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Volumn 54, Issue 14, 1998, Pages 3457-3464

On the oxazaborolidine-catalyzed borane reduction of 1-tetralone-Cr(CO)3 complexes: The control of the reagent over a strong substrate

Author keywords

[No Author keywords available]

Indexed keywords

CHROMIUM DERIVATIVE;

EID: 0032473893     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)00078-7     Document Type: Article
Times cited : (24)

References (39)
  • 1
    • 0010617428 scopus 로고
    • (Eds.: Werner, H.; Erker, G.), Springer-Verlag: Berlin Heidelberg
    • 1. a) Schlögl, K. in Organometallics in Organic Synthesis 2 (Eds.: Werner, H.; Erker, G.), Springer-Verlag: Berlin Heidelberg, 1989, p. 63 and cited ref.;
    • (1989) Organometallics in Organic Synthesis , vol.2 , pp. 63
    • Schlögl, K.1
  • 2
    • 0002933593 scopus 로고
    • Liebeskind, L.S. (Ed.), JAI Press: London, and refs. cited therein
    • b) Solladié-Cavallo, A. in Advances in Metal Organic Chemistry, Vol. 2 ; Liebeskind, L.S. (Ed.), JAI Press: London, 1989, p. 99; and refs. cited therein.
    • (1989) Advances in Metal Organic Chemistry , vol.2 , pp. 99
    • Solladié-Cavallo, A.1
  • 3
    • 0000958965 scopus 로고
    • Liebeskind, L.S. (Ed.), JAI Press: London
    • 2. See, for instance: a) Uemura, M. in Advances in Metal Organic Chemistry, Vol. 2; Liebeskind, L.S. (Ed.), JAI Press: London, 1989, p. 195; for recent work from this laboratory, see:
    • (1989) Advances in Metal Organic Chemistry , vol.2 , pp. 195
    • Uemura, M.1
  • 10
    • 0000747080 scopus 로고
    • Abel, E.W.; Stone, F.G.A.; Wilkinson, G. (Eds.); Pergamon: Oxford
    • b) Semmelhack, M.F. in Comprehensive Organometallic Chemistry II, Vol. 12, Abel, E.W.; Stone, F.G.A.; Wilkinson, G. (Eds.); Pergamon: Oxford, 1995, p. 979;
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 979
    • Semmelhack, M.F.1
  • 24
    • 33748638673 scopus 로고
    • 9. a) Schmalz, H.-G.; Millies, B.; Bats, J.W.; Dürner, G. Angew. Chem. 1992, 104, 640; Angew. Chem. Int. Ed. Engl. 1992, 31, 631;
    • (1992) Angew. Chem. Int. Ed. Engl. , vol.31 , pp. 631
  • 32
    • 0010617047 scopus 로고    scopus 로고
    • note
    • 12. The depicted structures (specified by bold arabic numbers) represent also the absolute configuration of the corresponding molecules. An enantiomeric structure is specified by adding the prefix ent-to the bold arabic number.
  • 34
    • 84985530075 scopus 로고
    • 13. Masamune, S.; Choy, W.; Pedersen, J.S.; Sita, L.R. Angew. Chem. 1985, 97, 1; Angew. Chem. Int. Ed. Engl. 1985, 24, 1.
    • (1985) Angew. Chem. Int. Ed. Engl. , vol.24 , pp. 1
  • 35
    • 0010614581 scopus 로고    scopus 로고
    • note
    • 9a,18.
  • 36
    • 0003942864 scopus 로고
    • Wiley, New York
    • 15. For the dependency of the enantiomeric excess on the conversion in kinetic resolutions, see, for example: Eliel, E.L.; Wilen, S.H. Stereochemistry of Organic Compounds, Wiley, New York 1994, pp. 395.
    • (1994) Stereochemistry of Organic Compounds , pp. 395
    • Eliel, E.L.1    Wilen, S.H.2
  • 37
    • 0010548107 scopus 로고    scopus 로고
    • note
    • 3 in the presence of 0.3 eq 3a (73% conversion). In this case, the re-isolated ketone complex (4a) had an enantiomeric purity of 98% e.e..


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