期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 13, 期 26, 页码 7466-7478出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.200601822
关键词
C-H activation; cobalt; cycloaddition; density functional calculations; N-H activation
DFT computations have been executed aimed at illuminating the variety of pathways by which pyridones react with alkynes in the presence of [CpCoL2]: NH-2-pyridones furnish N-dienylated ligands (N-H activation pathway), N-methyl-2-pyridones are converted into ligated cyclohexadienes ([2+2+2] cocycloaddition pathway), and N-alkynyl-2-pyridones may undergo either [2+2+2] cocycloaddition or C-dienylation (C-H activation), depending on the length of the tether.The calculations predict the formation of the experimentally observed products, including their regio- and stereochemical make up. In addition, the unusual regiochemical outcome of the all-intramolecular [2+2+2] cycloaddition of N,N '-dipentynylpyrazinedione was rationalized by computation, which led to the discovery of a new mechanism.
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