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Volumn 46, Issue 40, 2007, Pages 7651-7654

Highly diastereoselective formation of ruthenium complexes for efficient catalytic asymmetric transfer hydrogenation

Author keywords

Asymmetric catalysis; Chiral resolution; Hydrogen transfer; Phosphane ligands; Ruthenium

Indexed keywords

CATALYSIS; CATALYST ACTIVITY; HYDROGENATION; LIGANDS; METAL COMPLEXES; STEREOSELECTIVITY;

EID: 35048842033     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200702278     Document Type: Article
Times cited : (107)

References (40)
  • 1
    • 84890985460 scopus 로고    scopus 로고
    • Eds, J. G. de Vries, C. J. Elsevier, Wiley-VCH, Weinheim
    • a) The Handbook of Homogeneous Hydrogenation, Vol. 1-3 (Eds.: J. G. de Vries, C. J. Elsevier), Wiley-VCH, Weinheim, 2007;
    • (2007) The Handbook of Homogeneous Hydrogenation , vol.1-3
  • 2
    • 0034697497 scopus 로고    scopus 로고
    • Eds, H. U. Blaser, E. Schmidt, Wiley-VCH, Weinheim
    • b) Asymmetric Catalysis on Industrial Scale (Eds.: H. U. Blaser, E. Schmidt), Wiley-VCH, Weinheim, 2004;
    • (2004) Asymmetric Catalysis on Industrial Scale
  • 3
    • 35048830529 scopus 로고    scopus 로고
    • Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Berlin
    • c) Comprehensive Asymmetric Catalysis, Supplements 1-2 (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, 2004;
    • (2004) Comprehensive Asymmetric Catalysis, Supplements , pp. 1-2
  • 4
    • 0003544583 scopus 로고    scopus 로고
    • 2nd ed, Ed, I. Ojima, Wiley-VCH, New York
    • d) Catalytic Asymmetric Synthesis, 2nd ed. (Ed.: I. Ojima), Wiley-VCH, New York, 2000.
    • (2000) Catalytic Asymmetric Synthesis
  • 6
  • 20
  • 29
  • 30
    • 23044487624 scopus 로고    scopus 로고
    • For a review on the stereoselective synthesis of optically active 1-substituted-1-(pyridin-2-yl)methanamines, see: a
    • For a review on the stereoselective synthesis of optically active 1-substituted-1-(pyridin-2-yl)methanamines, see: a) G. Chelucci, Tetrahedron: Asymmetry 2005, 16, 2353.
    • (2005) Tetrahedron: Asymmetry , vol.16 , pp. 2353
    • Chelucci, G.1
  • 33
    • 35048893464 scopus 로고    scopus 로고
    • /Josiphos/Pyme = 1:1.5:1; acetophenone/Ru/NaOiPr = 2000:1:40; TOF at 50% conversion.
    • [Ru]/Josiphos/Pyme = 1:1.5:1; acetophenone/Ru/NaOiPr = 2000:1:40; TOF at 50% conversion.
  • 34
    • 35048842912 scopus 로고    scopus 로고
    • NMR spectroscopic data for 1-5 and the X-ray crystal analysis of 1 and 2 are provided as Supporting Information.
    • NMR spectroscopic data for 1-5 and the X-ray crystal analysis of 1 and 2 are provided as Supporting Information.
  • 35
    • 35048823040 scopus 로고    scopus 로고
    • 31P{1H} NMR spectrum in toluene with CD 2Cl2 (10% in as internal lock: δ, 61.6 (d, 2J(P,P, 40.9 Hz) and 41.1 ppm (d, 2J(P,P, 40.9 Hz, compound 1, major product, δ, 59.2 (d, 2J(P,P, 38.6 Hz) and 39.2 ppm (d, 2J(P,P, 38.6 Hz, δ, 58.8 (d, 2J(P,P, 39.3 Hz) and 47.4 ppm (d, 2JP,P, 39.3 Hz, minor product
    • (P,P) = 39.3 Hz), minor product.
  • 36
    • 35048877768 scopus 로고    scopus 로고
    • (PP) = 38.5 Hz).
    • (PP) = 38.5 Hz).
  • 40
    • 25844443346 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 6214.
    • (2005) Chem. Int. Ed , vol.44 , pp. 6214
    • Angew1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.