## 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
ChemInform Abstract: Behavior of 3(2-Pyridinylmethylene)-5-aryl-2(3H)-furanones and 3(3-Pyridinylmethylene)-5-aryl-2(3H)-furanones as Alkylating Agents: A Comparative Study.
✍ Scribed by Wael S. I. Abou Elmagd
- Book ID
- 112043165
- Publisher
- John Wiley and Sons
- Year
- 2012
- Weight
- 30 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
## 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
## Abstract 3,4‐Dichloro‐2(5__H__)‐furanone, which has been prepared efficiently from mucochloric acid, has been transformed selectively into 4‐aryl‐3‐chloro‐2(5__H__)‐furanones either by Suzuki‐ or Stille‐type reactions. These monochloro derivatives have been used as precursors either to (__Z__)‐4