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Volumn 56, Issue 18, 2000, Pages 2789-2798

Phosphine effects in the copper(I) hydride-catalyzed hydrogenation of ketones and regioselective 1,2-reduction of α,β-unsaturated ketones and aldehydes. Hydrogenation of decalin and steroidal ketones and enones

Author keywords

Carbonyl compounds; Catalysis; Copper and compounds; Hydrogenation

Indexed keywords

ALDEHYDE; DECALIN; KETONE DERIVATIVE; PHOSPHINE;

EID: 0034724764     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(00)00133-2     Document Type: Article
Times cited : (103)

References (44)
  • 1
    • 0039004514 scopus 로고
    • (a) Scaros, M. G., Prunier, M. L., Eds.; Marcel Dekker: New York
    • (a) Daeuble, J. F., Stryker, J. M. Catalysis of Organic Reactions; Scaros, M. G., Prunier, M. L., Eds.; Marcel Dekker: New York, 1995; pp 235-247 (Chem. Ind. 1995, 62).
    • (1995) Catalysis of Organic Reactions; , pp. 235-247
    • Daeuble, J.F.1    Stryker, J.M.2
  • 2
    • 84992246351 scopus 로고
    • (a) Daeuble, J. F., Stryker, J. M. Catalysis of Organic Reactions; Scaros, M. G., Prunier, M. L., Eds.; Marcel Dekker: New York, 1995; pp 235-247 (Chem. Ind. 1995, 62).
    • (1995) Chem. Ind. , pp. 62
  • 4
    • 0000239724 scopus 로고
    • The ruthenium hydrogenation catalyst reported by Noyori et al., is also selective for the 1,2-reduction of unsaturated carbonyl compounds, including asymmetric hydrogenation
    • The ruthenium hydrogenation catalyst reported by Noyori et al., is also selective for the 1,2-reduction of unsaturated carbonyl compounds, including asymmetric hydrogenation: Ohkuma, T.; Ooka, H.; Ikariya, T.; Noyori, R. J. Am. Chem. Soc. 1995, 117, 10417.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 10417
    • Ohkuma, T.1    Ooka, H.2    Ikariya, T.3    Noyori, R.4
  • 5
    • 84992276204 scopus 로고    scopus 로고
    • For references to other catalysts for the chemoselective hydrogenation and hydrosilylation of unsaturated carbonyl compounds, see the citations provided in Ref. 1b
    • For references to other catalysts for the chemoselective hydrogenation and hydrosilylation of unsaturated carbonyl compounds, see the citations provided in Ref. 1b.
  • 8
    • 84992236957 scopus 로고
    • (b) Stryker, J. M., Mahoney, W. S., Daeuble, J. F., Brestensky, D. M. Catalysis of Organic Reactions; W. E. Pascoe, Ed.; Marcel Dekker: New York, 1992; pp 29-44 (Chem. Ind. 1992, 47).
    • (1992) Chem. Ind. , pp. 47
  • 14
    • 84992254101 scopus 로고    scopus 로고
    • For discussion of phosphine ligand effects, see Ref. 1b. Catalysts derived from a range of monodentate and polydentate nitrogen ligand systems, as well as carbene ligands of the 1,3-imidazolin-2-ylidene class, have also been screened without success
    • For discussion of phosphine ligand effects, see Ref. 1b. Catalysts derived from a range of monodentate and polydentate nitrogen ligand systems, as well as carbene ligands of the 1,3-imidazolin-2-ylidene class, have also been screened without success.
  • 17
    • 0001324442 scopus 로고
    • (c) To avoid the variable quality of material provided by some commercial producers, the complex is best prepared rather than purchased. Benchtop, One-Pot Preparation
    • (c) To avoid the variable quality of material provided by some commercial producers, the complex is best prepared rather than purchased. Benchtop, One-Pot Preparation: Brestensky, D. M.; Huseland, D. E.; McGettigan, C.; Stryker, J. M. Tetrahedron Lett. 1988, 29, 3749.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 3749
    • Brestensky, D.M.1    Huseland, D.E.2    McGettigan, C.3    Stryker, J.M.4
  • 18
    • 84992284387 scopus 로고    scopus 로고
    • 1a
    • 1a.
  • 19
    • 84992267804 scopus 로고
    • Ph.D. dissertation, Indiana University
    • Daeuble, J. F. Ph.D. dissertation, Indiana University, 1993.
    • (1993)
    • Daeuble, J.F.1
  • 21
    • 84992254170 scopus 로고    scopus 로고
    • 4; see, for example
    • 4; see, for example
  • 23
  • 25
    • 84992246346 scopus 로고    scopus 로고
    • 1H NMR spectrum of this methine resonance (δ 5.05, br s)
    • 1H NMR spectrum of this methine resonance (δ 5.05, br s).
  • 26
    • 84992272033 scopus 로고    scopus 로고
    • 1b
    • 1b.
  • 31
    • 84982334816 scopus 로고
    • Steiger, M.; Reichstein, T. Helv. Chim. Acta 1938, 21, 546; NMR spectroscopy: Bridgeman, J. E.; Cherry, P. C.; Clegg, A. S.; Evans, J. M.; Jones, R. H.; Kasal, A.; Kumar, V.; Meakins, G. D.; Morisawa, Y.; Richards, E. E.; Woodgate, P. D. J. Chem. Soc. (C) 1970, 250.
    • (1938) Helv. Chim. Acta , vol.21 , pp. 546
    • Steiger, M.1    Reichstein, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.