## Abstract The ring transformation of 2H‐pyran‐2‐ones by N‐aryl amidines is strongly influenced by the amidine substituents and leads to title compounds of type (III).
✦ LIBER ✦
Facile synthesis of 2,6-diaryl-4-secondary aminonicotinonitriles and highly substituted unsymmetrical 2,2′-bipyridines
✍ Scribed by Sidhanath V. Bhosale; Umesh D. Patil; Mohan B. Kalyankar; Santosh V. Nalage; Vijay S. Patil; Kamlesh R. Desale
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2010
- Tongue
- English
- Weight
- 123 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.380
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
magnified image
The ring transformation of 2H‐pyran‐2‐one by N‐aryl amidine in the presence of KOH in DMF at room temperature resulted in a facile synthesis of the 2,6‐diaryl‐4‐secondary aminonicotinonitrile and highly substituted unsymmetrical 2,2′‐bipyridines in moderate yield. J. Heterocyclic Chem., (2010).
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