| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5212324 | Tetrahedron | 2017 | 6 Pages |
Abstract
A highly regioselective and diastereoselective oxa-Diels-Alder reaction catalyzed by AlCl3 has been developed. This reaction is efficient and characterized by good functional group compatibility, F, Cl, CN, NO2, OMe and thiophenyl groups are tolerated. A Lewis acid catalyzed concerted cycloaddition mechanism is proposed based on the results.
Graphical abstractDownload high-res image (88KB)Download full-size image
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Wujun Jian, Bo Qian, Hongli Bao, Daliang Li,