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Volumn 9, Issue 26, 2007, Pages 5489-5492

α-arylation of ketones using highly active, air-stable (DtBPF)PdX2 (X = Cl, Br) catalysts

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EID: 38349133083     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702430a     Document Type: Article
Times cited : (108)

References (37)
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    • (2004) Metal-Catalyzed Cross-Coupling Reactions
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    • Diederich, F, Stang, P. J, Eds, VCH: Weinheim, Germany
    • (d) Metal-Catalyzed Cross-Coupling Reactions; Diederich, F., Stang, P. J., Eds.; VCH: Weinheim, Germany, 1998.
    • (1998) Metal-Catalyzed Cross-Coupling Reactions
  • 18
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    • (a) Ferrocenes; Togni, A., Hayashi, T., Eds.; VCH: Weinheim, Germany, 1995.
    • (1995) Togni, A
    • Ferrocenes1
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    • 38349106062 scopus 로고    scopus 로고
    • Ferrocenes: From Materials and Chemistry to Biology; Wiley: Chichester, UK
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    • (b) Stepnicka, P. Ferrocenes: From Materials and Chemistry to Biology; Wiley: Chichester, UK, in press.
    • Stepnicka, P.1
  • 20
    • 38349161541 scopus 로고    scopus 로고
    • Ferrocenes: From Materials and Chemistry to Biology; Wiley: Chichester, UK
    • in press
    • (a) Colacot. T. J.; Parísel, S. Ferrocenes: From Materials and Chemistry to Biology; Wiley: Chichester, UK, in press.
    • Colacot, T.J.1    Parísel, S.2
  • 21
    • 0042238447 scopus 로고    scopus 로고
    • Colacot, T. J. Chem Rev. 2003, 103, 3101 (see references therein).
    • (b) Colacot, T. J. Chem Rev. 2003, 103, 3101 (see references therein).
  • 26
    • 0007121042 scopus 로고    scopus 로고
    • 2: P-Pd-P = 103.59°: Elsagir, A. R.; Gassner. F.; Gorls, H.; Dinjus, E. J. Organomet. Chem. 2000, 597, 139.
    • 2: P-Pd-P = 103.59°: Elsagir, A. R.; Gassner. F.; Gorls, H.; Dinjus, E. J. Organomet. Chem. 2000, 597, 139.
  • 27
    • 38349164313 scopus 로고    scopus 로고
    • DCyPF-PdCl2: P-Pd-P, 102.45°: see ref 10
    • 2: P-Pd-P = 102.45°: see ref 10.
  • 28
    • 14844297339 scopus 로고    scopus 로고
    • 2: P-Pd-P = 99.3°: Bianchini, C.; Meli, A.; Oberhauser, W.; Parisel, S.; Passaglia, E.; Ciardelli, F.; Gusev, O. V.; Kal'sin, A. M.; Vologdin, N. V. Organometallics 2005, 24, 1018.
    • 2: P-Pd-P = 99.3°: Bianchini, C.; Meli, A.; Oberhauser, W.; Parisel, S.; Passaglia, E.; Ciardelli, F.; Gusev, O. V.; Kal'sin, A. M.; Vologdin, N. V. Organometallics 2005, 24, 1018.
  • 29
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    • 2: P-Pd-P = 97.98°: Butler, I. R.; Cullen, W. R.; Kim, T. J.; Rettig, S. J.; Trotter, J. Organometallics 1985, 4, 972.
    • 2: P-Pd-P = 97.98°: Butler, I. R.; Cullen, W. R.; Kim, T. J.; Rettig, S. J.; Trotter, J. Organometallics 1985, 4, 972.
  • 35
    • 38349120915 scopus 로고    scopus 로고
    • 3 with DtBPF at different stoichiometrics.
    • 3 with DtBPF at different stoichiometrics.
  • 37
    • 0034327037 scopus 로고    scopus 로고
    • 2 due to DtBPF cleavage under catalytic α-arylation conditions was observed. For DtBPF cleavage under O-arylation conditions, see: Shelby, Q.; Kataoka, N.; Mann. G.; Hartwig, J. F. J. Am. Chem Soc. 2000, 122, 10718.
    • 2 due to DtBPF cleavage under catalytic α-arylation conditions was observed. For DtBPF cleavage under O-arylation conditions, see: Shelby, Q.; Kataoka, N.; Mann. G.; Hartwig, J. F. J. Am. Chem Soc. 2000, 122, 10718.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.