| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275276 | Tetrahedron Letters | 2008 | 5 Pages |
Abstract
Ruthenium-catalyzed regioselective ring-opening of aliphatic and aryl epoxides under solvent-free conditions is reported. It was found that RuCl3·nH2O catalyzes the Friedel-Crafts alkylation of indoles, providing 3-alkylated derivatives in good yields under mild reaction conditions.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
K. Tabatabaeian, M. Mamaghani, N.O. Mahmoodi, A. Khorshidi,