{"title":"超声辐照下 2-巯基苯并咪唑与 α-(三氟甲基)苯乙烯的 (3+3)- 嵌合反应","authors":"Akbar Sohail, Keyume Ablajan, Shahid Ali Khan","doi":"10.1002/ejoc.202401175","DOIUrl":null,"url":null,"abstract":"A rapid and facile sonochemical route for the [3+3] annulation of 2‐mercapto benzimidazoles with α‐(trifluoromethyl)styrene was reported for the synthesis of fluorinated benzo[4,5]imidazo[2,1‑b][1,3]thiazines. The reaction proceeds through the SN2/SNV pathway while the selective SN2 pathway is completely inhibited. The developed method is effective with a wide range of substrates, tolerating diverse functional groups. The pure products are obtained with high yield (up to 92%) directly via recrystallization without column chromatography. Furthermore, applying sonochemical methodology reduces the reaction time and eliminates the need for expensive photocatalysts, ligands or oxidants.","PeriodicalId":167,"journal":{"name":"European Journal of Organic Chemistry","volume":"15 1","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2024-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"(3+3)‐Annulation of 2‐Mercaptobenzimidazoles With α‐(Trifluoromethyl)styrene Under Ultrasonic Irradiation\",\"authors\":\"Akbar Sohail, Keyume Ablajan, Shahid Ali Khan\",\"doi\":\"10.1002/ejoc.202401175\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A rapid and facile sonochemical route for the [3+3] annulation of 2‐mercapto benzimidazoles with α‐(trifluoromethyl)styrene was reported for the synthesis of fluorinated benzo[4,5]imidazo[2,1‑b][1,3]thiazines. The reaction proceeds through the SN2/SNV pathway while the selective SN2 pathway is completely inhibited. The developed method is effective with a wide range of substrates, tolerating diverse functional groups. The pure products are obtained with high yield (up to 92%) directly via recrystallization without column chromatography. Furthermore, applying sonochemical methodology reduces the reaction time and eliminates the need for expensive photocatalysts, ligands or oxidants.\",\"PeriodicalId\":167,\"journal\":{\"name\":\"European Journal of Organic Chemistry\",\"volume\":\"15 1\",\"pages\":\"\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-11-23\",\"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.202401175\",\"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.202401175","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
(3+3)‐Annulation of 2‐Mercaptobenzimidazoles With α‐(Trifluoromethyl)styrene Under Ultrasonic Irradiation
A rapid and facile sonochemical route for the [3+3] annulation of 2‐mercapto benzimidazoles with α‐(trifluoromethyl)styrene was reported for the synthesis of fluorinated benzo[4,5]imidazo[2,1‑b][1,3]thiazines. The reaction proceeds through the SN2/SNV pathway while the selective SN2 pathway is completely inhibited. The developed method is effective with a wide range of substrates, tolerating diverse functional groups. The pure products are obtained with high yield (up to 92%) directly via recrystallization without column chromatography. Furthermore, applying sonochemical methodology reduces the reaction time and eliminates the need for expensive photocatalysts, ligands or oxidants.
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.