| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5268985 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
Microwave-irradiated Diels-Alder reactions of anthracene and endoxides (6a-g) in water afforded the cycloadducts (8a-g) with high efficiencies. The extended triptycenes (2a-g) were readily obtained by dehydration of 8a-g in a mixture of AcOH and Ac2O with good overall yields.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Bao-Jian Pei, Albert W.M. Lee,