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Issue 4, 1994
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Transfer of the carbyne ligand to the C[triple bond, length half m-dash]C bond versus alkyne–carbyne–CO coupling in the reactions of [(η5-C5H5)(CO)2Mn[triple bond, length half m-dash]CPh]+ with electron-rich alkynes

Abstract

The carbyne cation [(η5-C5H5)(CO)2Mn[triple bond, length half m-dash]CPh]+1 reacts with bis(diorganylamino)acetylenes by transfer of the carbyne ligand to the C–C bond of the alkynes to give cyclopropenyl cations; in contrast, the reaction with diorganylaminopropyne affords novel η4-carbene complexes by regioselective coupling of the carbyne and one CO ligand with the alkyne.

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Article type: Paper
DOI: 10.1039/C39940000457
Citation: J. Chem. Soc., Chem. Commun., 1994,0, 457-458
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    Transfer of the carbyne ligand to the C[triple bond, length half m-dash]C bond versus alkyne–carbyne–CO coupling in the reactions of [(η5-C5H5)(CO)2Mn[triple bond, length half m-dash]CPh]+ with electron-rich alkynes

    H. Fischer and C. Troll, J. Chem. Soc., Chem. Commun., 1994, 0, 457
    DOI: 10.1039/C39940000457

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