Sequential oxopyridinium betaine cycloaddition–palladium catalysed cyclisation–anion capture processes
-
Add time:08/06/2019 Source:sciencedirect.com
Katritzky's oxopyridinium betaine cycloaddition is employed to generate bridged bicyclic substrates suitable for our palladium(0) catalysed cyclisation–anion capture methodology. A variety of polycyclic heterocycles have been synthesised via monocyclisation–organotin(IV) capture with or without incorporation of carbon monoxide. Sequential cycloaddition–cyclisation can be performed as a one pot process to deliver substantial gain in molecular complexity.
We also recommend Trading Suppliers and Manufacturers of 2-oxopyridinium chloride (cas 13472-62-3). Pls Click Website Link as below: cas 13472-62-3 suppliers
Prev:Tautomers of N-ethyl-3-oxopyridinium and its adduct with squaric acid studied by X-ray, Raman, FTIR, NMR and DFT methods
Next:Preparation, spectroscopic and antibacterial studies on charge-transfer complexes of 2-hydroxypyridine with picric acid and 7,7′,8,8′-tetracyano-p-quinodimethane) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Preparation, spectroscopic and antibacterial studies on charge-transfer complexes of 2-hydroxypyridine with picric acid and 7,7′,8,8′-tetracyano-p-quinodimethane08/07/2019
- Tautomers of N-ethyl-3-oxopyridinium and its adduct with squaric acid studied by X-ray, Raman, FTIR, NMR and DFT methods08/05/2019


