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Volumn 16, Issue 9, 2003, Pages 554-559

Nucleophilic Activation of Enones via Homogeneous Catalytic Hydrogenation: Catalytic Reductive C-C Bond Formation Under Hydrogenation Conditions

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; ENOLASE;

EID: 0242551192     PISSN: 14319268     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (10)

References (50)
  • 1
    • 0000944975 scopus 로고
    • For use of alkenes as nucleophilic partners in catalytic reductive couplings, see: (a) Kablaoui, N.M., Buchwald, S.L. J. Am. Chem. Soc. 1995, 117, 6785;
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 6785
    • Kablaoui, N.M.1    Buchwald, S.L.2
  • 4
    • 0033618102 scopus 로고    scopus 로고
    • For use of alkynes as nucleophilic partners in catalytic reductive couplings, see: (a) Tang, X.Q., Montgomery, J. J. Am. Chem. Soc. 1999, 121, 6098;
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6098
    • Tang, X.Q.1    Montgomery, J.2
  • 7
    • 0000191874 scopus 로고
    • For use of enones as nucleophilic partners in catalytic reductive couplings, see: (a) Revis, A., Hilty, T.K. Tetrahedron Lett. 1987, 28, 4809;
    • (1987) Tetrahedron Lett. , vol.28 , pp. 4809
    • Revis, A.1    Hilty, T.K.2
  • 25
    • 0026418434 scopus 로고
    • For reviews, see: (a) Trost, B.M. Science 1991, 254, 1471;
    • (1991) Science , vol.254 , pp. 1471
    • Trost, B.M.1
  • 27
    • 0000563579 scopus 로고
    • Trost, B.M., ed, Permagon: New York
    • For selected reviews on the conjugate reduction of enones via catalytic hydrogenation, see: (a) Keinan, E., Greenspoon, N. In Comprehensive Organic Synthesis, Trost, B.M., ed, Permagon: New York, 1991, vol. III, p. 523;
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 523
    • Keinan, E.1    Greenspoon, N.2
  • 33
    • 0002045580 scopus 로고
    • For reviews on the heterolytic activation of elemental hydrogen, see: Brothers, P.J. Prog. Inorg. Chem. 1981, 28, 1.
    • (1981) Prog. Inorg. Chem. , vol.28 , pp. 1
    • Brothers, P.J.1
  • 34
    • 33847797644 scopus 로고
    • Monohydride formation by deprotonation of a dihydride intermediate is known for cationic Rh-complexes: (a) Schrock, R.R., Osborn, J.A. J. Am. Chem. Soc. 1976, 98, 2134;
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 2134
    • Schrock, R.R.1    Osborn, J.A.2
  • 37
    • 37049124551 scopus 로고
    • Direct heterolytic activation of hydrogen by RhCI(CO)(PPh3)2 has been suggested, but likely involves an intermediate dihydride: Evans, D., Osborn, J.A., Wilkinson, G. J. Chem. Soc. A 1968, 3133.
    • (1968) J. Chem. Soc. A , pp. 3133
    • Evans, D.1    Osborn, J.A.2    Wilkinson, G.3
  • 50
    • 0032503512 scopus 로고    scopus 로고
    • and references therein
    • For examples of Rh(III)-enyl complexes, see: Evans, P.A., Nelson, J.D. J. Am. Chem. Soc. 1998, 120, 5581 and references therein.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 5581
    • Evans, P.A.1    Nelson, J.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.