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Volumn 29, Issue 9, 2010, Pages 2098-2103

Synthesis of oxygen- and sulfur-bridged dirhodium complexes and their use as catalysts in the chemoselective hydrogenation of alkenes

Author keywords

[No Author keywords available]

Indexed keywords

AIR-STABLE; CARBON ATOMS; CATALYTIC ACTIVITY; CHEMO-SELECTIVITY; CHEMOSELECTIVE HYDROGENATION; DIRHODIUM COMPLEX; SULFUR-BRIDGED; SYMMETRICAL STRUCTURE; THERMALLY STABLE;

EID: 77951865141     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om100067r     Document Type: Article
Times cited : (16)

References (89)
  • 1
    • 17444395097 scopus 로고    scopus 로고
    • For the review of bimetallic catalysis, see:;;, Eds.; Wiely-VCH Verlag GmbH & Co. KGaA: Weinheim
    • For the review of bimetallic catalysis, see: Multimetallic Catalysts in Organic Synthesis; Shibasaki, M.; Yamamoto, Y., Eds.; Wiely-VCH Verlag GmbH & Co. KGaA: Weinheim, 2004.
    • (2004) Multimetallic Catalysts in Organic Synthesis
    • Shibasaki, M.1    Yamamoto, Y.2
  • 2
    • 0000005135 scopus 로고
    • Catalysis and related reactions with compounds containing heteronuclear metal-metal bonds
    • Abel, E. W.; Willkinson, G.; Stone, F. G. A., Eds.; Elsevier: Oxford, U.K
    • Braunstein, P.; Rose, J. Catalysis and Related Reactions with Compounds Containing Heteronuclear Metal-Metal Bonds. In Comprehensive Organometallic Chemistry II; Abel, E. W.; Willkinson, G.; Stone, F. G. A., Eds.; Elsevier: Oxford, U.K., 1995, Vol. 10, p 351.
    • (1995) Comprehensive Organometallic Chemistry II , vol.10 , pp. 351
    • Braunstein, P.1    Rose, J.2
  • 22
    • 0037243669 scopus 로고    scopus 로고
    • For the review of rhodium-catalyzed reactions, see
    • For the review of rhodium-catalyzed reactions, see: Fagnou, K.; Lautens, M. Chem. Rev. 2003, 103, 169
    • (2003) Chem. Rev. , vol.103 , pp. 169
    • Fagnou, K.1    Lautens, M.2
  • 40
    • 77951800815 scopus 로고    scopus 로고
    • Reduction by heterogeneous catalysis
    • For reviews of transition metal-catalyzed hydrogenation of alkenes, see:;;. In;, Ed.; Georg Thieme Verlag: Stuttgart, NY
    • For reviews of transition metal-catalyzed hydrogenation of alkenes, see: Chessum, N.; Couty, S.; Jones, K. Reduction by Heterogeneous Catalysis. In Science of Synthsis; Hiemstra, H., Ed.; Georg Thieme Verlag: Stuttgart, NY, 2002; Vol. 48, p 275.
    • (2002) Science of Synthsis , vol.48 , pp. 275
    • Chessum, N.1    Couty, S.2    Jones, K.3    Hiemstra, H.4
  • 41
    • 84902431957 scopus 로고    scopus 로고
    • Reduction by homogeneous catalysis or biocatalysis
    • Ed.; Georg Thieme Verlag: Stuttgart, NY
    • Tsukamoto, M.; M. Kitamura, M. Reduction by Homogeneous Catalysis or Biocatalysis. In Science of Synthsis; Hiemstra, H., Ed.; Georg Thieme Verlag: Stuttgart, NY, 2002; Vol. 48, p 341.
    • (2002) Science of Synthsis , vol.48 , pp. 341
    • Tsukamoto, M.1    Kitamura M, M.2    Hiemstra, H.3
  • 42
  • 43
    • 84891031794 scopus 로고    scopus 로고
    • Alkene reduction: Hydrosilylation
    • For review of hydrosilylation, see:;. In;;, Eds.; Wiely-VCH Verlag GmbH & Co. KGaA: Weinheim
    • For review of hydrosilylation, see: Mayes, P. A.; Perlmutter, P. Alkene Reduction: Hydrosilylation. In Modern Reduction Methods; Andersson, P. G.; Munslow, I. J., Eds.; Wiely-VCH Verlag GmbH & Co. KGaA: Weinheim, 2008; p 87.
    • (2008) Modern Reduction Methods , pp. 87
    • Mayes, P.A.1    Perlmutter, P.2    Andersson, P.G.3    Munslow, I.J.4
  • 45
    • 13444310678 scopus 로고    scopus 로고
    • For chemoselective hydrogenation, see
    • For chemoselective hydrogenation, see: Ikawa, T.; Sajiki, H.; Hirota, K. Tetrahedron 2005, 61, 2217
    • (2005) Tetrahedron , vol.61 , pp. 2217
    • Ikawa, T.1    Sajiki, H.2    Hirota, K.3
  • 73
    • 37849027557 scopus 로고    scopus 로고
    • The nitro group is reduced in the normal hydrogenation conditions using palladium complexes as the catalysts; see
    • The nitro group is reduced in the normal hydrogenation conditions using palladium complexes as the catalysts; see: Erion, M. D.; Dang, Q.; Reddy, M. R.; Kasibhatla, S. R.; Huang, J.; Lipscomb, W. N.; Van Poelje, P. D. J. Am. Chem. Soc. 2007, 129, 15480
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 15480
    • Erion, M.D.1    Dang, Q.2    Reddy, M.R.3    Kasibhatla, S.R.4    Huang, J.5    Lipscomb, W.N.6    Van Poelje, P.D.7
  • 75
    • 0015217113 scopus 로고
    • The benzyl group is used as the protecting group for hydroxy compounds and easily removed in hydrogenation conditions; see
    • The benzyl group is used as the protecting group for hydroxy compounds and easily removed in hydrogenation conditions; see: Buchi, G.; Weinreb, S. M. J. Am. Chem. Soc. 1971, 93, 746
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 746
    • Buchi, G.1    Weinreb, S.M.2


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