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
Hauptverfasser: Barnea, Eyal, Andrea, Tamer, Kapon, Moshe, Berthet, Jean-Claude, Ephritikhine, Michel, Eisen, Moris S
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Sprache:eng
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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
ISSN:0002-7863
1520-5126
DOI:10.1021/ja046604a