| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5281492 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
N-Acetylindoles can be oxidatively coupled with arenes such as benzene or pentafluorobenzene in dioxane. The use of Cu(OAc)2 as the stoichiometric oxidant produces selective arylation at the 3-position of indole while AgOAc produces selective arylation at indole's 2-position.
Graphical abstractN-Acetylindoles can be oxidatively coupled with arenes such as benzene or pentafluorobenzene in dioxane. The use of Cu(OAc)2 as the stoichiometric oxidant produces selective arylation at the 3-position of indole while AgOAc produces selective arylation at indole's 2-position.Download full-size image
Related Topics
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Authors
Shathaverdhan Potavathri, Ashley S. Dumas, Timothy A. Dwight, Gregory R. Naumiec, Jeffrey M. Hammann, Brenton DeBoef,