{"title":"1-安替吡基-4-芳基-5-甲氧基羰基- 1h -吡咯-2,3-二酮与n-取代和n-未取代的3-氨基-5,5-二甲基环己基-2-烯-1的反应","authors":"V. A. Lyadov, E. S. Denislamova, A. N. Maslivets","doi":"10.1134/S1070428024603996","DOIUrl":null,"url":null,"abstract":"<p>Nucleophilic transformations of <i>N</i>-antipyryl-substituted 1<i>H</i>-pyrrole-2,3-diones by the action of enamines derived from dimedone as 1,3-C,N-binucleophiles afforded 1′-antipyryl-3′-aroyl-4′-hydroxy-6,6-dimethyl-6,7-dihydrospiro[indole-3,2′-pyrrole]-2,4,5′(1<i>H</i>,1′<i>H</i>,5<i>H</i>)-triones and 1′-antipyryl-1-aryl-3′-aroyl-4′-hydroxy-6,6-dimethyl-6,7-dihydrospiro[indole-3,2′-pyrrole]-2,4,5′(1<i>H</i>,1′<i>H</i>,5<i>H</i>)-triones.</p>","PeriodicalId":766,"journal":{"name":"Russian Journal of Organic Chemistry","volume":"61 3","pages":"374 - 377"},"PeriodicalIF":0.8000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reaction of 1-Antipyryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones with N-Substituted and N-Unsubstituted 3-Amino-5,5-dimethylcyclohex-2-en-1-ones\",\"authors\":\"V. A. Lyadov, E. S. Denislamova, A. N. Maslivets\",\"doi\":\"10.1134/S1070428024603996\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Nucleophilic transformations of <i>N</i>-antipyryl-substituted 1<i>H</i>-pyrrole-2,3-diones by the action of enamines derived from dimedone as 1,3-C,N-binucleophiles afforded 1′-antipyryl-3′-aroyl-4′-hydroxy-6,6-dimethyl-6,7-dihydrospiro[indole-3,2′-pyrrole]-2,4,5′(1<i>H</i>,1′<i>H</i>,5<i>H</i>)-triones and 1′-antipyryl-1-aryl-3′-aroyl-4′-hydroxy-6,6-dimethyl-6,7-dihydrospiro[indole-3,2′-pyrrole]-2,4,5′(1<i>H</i>,1′<i>H</i>,5<i>H</i>)-triones.</p>\",\"PeriodicalId\":766,\"journal\":{\"name\":\"Russian Journal of Organic Chemistry\",\"volume\":\"61 3\",\"pages\":\"374 - 377\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2025-05-07\",\"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/S1070428024603996\",\"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/S1070428024603996","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Reaction of 1-Antipyryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones with N-Substituted and N-Unsubstituted 3-Amino-5,5-dimethylcyclohex-2-en-1-ones
Nucleophilic transformations of N-antipyryl-substituted 1H-pyrrole-2,3-diones by the action of enamines derived from dimedone as 1,3-C,N-binucleophiles afforded 1′-antipyryl-3′-aroyl-4′-hydroxy-6,6-dimethyl-6,7-dihydrospiro[indole-3,2′-pyrrole]-2,4,5′(1H,1′H,5H)-triones and 1′-antipyryl-1-aryl-3′-aroyl-4′-hydroxy-6,6-dimethyl-6,7-dihydrospiro[indole-3,2′-pyrrole]-2,4,5′(1H,1′H,5H)-triones.
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.