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Volumn 38, Issue 43, 1997, Pages 7603-7604

Sm or Zn-induced coupling reactions. A facile route to 1,2-diketones

Author keywords

[No Author keywords available]

Indexed keywords

DIKETONE;

EID: 0030838725     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)01804-2     Document Type: Article
Times cited : (18)

References (21)
  • 1
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    • Recent reviews: (a)
    • Recent reviews: (a) Molander, G.A., Chem. Rev., 1992, 92, 29.
    • (1992) Chem. Rev. , vol.92 , pp. 29
    • Molander, G.A.1
  • 2
    • 0000421996 scopus 로고
    • (b) Trost, B.M., Fleming, I., Eds. Pergamon: Oxford
    • (b) Inamoto, T., In Comprehensive Organic Synthesis.; Trost, B.M., Fleming, I., Eds. Pergamon: Oxford, 1991, Vol. 4, pp 231-250.
    • (1991) In Comprehensive Organic Synthesis , vol.4 , pp. 231-250
    • Inamoto, T.1
  • 5
    • 33751386286 scopus 로고
    • For the deoxygenation of sulfoxides and epoxides see
    • For the deoxygenation of sulfoxides and epoxides see: Hasegawa, E., Curran, D.P., J. Org. Chem., 1993, 58, 5008;
    • (1993) J. Org. Chem. , vol.58 , pp. 5008
    • Hasegawa, E.1    Curran, D.P.2
  • 7
    • 33751386648 scopus 로고
    • For the organohalo compounds see
    • For the organohalo compounds see: Wipf, P., Venkatraman, S., J. Org. Chem., 1993, 58, 3455;
    • (1993) J. Org. Chem. , vol.58 , pp. 3455
    • Wipf, P.1    Venkatraman, S.2
  • 9
    • 0001490955 scopus 로고
    • For the homocoupling of allylic or benzylic halides see
    • For the homocoupling of allylic or benzylic halides see: Collin, J., Namy, J.L., Dallemer, F., Kagan, H.B., J. Org. Chem., 1991, 56, 3118.
    • (1991) J. Org. Chem. , vol.56 , pp. 3118
    • Collin, J.1    Namy, J.L.2    Dallemer, F.3    Kagan, H.B.4
  • 13
    • 0004063347 scopus 로고
    • Using pyrophoric lead see
    • Using pyrophoric lead see: Meszaros, L., Tetrahedron Lett., 1967, 4951;
    • (1967) Tetrahedron Lett. , pp. 4951
    • Meszaros, L.1
  • 17
    • 84986409344 scopus 로고
    • Zibuck, R., Seebach, D., Helv. Chim. Acta., 1988, 71, 237; For using zerovalent complexes of nickel see: Flood, T.C., Tetrahedron Lett., 1977, 3861.
    • (1988) Helv. Chim. Acta. , vol.71 , pp. 237
    • Zibuck, R.1    Seebach, D.2
  • 18
    • 0002510696 scopus 로고
    • For using zerovalent complexes of nickel see
    • Zibuck, R., Seebach, D., Helv. Chim. Acta., 1988, 71, 237; For using zerovalent complexes of nickel see: Flood, T.C., Tetrahedron Lett., 1977, 3861.
    • (1977) Tetrahedron Lett. , pp. 3861
    • Flood, T.C.1
  • 20
    • 37049040965 scopus 로고
    • Such type of dimerisation of photochemically prepared acyl radicals has been reported see
    • Such type of dimerisation of photochemically prepared acyl radicals has been reported see: Barton, D.H.R., George, M.V., Tomoeda, M., J. Chem. Soc., 1962, 17, 1967; For nucleophilic acylation see: Lapkin, I.I., Anvarovs, G.Y., Povarnltsyna, T.N., J. Gen. Chem., USSR. (English trans) 1966, 36, 1945.
    • (1962) J. Chem. Soc. , vol.17 , pp. 1967
    • Barton, D.H.R.1    George, M.V.2    Tomoeda, M.3
  • 21
    • 37049040965 scopus 로고
    • For nucleophilic acylation see
    • Such type of dimerisation of photochemically prepared acyl radicals has been reported see: Barton, D.H.R., George, M.V., Tomoeda, M., J. Chem. Soc., 1962, 17, 1967; For nucleophilic acylation see: Lapkin, I.I., Anvarovs, G.Y., Povarnltsyna, T.N., J. Gen. Chem., USSR. (English trans) 1966, 36, 1945.
    • (1966) J. Gen. Chem., USSR. (English Trans) , vol.36 , pp. 1945
    • Lapkin, I.I.1    Anvarovs, G.Y.2    Povarnltsyna, T.N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.