C5-Alkyl-1,3,4-Oxadiazol-2-ones Undergo Dealkylation upon Nitrogen Insertion to Form 2H-1,2,4-Triazol-3-ones: Synthesis of 1,2,4-Triazol-3-one Hybrids with Triazolothiadiazoles and Triazolothiadiazines

Kattimani, Pramod P. and Kamble, Ravindra R. and Dorababu, A. and Raveendra, K. H. and Kamble, Atulkumar A. and Devarajegowda, H. C. (2017) C5-Alkyl-1,3,4-Oxadiazol-2-ones Undergo Dealkylation upon Nitrogen Insertion to Form 2H-1,2,4-Triazol-3-ones: Synthesis of 1,2,4-Triazol-3-one Hybrids with Triazolothiadiazoles and Triazolothiadiazines. Journal of Heterocyclic Chemistry, 54 (4). pp. 2258-2265. ISSN 1943-5193

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Official URL: https://doi.org/10.1002/jhet.2813

Abstract

The present study emphasizes on the dealklylation of 3-aryl-5-alkyl-2-oxo-Δ4-1,3,4-oxadiazoles when reacted with formamide resulting in the formation of 2-aryl-2H-1,2,4-triazol-3(4H)-ones as major product. Subsequent reactions of 2-aryl-2H-1,2,4-triazol-3(4H)-one gave triazolo3,4-b1,3,4thiadiazoles and triazolo3,4-b1,3,4thiadiazines derivatives incorporated with 1,2,4-triazol-3-one.

Item Type: Article
Subjects: D Physical Science > Physics
Divisions: Yuvaraj college > Physics
Depositing User: C Swapna Library Assistant
Date Deposited: 21 Jun 2019 09:57
Last Modified: 28 Jun 2019 05:40
URI: http://eprints.uni-mysore.ac.in/id/eprint/3604

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