메뉴 건너뛰기




Volumn 107, Issue 1-3, 1996, Pages 85-94

Enantioselective hydrogenation of α-ketoesters: Comparison of homogeneous and heterogeneous catalysts

Author keywords

(R) Hydroxyesters; Cinchona modified catalysts; Enantioselectivity; Hydrogenation; Platinum; Process development; Rhodium diphosphine complexes; Solvent effects; Ketoesters

Indexed keywords

ALUMINA; CATALYST SELECTIVITY; COMPOSITION EFFECTS; ESTERS; HYDROGENATION; PLATINUM; SUBSTRATES;

EID: 0030572042     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/1381-1169(95)00164-6     Document Type: Article
Times cited : (70)

References (32)
  • 1
  • 3
    • 0001217240 scopus 로고    scopus 로고
    • EP 0 206 993 Al, assigned to Ciba-Geigy (1986)
    • H.U. Blaser, H.P. Jalett and G.H. Sedelmeier, EP 0 206 993 Al, assigned to Ciba-Geigy (1986). H. Yanagisawa, S. Ishihara, A. Ando, T. Kanazaki, S. Miyamoto, H. Koike, Y. Iijima, K. Oizumi, Y. Matsushita and T. Hata, J. Med. Chem., 31 (1988) 422.
    • Blaser, H.U.1    Jalett, H.P.2    Sedelmeier, G.H.3
  • 5
    • 0038653828 scopus 로고
    • Merck & Co., Inc., Rahway, NJ
    • S. Budavari (Ed.), The Merck Index, 11th Edition, Merck & Co., Inc., Rahway, NJ, 1989, p. 2465 and 6961-6964, and references cited therein.
    • (1989) The Merck Index, 11th Edition , pp. 2465
    • Budavari, S.1
  • 15
    • 24044538252 scopus 로고    scopus 로고
    • note
    • Later we learned that E. Broger (Hoffmann-La Roche) had developed a Ru-biphemp catalyst for the enantioselective hydrogenation of (1) with even slightly better ee of 97%. E. Broger, Plenary lecture, Europacat-I, Montpellier, Sept. 1993.
  • 17
    • 85008585578 scopus 로고
    • Y. Orito, S. Imai, S. Niwa and Nguyen G.-H, J. Synth. Org. Chem. Jpn. 37 (1979) 173. Y. Orito, S. Imai and S. Niwa, J. Chem. Soc. Jpn. (1979) 1118., (1980) 670 and (1982) 137.
    • (1979) J. Chem. Soc. Jpn. , pp. 1118
    • Orito, Y.1    Imai, S.2    Niwa, S.3
  • 18
    • 84906377691 scopus 로고
    • Y. Orito, S. Imai, S. Niwa and Nguyen G.-H, J. Synth. Org. Chem. Jpn. 37 (1979) 173. Y. Orito, S. Imai and S. Niwa, J. Chem. Soc. Jpn. (1979) 1118., (1980) 670 and (1982) 137.
    • (1980) J. Chem. Soc. Jpn. , pp. 670
  • 19
    • 84906377691 scopus 로고
    • Y. Orito, S. Imai, S. Niwa and Nguyen G.-H, J. Synth. Org. Chem. Jpn. 37 (1979) 173. Y. Orito, S. Imai and S. Niwa, J. Chem. Soc. Jpn. (1979) 1118., (1980) 670 and (1982) 137.
    • (1982) J. Chem. Soc. Jpn. , pp. 137
  • 27
    • 37049089621 scopus 로고
    • Some recent papers confirm that cinchona alkaloids are still the best modifiers. S.P. Griffiths, P. Johnston, W.A.H. Vermeer and P.B. Wells, J. Chem. Soc., Chem. Commun., (1994) 2431. A. Tungler, T. Tarnai, T. Mathe, J. Petro and R.A. Sheldon, in G. Jannes and V. Dubois (Eds.), Chiral Reactions in Heterogeneous Catalysis, Plenum Press, New York, 1995, p. 33.
    • (1994) J. Chem. Soc., Chem. Commun. , pp. 2431
    • Griffiths, S.P.1    Johnston, P.2    Vermeer, W.A.H.3    Wells, P.B.4
  • 28
    • 0002148577 scopus 로고
    • G. Jannes and V. Dubois (Eds.), Plenum Press, New York
    • Some recent papers confirm that cinchona alkaloids are still the best modifiers. S.P. Griffiths, P. Johnston, W.A.H. Vermeer and P.B. Wells, J. Chem. Soc., Chem. Commun., (1994) 2431. A. Tungler, T. Tarnai, T. Mathe, J. Petro and R.A. Sheldon, in G. Jannes and V. Dubois (Eds.), Chiral Reactions in Heterogeneous Catalysis, Plenum Press, New York, 1995, p. 33.
    • (1995) Chiral Reactions in Heterogeneous Catalysis , pp. 33
    • Tungler, A.1    Tarnai, T.2    Mathe, T.3    Petro, J.4    Sheldon, R.A.5
  • 30
    • 0001054290 scopus 로고
    • Recently some simpler amines were shown to be moderately selective. G. Wang, T. Heinz, A. Pfaltz, B. Minder, T. Mallat and A. Baiker, J. Chem. Soc., Chem. Commun., (1994) 2047. B. Minder, M. Schürch, T. Mallat and A. Baiker, Catal. Lett., 31 (1995) 143.
    • (1995) Catal. Lett. , vol.31 , pp. 143
    • Minder, B.1    Schürch, M.2    Mallat, T.3    Baiker, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.