Abstract
The Ugi-Smiles and Passerini-Smiles couplings are extensions of Ugi and Passerini reactions involving the use of acidic phenols in place of the traditional carboxylic acid partners. A Smiles rearrangement is in each case responsible for the final N-aryl carboxamide formation. All the available data on the mechanisms and the scope of these reactions are presented. To demonstrate the interest of Ugi-Smiles and Passerini-Smiles couplings, these reactions have been further applied to the preparation of various fused heterocyclic systems. These "post-condensation" studies are also covered in this review.
| Original language | English |
|---|---|
| Pages (from-to) | 7749-7762 |
| Number of pages | 14 |
| Journal | European Journal of Organic Chemistry |
| Volume | 2014 |
| Issue number | 35 |
| DOIs | |
| Publication status | Published - 20 Oct 2014 |
| Externally published | Yes |
Keywords
- Isocyanides
- Molecular diversity
- Multicomponent reactions
- Phenols
- Reaction mechanisms
- Rearrangement
- Synthetic methods
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