| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5222533 | Tetrahedron | 2011 | 10 Pages |
Abstract
Diels–Alder cycloadditions of in situ-generated, substituted 2,2-dimethoxycyclohexa-3,5-dienones with olefinic dienophiles resulted in the development of an efficient method for the preparation of highly functionalized bicyclo[2.2.2]oct-5-en-2-ones with good to excellent yields.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
![First Page Preview: Facile preparation of bicyclo[2.2.2]octenone derivatives via Diels–Alder cycloadditions of in situ-generated masked o-benzoquinones Facile preparation of bicyclo[2.2.2]octenone derivatives via Diels–Alder cycloadditions of in situ-generated masked o-benzoquinones](/preview/png/5222533.png)