| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5263213 | Tetrahedron Letters | 2013 | 6 Pages |
Abstract
A facile method for the regioselective synthesis of tetrasubstituted pyrroles, from readily accessible 1,3-dicarbonyls, benzoin derivatives and ammonium acetate, has been developed. The one-pot three-component reactions were performed to afford tetrasubstituted pyrroles under solvent- and catalyst-free conditions.
Related Topics
Physical Sciences and Engineering
Chemistry
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Authors
Subrahmanya Ishwar Bhat, Darshak R. Trivedi,