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Volumn 11, Issue 18, 2009, Pages 4244-4247

Homogeneous, anaerobic (N-heterocyclic carbene)-Pd or -Ni catalyzed oxidation of secondary alcohols at mild temperatures

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EID: 70349126318     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol901825u     Document Type: Article
Times cited : (45)

References (37)
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    • (b) Muzart, J. Tetrahedron 2003, 59, 5789-5816.
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  • 18
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    • 2 and with the exception of one substrate the best combination required 105°C.
    • 2 and with the exception of one substrate the best combination required 105°C.
  • 21
    • 36849065859 scopus 로고    scopus 로고
    • For general reviews on NHCs, Nolan, S. P., Ed. Wiley-VCH: Weinheim, Germany
    • For general reviews on NHCs, see : (a) Nolan, S. P., Ed. N-Heterocyclic Carbenes in Synthesis; Wiley-VCH: Weinheim, Germany, 2006.
    • (2006) N-Heterocyclic Carbenes in Synthesis
  • 22
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    • Glorius, F., Ed.
    • (b) Glorius, F., Ed. Top. Organomet. Chem. 2007, 21.
    • (2007) Top. Organomet. Chem. , pp. 21
  • 30
    • 0036860845 scopus 로고    scopus 로고
    • For a review in metal-mediated hydrodehalogenation
    • (d) For a review in metal-mediated hydrodehalogenation, see: Alonso, F.; Beletskaya, I. P.; Yus, M. Chem. Rev. 2002, 102, 4009-11091
    • (2002) Chem. Rev. , vol.102 , pp. 4009-11091
    • Alonso, F.1    Beletskaya, I.P.2    Yus, M.3
  • 32
    • 17744365015 scopus 로고    scopus 로고
    • For an excellent, substrate-dependent comparison of Pd-catalyzed aerobic systems
    • For an excellent, substrate-dependent comparison of Pd-catalyzed aerobic systems, see: Schultz, M. J.; Hamilton, S. S.; Jensen, D. R.; Sigman, M. S. J. Org. Chem. 2005, 70, 3343-3352.
    • (2005) J. Org. Chem. , vol.70 , pp. 3343-3352
    • Schultz, M.J.1    Hamilton, S.S.2    Jensen, D.R.3    Sigman, M.S.4
  • 34
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    • 2: $0.05/mmol (Strem catalog 2008)
    • 2: $0.05/mmol (Strem catalog 2008).
  • 36
    • 33845541006 scopus 로고    scopus 로고
    • For a heterogeneous system, with Ni salts and bleach in water
    • (b) For a heterogeneous system, with Ni salts and bleach in water, see: Grill, J. M.; Ogle, J. W.; Miller, S. A. J. Org. Chem. 2006, 71, 9291-9296.
    • (2006) J. Org. Chem. , vol.71 , pp. 9291-9296
    • Grill, J.M.1    Ogle, J.W.2    Miller, S.A.3
  • 37
    • 0037393778 scopus 로고    scopus 로고
    • For a review on this Pd-catalyzed reaction
    • For a review on this Pd-catalyzed reaction, see: Culkin, D. A.; Hartwig, J. F. Acc. Chem. Res. 2003, 36, 234-235.
    • (2003) Acc. Chem. Res. , vol.36 , pp. 234-235
    • Culkin, D.A.1    Hartwig, J.F.2


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