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Volumn 62, Issue 9, 2009, Pages 983-987

Synthesis and structural characterization of palladium dicarbene complexes bearing labile co-ligands

Author keywords

[No Author keywords available]

Indexed keywords

CO-LIGANDS; DIPHOSPHINES; DISPROPORTIONATIONS; HYDROAMINATIONS; LIGAND INFLUENCE; METATHESIS REACTIONS; SINGLE CRYSTAL X-RAY DIFFRACTION; SPECTROMETRIC METHODS; STRUCTURAL CHARACTERIZATION;

EID: 70349309932     PISSN: 00049425     EISSN: None     Source Type: Journal    
DOI: 10.1071/CH09143     Document Type: Conference Paper
Times cited : (20)

References (21)
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  • 8
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    • Synthesis of benzannulated N-heterocyclic carbene ligands by a template synthesis from 2-nitrophenyl isocyanide
    • DOI 10.1002/chem.200400576
    • F. E. Hahn, C. G. Plumed, M. Münder, T. Lügger, Chem. Eur. J. 2004, 10 , 6285. doi:10.1002/CHEM.200400576 (Pubitemid 40018297)
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    • Hahn, F.E.1    Plumed, C.G.2    Munder, M.3    Lugger, T.4
  • 9
    • 34447258605 scopus 로고    scopus 로고
    • Pd(II) complexes of a sterically bulky, benzannulated N-heterocyclic carbene and their catalytic activities in the Mizoroki-Heck reaction
    • DOI 10.1016/j.jorganchem.2007.04.037, PII S0022328X07003300
    • Y. Han, H. V. Huynh, L. L. Koh, J. Organomet. Chem. 2007, 692, 3606. doi:10.1016/J.JORGANCHEM.2007.04.037 (Pubitemid 47042802)
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    • Han, Y.1    Huynh, H.V.2    Koh, L.L.3
  • 10
    • 33644926388 scopus 로고    scopus 로고
    • Mixed dicarboxylato - Bis(carbene) complexes of palladium(II): Synthesis, structures, trans - Cis isomerism, and catalytic activity
    • DOI 10.1021/om0510369
    • H. V. Huynh, T. C. Neo, G. K. Tan, Organometallics 2006, 25, 1298. doi:10.1021/OM0510369 (Pubitemid 43382905)
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    • Huynh, H.V.1    Neo, T.C.2    Tan, G.K.3
  • 11
    • 23844456602 scopus 로고    scopus 로고
    • Solvent-controlled selective synthesis of a trans-configured benzimidazoline-2-ylidene palladium(II) complex and investigations of its Heck-type catalytic activity
    • DOI 10.1016/j.jorganchem.2005.04.053, PII S0022328X0500402X
    • H. V. Huynh, J. H. H. Ho, T. C. Neo, L. L. Koh, J. Organomet. Chem. 2005, 690, 3854. doi:10.1016/J.JORGANCHEM.2005.04.053 (Pubitemid 41162577)
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  • 15
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    • The preparation of complex 1 by a different route with a lower yield of 58% has recently been reported: doi:10.1002/ADSC.200700271
    • (a) The preparation of complex 1 by a different route with a lower yield of 58% has recently been reported: A. Biffis, C. Tubaro, G. Buscemi, M. Basato, Adv. Synth. Catal. 2008, 350, 189. doi:10.1002/ADSC.200700271
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 189
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  • 16
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    • The diiodo analogue of 1 has also been reported: doi:10.1016/S0022- 328X(99)00219-3
    • (b) The diiodo analogue of 1 has also been reported: F. E. Hahn, M. Foth, J. Organomet. Chem. 1999, 585, 241. doi:10.1016/S0022-328X(99)00219-3
    • (1999) J. Organomet. Chem. , vol.585 , pp. 241
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    • (Bruker AXS Inc.: Madison, Wisconsin, USA).
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    • Bruker AXS Inc.: Madison, Wisconsin, USA
    • SAINT + version 6.22a 2001 (Bruker AXS Inc.: Madison, Wisconsin, USA).
    • (2001) SAINT + Version 6.22a


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