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0000064895
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(a) van Koten et al. have successfully employed a NCN-type nickelpincer complex for the Kharasch reaction. For a review, see: Gossage, R. A.; van de Kuil, L. A.; van Koten, G. Acc. Chem. Res. 1998, 31, 423.
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24944543806
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(b) Recently, thiolation of iodobenzene catalyzed by a NNN-type nickel-pincer complex was reported; see: Baldovino-Pantaleon, O.; Hernandez-Ortega, S.; Morales-Morales, D. Inorg. Chem. Commun. 2005, 8, 955.
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27
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33745788537
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Carbene precursor 1 was prepared according to Crabtree's method; see ref 3c
-
Carbene precursor 1 was prepared according to Crabtree's method; see ref 3c.
-
-
-
-
28
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33745774952
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note
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2, 49%.
-
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-
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29
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33745797854
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note
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2/1. Detailed studies to reveal the origin of the difference in catalytic activity between two catalyst systems are underway and will be reported in due course.
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-
-
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30
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24044443121
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(a) Foley, P.; DiCosimo, R.; Whitesides, G. M. J. Am. Chem. Soc. 1980, 102, 6713.
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Eberhard suggested the possibility of formation of metallic Pd(0) from a PCP-type pincer ligand; see: Eberhard, M. R. Org. Lett. 2004, 6, 2125.
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Eberhard, M.R.1
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35
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20544478113
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For the synthesis of a heterogeneous Ni-nanoparticle and its use for Heck reaction of iodobenzenes, see: Houdayer, A.; Schneider, R.; Billaud, D.; Ghanbaja, J.; Lambert, J. Synth. Met. 2005, 151, 165.
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Lambert, J.5
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36
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note
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13C NMR spectrum of complex 2 could not be obtained due to its insolubility in various deuterated solvents.
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