Abstract
Diverse N-(heteroarylmethyl)anilines were easily prepared from corresponding aldimines derived from commercially available aromatic aldehydes and anilines. New series of substituted NH-tetrahydroquinolines were also prepared using imino-Diels-Alder reaction between aldimines and N-vinylpyrrolidin-2-one in the presence of BF3OEt2 and the multi-component condensation reactions using a friendly ecological catalyst (BiCl3). The secondary amines obtained bearing a heteroaryl moiety were tested as possible antibacterial and antifungal agents.
| Original language | English |
|---|---|
| Pages (from-to) | 319-325 |
| Number of pages | 7 |
| Journal | Journal of the Chilean Chemical Society |
| Volume | 49 |
| Issue number | 4 |
| DOIs | |
| State | Published - Dec 2004 |
| Externally published | Yes |
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