Shijie Zhu, Jiaojiao Lei, Shengwen Yang, Zhifei Zhao, Ning Liu, Shi-Wu Li
{"title":"fecl3催化氮杂七烯与双环[1.1.0]丁烷的分子间形式[8π+2σ]环加成合成环庚三烯- 2-氮杂环[3.1.1]庚烷","authors":"Shijie Zhu, Jiaojiao Lei, Shengwen Yang, Zhifei Zhao, Ning Liu, Shi-Wu Li","doi":"10.1021/acs.orglett.5c00489","DOIUrl":null,"url":null,"abstract":"Higher-order cycloadditions are a simple and effective strategy for constructing significant medium-sized architectures. Azaheptafulvenes reacting with readily accessible bicyclo[1.1.0]butanes (BCBs) through FeCl<sub>3</sub>-promoted intermolecular formal [8π+2σ] cycloaddition reactions to access cycloheptatriene-fused 2-azabicyclo[3.1.1]heptanes have been developed. This new reaction tolerated a wide range of azaheptafulvenes and BCBs. Furthermore, the amplification experiment and synthetic transformations of the adducts, including modifications of marketed drugs, further highlighted their practicalities. Control experiments and DFT calculations suggest that the diastereoselective [8π+2σ] product formation may involve a stepwise pathway.","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":"108 1","pages":""},"PeriodicalIF":4.9000,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"FeCl3-Catalyzed Intermolecular Formal [8π+2σ] Cycloaddition of Azaheptafulvene with Bicyclo[1.1.0]butanes for the Synthesis of Cycloheptatriene-Fused 2-Azabicyclo[3.1.1]heptanes\",\"authors\":\"Shijie Zhu, Jiaojiao Lei, Shengwen Yang, Zhifei Zhao, Ning Liu, Shi-Wu Li\",\"doi\":\"10.1021/acs.orglett.5c00489\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Higher-order cycloadditions are a simple and effective strategy for constructing significant medium-sized architectures. Azaheptafulvenes reacting with readily accessible bicyclo[1.1.0]butanes (BCBs) through FeCl<sub>3</sub>-promoted intermolecular formal [8π+2σ] cycloaddition reactions to access cycloheptatriene-fused 2-azabicyclo[3.1.1]heptanes have been developed. This new reaction tolerated a wide range of azaheptafulvenes and BCBs. Furthermore, the amplification experiment and synthetic transformations of the adducts, including modifications of marketed drugs, further highlighted their practicalities. Control experiments and DFT calculations suggest that the diastereoselective [8π+2σ] product formation may involve a stepwise pathway.\",\"PeriodicalId\":54,\"journal\":{\"name\":\"Organic Letters\",\"volume\":\"108 1\",\"pages\":\"\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2025-04-08\",\"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.5c00489\",\"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.5c00489","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
FeCl3-Catalyzed Intermolecular Formal [8π+2σ] Cycloaddition of Azaheptafulvene with Bicyclo[1.1.0]butanes for the Synthesis of Cycloheptatriene-Fused 2-Azabicyclo[3.1.1]heptanes
Higher-order cycloadditions are a simple and effective strategy for constructing significant medium-sized architectures. Azaheptafulvenes reacting with readily accessible bicyclo[1.1.0]butanes (BCBs) through FeCl3-promoted intermolecular formal [8π+2σ] cycloaddition reactions to access cycloheptatriene-fused 2-azabicyclo[3.1.1]heptanes have been developed. This new reaction tolerated a wide range of azaheptafulvenes and BCBs. Furthermore, the amplification experiment and synthetic transformations of the adducts, including modifications of marketed drugs, further highlighted their practicalities. Control experiments and DFT calculations suggest that the diastereoselective [8π+2σ] product formation may involve a stepwise pathway.
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.