{"title":"Green synthesis and antifungal activities of benzothiazole derivatives containing α-trifluoromethyl tertiary alcohol and coumarin moiety","authors":"Shengfei Jiang, Jianqi Xu, Zhuang Wu, Lulu Wu, Zhenliang Pan, Guoyu Yang, Lijun Shi, Liangxin Fan, Cuilian Xu","doi":"10.1016/j.rechem.2025.102387","DOIUrl":null,"url":null,"abstract":"<div><div>A series of benzothiazole derivatives containing α-trifluoromethyl tertiary alcohol and coumarin moiety were synthesized via the reaction of 2-methylbenzo[<em>d</em>]thiazole and 3-(trifluoroacetyl)coumarin with high yields under catalyst-free and green solvent. The structures of products were validated through <sup>1</sup>H NMR, <sup>13</sup>C NMR, HRMS and X-Ray analysis. Meanwhile, the inhibition activity against five common plant pathogenic fungi: <em>Rhizoctonia solani</em>, <em>Fusarium moniliforme</em>, <em>Phytophthora parasitica</em>, <em>Fusarium graminearum</em> and <em>Fusarium oxysporum</em>, was evaluated in vitro at 200 μg/mL. The results obtained from the bioassay signified that all products possessed significant antifungal effect against <em>Rhizoctonia solani</em> compared to other four fungi.</div></div>","PeriodicalId":420,"journal":{"name":"Results in Chemistry","volume":"16 ","pages":"Article 102387"},"PeriodicalIF":2.5000,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Results in Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211715625003704","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
A series of benzothiazole derivatives containing α-trifluoromethyl tertiary alcohol and coumarin moiety were synthesized via the reaction of 2-methylbenzo[d]thiazole and 3-(trifluoroacetyl)coumarin with high yields under catalyst-free and green solvent. The structures of products were validated through 1H NMR, 13C NMR, HRMS and X-Ray analysis. Meanwhile, the inhibition activity against five common plant pathogenic fungi: Rhizoctonia solani, Fusarium moniliforme, Phytophthora parasitica, Fusarium graminearum and Fusarium oxysporum, was evaluated in vitro at 200 μg/mL. The results obtained from the bioassay signified that all products possessed significant antifungal effect against Rhizoctonia solani compared to other four fungi.