{"title":"1,2,4-三唑[3,4-b][1,3,4]恶二唑衍生物的简易合成及对接研究","authors":"Vindhya Hanumanthugari, Asra Banu Syeda, Bhaskar Pittala, Laxminarayana Eppakayala, Mohan Dholvan, Kalyani Sambaru","doi":"10.1134/S0012500824600846","DOIUrl":null,"url":null,"abstract":"<p>A simple and efficient method was developed to synthesize triazole, oxadiazole derivatives. The newly synthesized compounds were confirmed by their IR, <sup>1</sup>H and <sup>13</sup>C NMR, and mass spectral data. Molecular docking studies have been performed for all the derivatives.</p>","PeriodicalId":530,"journal":{"name":"Doklady Chemistry","volume":"515 1-2","pages":"87 - 93"},"PeriodicalIF":1.0000,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Facile Synthesis and Docking Studies of 1,2,4-Triazolo[3,4-b][1,3,4]oxadiazole Derivatives\",\"authors\":\"Vindhya Hanumanthugari, Asra Banu Syeda, Bhaskar Pittala, Laxminarayana Eppakayala, Mohan Dholvan, Kalyani Sambaru\",\"doi\":\"10.1134/S0012500824600846\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A simple and efficient method was developed to synthesize triazole, oxadiazole derivatives. The newly synthesized compounds were confirmed by their IR, <sup>1</sup>H and <sup>13</sup>C NMR, and mass spectral data. Molecular docking studies have been performed for all the derivatives.</p>\",\"PeriodicalId\":530,\"journal\":{\"name\":\"Doklady Chemistry\",\"volume\":\"515 1-2\",\"pages\":\"87 - 93\"},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2025-03-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Doklady Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S0012500824600846\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Doklady Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S0012500824600846","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
A Facile Synthesis and Docking Studies of 1,2,4-Triazolo[3,4-b][1,3,4]oxadiazole Derivatives
A simple and efficient method was developed to synthesize triazole, oxadiazole derivatives. The newly synthesized compounds were confirmed by their IR, 1H and 13C NMR, and mass spectral data. Molecular docking studies have been performed for all the derivatives.
期刊介绍：
Doklady Chemistry is a journal that publishes new research in chemistry and chemical engineering of great significance. Initially the journal was a forum of the Russian Academy of Science and published only best contributions from Russia in the form of short articles. Now the journal welcomes submissions from any country in the English or Russian language. Every manuscript must be recommended by Russian or foreign members of the Russian Academy of Sciences.
京公网安备 11010802042870号
京ICP备2023020795号-1
分享
求助内容：
应助结果提醒方式：
扫码关注我们
