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Volumn 48, Issue 16, 2009, Pages 2937-2940

Nickel-catalyzed cross-coupling of non-activated and functionalized alkyl halides with alkyl grignard reagents

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL HALIDES; CROSS COUPLING REACTIONS; CROSS-COUPLINGS; FUNCTIONALIZED; GRIGNARD REAGENT;

EID: 70349778999     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200806138     Document Type: Article
Times cited : (159)

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    • Similar results are obtained when the reactions are conducted at -35 °C for 30 min or when the reagents are mixed at -35 °C and then the reaction mixtures are warmed up over a 30 min time period.
    • Similar results are obtained when the reactions are conducted at -35 °C for 30 min or when the reagents are mixed at -35 °C and then the reaction mixtures are warmed up over a 30 min time period.
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    • We notice that alkyl iodides and bromides react at comparable rates under these conditions. A particular alkyl iodide or bromide is chosen according to its availability or preparation procedures
    • We notice that alkyl iodides and bromides react at comparable rates under these conditions. A particular alkyl iodide or bromide is chosen according to its availability or preparation procedures.
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    • II-ligand diradical, for simplicity, the formal oxidation state of Ni is represented as + 4 without implying its true electronic structure. Pincer amido ligands might be redox-active, see: D. Adhikari, S. Mossin, F.. Basuli, J. C. Huffman, R. K. Szilagyi, K. Meyer, D. J. Mindiola,J. Am. Chem. Soc. 2008,130, 3676-3682.
    • II-ligand diradical, for simplicity, the formal oxidation state of Ni is represented as + 4 without implying its true electronic structure. Pincer amido ligands might be redox-active, see: D. Adhikari, S. Mossin, F.. Basuli, J. C. Huffman, R. K. Szilagyi, K. Meyer, D. J. Mindiola,J. Am. Chem. Soc. 2008,130, 3676-3682.


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