{"title":"α-(1H-苯并三唑-1-基)硝基酮与格氏试剂的偶联：获得酮基丙酮","authors":"Khalid Widyan","doi":"10.1134/S1070428024050178","DOIUrl":null,"url":null,"abstract":"<p>A new procedure for the synthesis of novel ketonitrones has been developed. The procedure involves the coupling of Grignard reagents with the easily accessible and stable <i>N</i>-substituted α-(1<i>H</i>-benzotriazol-1-yl) nitrones in the presence of catalytic amounts of zinc bromide.</p>","PeriodicalId":766,"journal":{"name":"Russian Journal of Organic Chemistry","volume":null,"pages":null},"PeriodicalIF":0.8000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Coupling of α-(1H-Benzotriazol-1-yl) Nitrones with Grignard Reagents: Access to Ketonitrones\",\"authors\":\"Khalid Widyan\",\"doi\":\"10.1134/S1070428024050178\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A new procedure for the synthesis of novel ketonitrones has been developed. The procedure involves the coupling of Grignard reagents with the easily accessible and stable <i>N</i>-substituted α-(1<i>H</i>-benzotriazol-1-yl) nitrones in the presence of catalytic amounts of zinc bromide.</p>\",\"PeriodicalId\":766,\"journal\":{\"name\":\"Russian Journal of Organic Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2024-07-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Russian Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S1070428024050178\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1070428024050178","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Coupling of α-(1H-Benzotriazol-1-yl) Nitrones with Grignard Reagents: Access to Ketonitrones
A new procedure for the synthesis of novel ketonitrones has been developed. The procedure involves the coupling of Grignard reagents with the easily accessible and stable N-substituted α-(1H-benzotriazol-1-yl) nitrones in the presence of catalytic amounts of zinc bromide.
期刊介绍：
Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.
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