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Volumn 125, Issue 9, 2003, Pages 2591-2596

An enantiomerically pure adamantylimido molybdenum alkylidene complex. An effective new catalyst for enantioselective olefin metathesis

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS; ISOMERS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OLEFINS; SYNTHESIS (CHEMICAL); X RAY ANALYSIS;

EID: 0142046305     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja021204d     Document Type: Article
Times cited : (76)

References (36)
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    • For an overview of chiral Mo-based olefin metathesis catalysts, see: Hoveyda, A. H.; Schrock, R. R. Chem. Eur. J. 2001, 7, 945-950.
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    • For reports on chiral Ru catalysts for olefin metathesis, see: (a) Seiders, T. J.; Ward, D. W.; Grubbs, R. H. Org. Lett. 2001, 3, 3225-3228.m (b) Van Veldhuizen, J. J.; Garber, S. B.; Kingsbury, J. S.; Hoveyda, A. H. J. Am. Chem. Soc. 2002, 124, 4954-4955. For a recent report regarding chiral W-based catalysts for olefin metathesis, see: (c) Tsang, W. C. P.; Hultzsch, K. C.; Alexander, J. B.; Bonitatebus, P. J., Jr.; Schrock, R. R.; Hoveyda, A. H. J. Am. Chem. Soc. 2003, 125, in press.
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    • 0037042233 scopus 로고    scopus 로고
    • For reports on chiral Ru catalysts for olefin metathesis, see: (a) Seiders, T. J.; Ward, D. W.; Grubbs, R. H. Org. Lett. 2001, 3, 3225-3228.m (b) Van Veldhuizen, J. J.; Garber, S. B.; Kingsbury, J. S.; Hoveyda, A. H. J. Am. Chem. Soc. 2002, 124, 4954-4955. For a recent report regarding chiral W-based catalysts for olefin metathesis, see: (c) Tsang, W. C. P.; Hultzsch, K. C.; Alexander, J. B.; Bonitatebus, P. J., Jr.; Schrock, R. R.; Hoveyda, A. H. J. Am. Chem. Soc. 2003, 125, in press.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 4954-4955
    • Van Veldhuizen, J.J.1    Garber, S.B.2    Kingsbury, J.S.3    Hoveyda, A.H.4
  • 12
    • 20244362552 scopus 로고    scopus 로고
    • in press
    • For reports on chiral Ru catalysts for olefin metathesis, see: (a) Seiders, T. J.; Ward, D. W.; Grubbs, R. H. Org. Lett. 2001, 3, 3225-3228.m (b) Van Veldhuizen, J. J.; Garber, S. B.; Kingsbury, J. S.; Hoveyda, A. H. J. Am. Chem. Soc. 2002, 124, 4954-4955. For a recent report regarding chiral W-based catalysts for olefin metathesis, see: (c) Tsang, W. C. P.; Hultzsch, K. C.; Alexander, J. B.; Bonitatebus, P. J., Jr.; Schrock, R. R.; Hoveyda, A. H. J. Am. Chem. Soc. 2003, 125, in press.
    • (2003) J. Am. Chem. Soc. , pp. 125
    • Tsang, W.C.P.1    Hultzsch, K.C.2    Alexander, J.B.3    Bonitatebus P.J., Jr.4    Schrock, R.R.5    Hoveyda, A.H.6
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    • Refs 1a,c
    • (a) Refs 1a,c.
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    • For representative examples, where structurally related substrates require different optimum chiral catalysts, see: (a) Shimizu, K. D.; Cole, B. M.; Krueger, C. A.; Kuntz, K. W.; Snapper, M. L.; Hoveyda, A. H. Angew. Chem., Int. Ed. Engl. 1997, 36, 1704-1707. b) Ref 1b. (c) Mizutani, H.; Degrado, S. J.; Hoveyda, A. H. J. Am. Chem. Soc. 2002, 124, 779-781. For a detailed discussion regarding catalyst diversity versus specificity, see: Hoveyda, A. H. In Handbook of Combinatorial Chemistry; Nicolaou, K. C., Hanko, R., Hartwig, W., Eds.; Wiley-VCH: Weinheim. 2002; pp 991-1016.
