Abstract
A new method of FeCl2-catalyzed [4+2] annulation of α,β-unsaturated ketoxime acetates with N-acetyl enamides in batch and flow is reported. The current strategy features low-cost catalytic system, use of electron-rich olefins, operational simplicity, and broad substrate scope, thus providing a facile and efficient access to substituted pyridines in moderate to good yields.
Original language | English |
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Pages (from-to) | 283-287 |
Number of pages | 5 |
Journal | Synlett |
Volume | 33 |
Issue number | 3 |
DOIs | |
State | Published - Feb 2022 |
Keywords
- N -acetyl enamides
- annulation
- iron
- ketoxime acetates
- pyridines