Abstract
Two different Ugi-Smiles post-condensations strategies have been used for new three and four-component formation of quinoxaline scaffolds. In the first approach, a one-pot hydrogenation-cyclization affords the heterocycle with loss of the initial isocyanide moiety. In the second one, the use of o-iodonitrophenol as starting phenol, coupled with copper catalyzed cyclization gave us similar quinoxaline derivatives resulting from a four coupling.
| Original language | English |
|---|---|
| Pages (from-to) | 503-517 |
| Number of pages | 15 |
| Journal | Heterocycles |
| Volume | 73 |
| Issue number | C |
| DOIs | |
| Publication status | Published - 1 Jan 2007 |
| Externally published | Yes |
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