2,6-Diaryl-4,4-disubstituted-4H-thiopyran: Source for spiro heterocycles
✍ Scribed by Venkatapuram Padmavathi; Akula Balaiah; Dandu Bhaskar Reddy
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2002
- Tongue
- English
- Weight
- 63 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
The 1,5‐diaryl‐3,3‐disubstituted‐1,5‐pentanedione on reaction with ammonium acetate, phosphorus pentoxide and phosphorus pentasulfide gave respective 1,4‐dihydropyridine, 4__H__‐pyran and 4__H__‐thiopyran. Novel spiro heterocycles have been obtained by the cyclocondensation of 4__H__‐thiopyran with hydrazine, hydroxylamine, urea and thiourea.
📜 SIMILAR VOLUMES
## Abstract Novel spiro heterocycles (**__5–12__**) were obtained by the cyclocondensation of 2,6‐diaryl‐4,4‐dimethoxycarbonyl‐/4‐cyano‐4‐ethoxycarbonyl‐1,4‐dihydropyridines(**__3/4__**) with hydrazine hydrate, hydroxylamine hydrochloride, urea, and thiourea. All the compounds were characterized by
## Abstract Novel spiro heterocycles, substituted spiro‐pyrimidine, pyrazole and isoxazole compounds are prepared by the cyclocondensation of 4‐oxocyclohexane __gem__‐dicarboxylates and cyano esters with nucleophiles.