    • (1997) Angew. Chem., Int. Ed. Engl. , vol.36 , pp. 1704-1707
    • Shimizu, K.D.1    Cole, B.M.2    Krueger, C.A.3    Kuntz, K.W.4    Snapper, M.L.5    Hoveyda, A.H.6
  • 24
    • 20244382018 scopus 로고    scopus 로고
    • Ref 1b
    • For representative examples, where structurally related substrates require different optimum chiral catalysts, see: (a) Shimizu, K. D.; Cole, B. M.; Krueger, C. A.; Kuntz, K. W.; Snapper, M. L.; Hoveyda, A. H. Angew. Chem., Int. Ed. Engl. 1997, 36, 1704-1707. b) Ref 1b. (c) Mizutani, H.; Degrado, S. J.; Hoveyda, A. H. J. Am. Chem. Soc. 2002, 124, 779-781. For a detailed discussion regarding catalyst diversity versus specificity, see: Hoveyda, A. H. In Handbook of Combinatorial Chemistry; Nicolaou, K. C., Hanko, R., Hartwig, W., Eds.; Wiley-VCH: Weinheim. 2002; pp 991-1016.
  • 25
    • 0037028561 scopus 로고    scopus 로고
    • For representative examples, where structurally related substrates require different optimum chiral catalysts, see: (a) Shimizu, K. D.; Cole, B. M.; Krueger, C. A.; Kuntz, K. W.; Snapper, M. L.; Hoveyda, A. H. Angew. Chem., Int. Ed. Engl. 1997, 36, 1704-1707. b) Ref 1b. (c) Mizutani, H.; Degrado, S. J.; Hoveyda, A. H. J. Am. Chem. Soc. 2002, 124, 779-781. For a detailed discussion regarding catalyst diversity versus specificity, see: Hoveyda, A. H. In Handbook of Combinatorial Chemistry; Nicolaou, K. C., Hanko, R., Hartwig, W., Eds.; Wiley-VCH: Weinheim. 2002; pp 991-1016.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 779-781
    • Mizutani, H.1    Degrado, S.J.2    Hoveyda, A.H.3
  • 26
    • 0001567886 scopus 로고    scopus 로고
    • Nicolaou, K. C., Hanko, R., Hartwig, W., Eds.; Wiley-VCH: Weinheim
    • For representative examples, where structurally related substrates require different optimum chiral catalysts, see: (a) Shimizu, K. D.; Cole, B. M.; Krueger, C. A.; Kuntz, K. W.; Snapper, M. L.; Hoveyda, A. H. Angew. Chem., Int. Ed. Engl. 1997, 36, 1704-1707. b) Ref 1b. (c) Mizutani, H.; Degrado, S. J.; Hoveyda, A. H. J. Am. Chem. Soc. 2002, 124, 779-781. For a detailed discussion regarding catalyst diversity versus specificity, see: Hoveyda, A. H. In Handbook of Combinatorial Chemistry; Nicolaou, K. C., Hanko, R., Hartwig, W., Eds.; Wiley-VCH: Weinheim. 2002; pp 991-1016.
    • (2002) Handbook of Combinatorial Chemistry , pp. 991-1016
    • Hoveyda, A.H.1
  • 31
    • 20244375597 scopus 로고    scopus 로고
    • note
    • For simplicity we will use the rac or S label for the entire complex, although the label refers only to the biphenolate ligand in the complex.
  • 32
    • 20244382454 scopus 로고    scopus 로고
    • note
    • See the Supporting Information for crystal data and structure refinement parameters.
  • 33
    • 20244365689 scopus 로고    scopus 로고
    • note
    • CH determination.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.