| نویسندگان | Safaei-Ghomi J., Salimi F., Ramazani A., Zeinali Nasrabadi F., Ahmadi Y. |
| نشریه | Turkish Journal of Chemistry |
| كد DOI/DOR | 10.3906/kim-1109-40 |
| تاریخ انتشار | ۲۰۱۲ |
چکیده مقاله
A 3-component domino reaction approach between a primary amine, a dialkyl acetylenedicarboxylate, and 2-oxo-2-phenylacetaldehyde that affords novel alkyl 2-benzoyl-4-alkylamino-5-oxo-2,5-dihydro-3-furan carboxylate derivatives is reported. The reaction sequence consists of an initial Michael addition of primary amines to dialkyl acetylenedicarboxylates, followed by an aldol-like reaction with 2-oxo-2-phenylacetaldehyde, and then λ-lactonization to afford the products. This cascade reaction sequence represents a rapid and unprecedented route to the described biologically interesting molecules. © TÜBITAK.
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