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
Full text not available from this repository. (Request a copy)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 |
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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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