic additions to substituted (arene)metal complexes, see: Sutherland, R. G.; Zhang, C.; Piórko, A. J. Organamet. Chem. 1991, 419, 357 and references therein.
    • (1991) J. Organamet. Chem. , vol.419 , pp. 357
    • Sutherland, R.G.1    Zhang, C.2    Piórko, A.3
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    • Walser-Volken, P.; Tamm, Ch. In Progress in the Chemistry of Organic Natural Products; Herz, W., Kirby, G. W., Moore, R. E., Steglich, W., Tamm, Ch., Eds.; Springer: New York, 1996; Vol. 67, pp 125-165.
    • (1996) Progress in the Chemistry of Organic Natural Products , vol.67 , pp. 125-165
    • Walser-Volken, P.1    Tamm, Ch.2
  • 30
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    • Daly, J. W.; Garraffo, H. M.; Spande, T. F. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: New York, 1993; Vol. 43, pp 186-288.
    • (1993) The Alkaloids , vol.43 , pp. 186-288
    • Daly, J.W.1    Garraffo, H.M.2    Spande, T.F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.