| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5273486 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
Studies on the Friedel–Crafts reaction between carbonyl bicyclic cyclopropane and electronic-rich aromatic systems were conducted. Lewis acid and iminium cationic activation methods were examined. It was found that the cyclopropane ring-opening was highly dependent on the nature of the counter nucleophile as well as the activation method.
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