{"title":"铜催化的多米诺双-[3 + 2]-环碳酸乙酯与三氟甲基阿兹内酯的环化。","authors":"Chada Raji Reddy,Sana Fatima,Nagender Punna,Balasubramanian Sridhar","doi":"10.1021/acs.orglett.5c03716","DOIUrl":null,"url":null,"abstract":"Herein, we introduce a novel bis-annulation of ethynyl cyclic carbonates with trifluoromethyl azlactones, enabling the assembly of a pyrrolidine-fused lactone containing two quaternary-bridged stereocenters. The reaction proceeds through two [3 + 2]-annulations in a domino mode involving decarboxylative propargylation/lactone formation/aza-annulation reactions with high diastereoselectivity. Interestingly, the scope was extended to ethynyl cyclic carbamates to construct pyrrolidine-fused lactams. This protocol reveals the utility of three reactive sites of both precursors in a single operation for the first time. Further, the scale-up and diverse transformations of the product highlighted its synthetic utility.","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":"68 1","pages":""},"PeriodicalIF":5.0000,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Copper-Catalyzed Domino Bis-[3 + 2]-Annulation of Ethynyl Cyclic Carbonates with Trifluoromethyl Azlactones.\",\"authors\":\"Chada Raji Reddy,Sana Fatima,Nagender Punna,Balasubramanian Sridhar\",\"doi\":\"10.1021/acs.orglett.5c03716\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Herein, we introduce a novel bis-annulation of ethynyl cyclic carbonates with trifluoromethyl azlactones, enabling the assembly of a pyrrolidine-fused lactone containing two quaternary-bridged stereocenters. The reaction proceeds through two [3 + 2]-annulations in a domino mode involving decarboxylative propargylation/lactone formation/aza-annulation reactions with high diastereoselectivity. Interestingly, the scope was extended to ethynyl cyclic carbamates to construct pyrrolidine-fused lactams. This protocol reveals the utility of three reactive sites of both precursors in a single operation for the first time. Further, the scale-up and diverse transformations of the product highlighted its synthetic utility.\",\"PeriodicalId\":54,\"journal\":{\"name\":\"Organic Letters\",\"volume\":\"68 1\",\"pages\":\"\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-09-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.orglett.5c03716\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Letters","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.orglett.5c03716","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Copper-Catalyzed Domino Bis-[3 + 2]-Annulation of Ethynyl Cyclic Carbonates with Trifluoromethyl Azlactones.
Herein, we introduce a novel bis-annulation of ethynyl cyclic carbonates with trifluoromethyl azlactones, enabling the assembly of a pyrrolidine-fused lactone containing two quaternary-bridged stereocenters. The reaction proceeds through two [3 + 2]-annulations in a domino mode involving decarboxylative propargylation/lactone formation/aza-annulation reactions with high diastereoselectivity. Interestingly, the scope was extended to ethynyl cyclic carbamates to construct pyrrolidine-fused lactams. This protocol reveals the utility of three reactive sites of both precursors in a single operation for the first time. Further, the scale-up and diverse transformations of the product highlighted its synthetic utility.
期刊介绍:
Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.