Intramolecular C-H insertion in ring-expanded N-heterocyclic carbenes
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Mild heating of the ring-expanded N-heterocyclic Carbenes 7-Mes and 6-Mes results in intramolecular insertion of the carbene into an ortho-methyl C-H bond. In the presence of traces of acid, the resulting products ring-open to afford N-alkyl indoles. (C) 2009 Elsevier Ltd. All rights reserved.
|Creators||Holdroyd, R. S., Page, M. J., Warren, M. R. and Whittlesey, M. K.|
|Departments||Faculty of Science > Chemistry|
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