{"title":"有机碘催化分子内 C-N 键氧化偶联合成 3-单取代羰基吲哚","authors":"Yang Wang, Jiang-Ning Yu, Yue Wang, Ji-Chen Yin","doi":"10.1002/ejoc.202400822","DOIUrl":null,"url":null,"abstract":"An efficient organoiodine-catalysed intramolecular direct C–N bond oxidative coupling reaction is presented. Structurally diverse 3-(mono)substituted oxindoles were rapidly obtained in a complex oxidative system in up to 87% yield. Various N-alkoxy-2-phenylpropanamides were well-tolerated. This study showed that the electronic effects on the aromatic ring of reactants have a crucial effect on the selectivity (C−N/C−O) of cyclisation products. In addition, gram-scale synthesis and late-stage modification of 3-(mono)substituted oxindole derivatives revealed the practical application of this transformation.","PeriodicalId":167,"journal":{"name":"European Journal of Organic Chemistry","volume":"17 1","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2024-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Organoiodine Catalysed Intramolecular C−N bond Oxidative Coupling for the Synthesis of 3-Monosubstituted Oxindoles\",\"authors\":\"Yang Wang, Jiang-Ning Yu, Yue Wang, Ji-Chen Yin\",\"doi\":\"10.1002/ejoc.202400822\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An efficient organoiodine-catalysed intramolecular direct C–N bond oxidative coupling reaction is presented. Structurally diverse 3-(mono)substituted oxindoles were rapidly obtained in a complex oxidative system in up to 87% yield. Various N-alkoxy-2-phenylpropanamides were well-tolerated. This study showed that the electronic effects on the aromatic ring of reactants have a crucial effect on the selectivity (C−N/C−O) of cyclisation products. In addition, gram-scale synthesis and late-stage modification of 3-(mono)substituted oxindole derivatives revealed the practical application of this transformation.\",\"PeriodicalId\":167,\"journal\":{\"name\":\"European Journal of Organic Chemistry\",\"volume\":\"17 1\",\"pages\":\"\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-10-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/ejoc.202400822\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/ejoc.202400822","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Organoiodine Catalysed Intramolecular C−N bond Oxidative Coupling for the Synthesis of 3-Monosubstituted Oxindoles
An efficient organoiodine-catalysed intramolecular direct C–N bond oxidative coupling reaction is presented. Structurally diverse 3-(mono)substituted oxindoles were rapidly obtained in a complex oxidative system in up to 87% yield. Various N-alkoxy-2-phenylpropanamides were well-tolerated. This study showed that the electronic effects on the aromatic ring of reactants have a crucial effect on the selectivity (C−N/C−O) of cyclisation products. In addition, gram-scale synthesis and late-stage modification of 3-(mono)substituted oxindole derivatives revealed the practical application of this transformation.
期刊介绍:
The European Journal of Organic Chemistry (2019 ISI Impact Factor 2.889) publishes Full Papers, Communications, and Minireviews from the entire spectrum of synthetic organic, bioorganic and physical-organic chemistry. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies.
The following journals have been merged to form two leading journals, the European Journal of Organic Chemistry and the European Journal of Inorganic Chemistry:
Liebigs Annalen
Bulletin des Sociétés Chimiques Belges
Bulletin de la Société Chimique de France
Gazzetta Chimica Italiana
Recueil des Travaux Chimiques des Pays-Bas
Anales de Química
Chimika Chronika
Revista Portuguesa de Química
ACH—Models in Chemistry
Polish Journal of Chemistry.