## 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
✦ LIBER ✦
Further Enolate Alkylation Studies of 2,5-Dimethyl-3(2H)-furanone.
✍ Scribed by Drury S. Caine; Mark E. Arant
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 24 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
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