## Abstract magnified image Ring closure of 2‐__N__‐benzylamino‐3‐aroylpropionic acids (**3**) with acetic anhydride afforded 3‐__N__‐benzylamino‐5‐aryl‐2(3__H__)‐furanones (**4**). The reaction of the furanones (**4**) with benzylamine in benzene was found to be time dependent. Thus refluxing the
Behavior of 3-Benzylamino-5-aryl-2(3H)-furanones Towards Some Nitrogen Nucleophiles.
✍ Scribed by Kamal A. Kandeel; Ahmed S. A. Youssef; Wael S. I. Abou-Elmagd; Ahmed I. Hashem
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 30 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
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## Abstract 3(2‐pyridinylmethylene)‐5‐aryl‐2(3__H__)‐furanones and 3(3‐pyridinylmethylene)‐5‐aryl‐2(3__H__)‐furanones were prepared as a mixture of (E) and (Z) stereoisomers by condensing pyridine‐2‐carboxaldehyde and pyridine‐3‐carboxaldehyde with 3‐aroylpropionic acids. The reaction of the furano
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