Regiocontrolled preparation of 3-acyl-6-aryl-2-pyridones via condensation of 3-aryl-3-chloropropeniminium salts with β-keto-amides
✍ Scribed by Thouraya Gmiza; Mohamed Adnen Hadj Ayed; Jamel Eddine Khiari; Béchir Ben Hassine
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- French
- Weight
- 231 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
3,6-Disubstituted pyridin-2-ones a b s t r a c t F series of substituted 3-acyl-6-aryl-2-pyridones have been prepared in one-step reactions via condensation of 3-aryl-3-chloropropeniminium salts with b-keto-amides. This efficient synthesis has the advantages of high yields and simple reaction procedures.
📜 SIMILAR VOLUMES
Heck arylation of N-acyl-3-pyrrolines and an N-acyl-tetrahydropyridine with aryldiazonium tetrafluoroborates under phosphine-free conditions proceeded smoothly to give a-hydroxycarbamates (hemiaminals) or a-alkoxycarbamates which were oxidized to the desired gand d-lactams. Acidic hydrolysis of the