| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5216443 | Tetrahedron | 2014 | 7 Pages |
Abstract
An acid-catalyzed modular synthesis of substituted 5H-dibenz[c,e]azepines from a biaryl allylbenzamides prepared from the MBH adducts via a cascade dearoylation and intramolecular cyclization is described. The utility of the product for preparing 7,9-dihydro-4bH-dibenz[c,e]pyrrolo[1,2-a]azepine is also presented.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
![First Page Preview: An alternate route to substituted 6,7-dihydro 5H-dibenz[c,e]azepines from allylbenzamides derived from the Morita–Baylis–Hillman adducts An alternate route to substituted 6,7-dihydro 5H-dibenz[c,e]azepines from allylbenzamides derived from the Morita–Baylis–Hillman adducts](/preview/png/5216443.png)