Abstract
The Passerini–Smiles reactions of α-ketophosphonates with nitrophenols has been used as a platform to observe complex cascades involving multiple Smiles transfers coupled with phospha-Brook rearrangement. When using 4-nitrophenols a rare 1,3-Truce–Smiles rearrangement is observed leading to diarylacetamide derivatives. 2-Nitro-derivatives lead to a completely different reactivity pattern that may be explained by a nitro to nitroso conversion followed by a σ–π metathesis. All mechanistic assumptions are confirmed by DFT calculations performed on both families of adducts. The potential of this work has been further demonstrated by the use of N-aryl α-ketoamides as alternative starting materials for these cascades as well as the disclosure of new aza-Nazarov access to hydroxy-indolones.
| Original language | English |
|---|---|
| Article number | e202116249 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 61 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - 7 Mar 2022 |
| Externally published | Yes |
Keywords
- Cyclizations
- Heterocycles
- Reaction Mechanisms
- Rearrangements
- Smiles Reaction
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