| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5219834 | Tetrahedron | 2012 | 5 Pages |
Abstract
An efficient synthetic method for the pentasubstituted pyrroles was successfully developed via the one-pot domino reactions of arylamines, acetylenedicarboxylates, and 3-phenacylideneoxindoles. The reaction mechanism involved the sequential Michael addition and ring closure of the in situ generated β-active enamino ester.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
