Room Temperature Ring-Opening Metathesis of Pyridines by a Transient TiC Linkage.

The article cites a study that reports on the facile and nonreductive C—N activation and cleavage of pyridine by a transient titanium alkylidyne. Activation of the C—N bond in pyridine involves a unique process, a ring-opening metathesis step invoking the cycloadition of the aromatic C=N bond across...

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Bibliographic Details
Published in:Journal of the American Chemical Society Vol. 128; no. 21; pp. 6798 - 6800
Main Authors: Bailey, Brad C., Hongjun Fan, Huffman, John C., Mu-Hyun Baik, Mindiola, Daniel J.
Format: Article
Published: American Chemical Society 5/31/2006
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Online Access:View this record in EBSCOhost
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Summary:The article cites a study that reports on the facile and nonreductive C—N activation and cleavage of pyridine by a transient titanium alkylidyne. Activation of the C—N bond in pyridine involves a unique process, a ring-opening metathesis step invoking the cycloadition of the aromatic C=N bond across a reactive TiΞC'Bu linkage. The combination of synthesis, isotopic labeling and theoretical studies allowed for understanding this rare transformation.