Catalytic Coupling of Terminal Alkynes with Isonitriles Promoted by Organoactinide Complexes
The coupling reaction of terminal alkynes and tert-butylisonitrile to yield substituted α,β-acetylenic aldimines is catalyzed by the organoactinide neutral complexes Cp*2AnMe2 (Cp* = C5Me5, An = Th, U) and the cationic complex [(Et2N)3U][BPh4]. The reaction proceeds by a 1,1-insertion of the isonitr...
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Veröffentlicht in: | Journal of the American Chemical Society 2004-09, Vol.126 (35), p.10860-10861 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | The coupling reaction of terminal alkynes and tert-butylisonitrile to yield substituted α,β-acetylenic aldimines is catalyzed by the organoactinide neutral complexes Cp*2AnMe2 (Cp* = C5Me5, An = Th, U) and the cationic complex [(Et2N)3U][BPh4]. The reaction proceeds by a 1,1-insertion of the isonitrile into the metal−acetylide bond. Additional insertion products can be obtained by altering the catalyst and the reactant ratios. A plausible mechanism for the catalytic reaction is presented, in addition to the crystal structure of Cp*2UMe2 |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja046604a |