{"title":"HFIP/BF3·Et2O协同催化实现香豆素分子内炔环化。","authors":"Yu Zhao, , , Yu Cheng, , , Quanye Liu, , , Mengyi Li, , , Wei Li*, , and , Di Wu*, ","doi":"10.1021/acs.joc.5c01199","DOIUrl":null,"url":null,"abstract":"<p >We have successfully developed a novel synergistic catalytic system employing hexafluoroisopropanol (HFIP)/BF<sub>3</sub>·Et<sub>2</sub>O for intramolecular alkyne cyclization, which enables efficient construction of coumarin frameworks. This metal-free protocol features mild reaction conditions and exceptional substrate generality. The methodology has been directly applied to the synthesis of pharmacologically important natural products and drug molecules. Systematic mechanistic investigations have uncovered the cooperative catalytic mechanism of HFIP in this transformation, providing new fundamental principles for reaction design.</p>","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"90 40","pages":"14304–14311"},"PeriodicalIF":3.6000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"HFIP/BF3·Et2O Synergistic Catalysis Enables Intramolecular Alkyne Cyclization to Coumarins\",\"authors\":\"Yu Zhao, , , Yu Cheng, , , Quanye Liu, , , Mengyi Li, , , Wei Li*, , and , Di Wu*, \",\"doi\":\"10.1021/acs.joc.5c01199\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >We have successfully developed a novel synergistic catalytic system employing hexafluoroisopropanol (HFIP)/BF<sub>3</sub>·Et<sub>2</sub>O for intramolecular alkyne cyclization, which enables efficient construction of coumarin frameworks. This metal-free protocol features mild reaction conditions and exceptional substrate generality. The methodology has been directly applied to the synthesis of pharmacologically important natural products and drug molecules. Systematic mechanistic investigations have uncovered the cooperative catalytic mechanism of HFIP in this transformation, providing new fundamental principles for reaction design.</p>\",\"PeriodicalId\":57,\"journal\":{\"name\":\"Journal of Organic Chemistry\",\"volume\":\"90 40\",\"pages\":\"14304–14311\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-10-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Organic Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.joc.5c01199\",\"RegionNum\":2,\"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":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.joc.5c01199","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
HFIP/BF3·Et2O Synergistic Catalysis Enables Intramolecular Alkyne Cyclization to Coumarins
We have successfully developed a novel synergistic catalytic system employing hexafluoroisopropanol (HFIP)/BF3·Et2O for intramolecular alkyne cyclization, which enables efficient construction of coumarin frameworks. This metal-free protocol features mild reaction conditions and exceptional substrate generality. The methodology has been directly applied to the synthesis of pharmacologically important natural products and drug molecules. Systematic mechanistic investigations have uncovered the cooperative catalytic mechanism of HFIP in this transformation, providing new fundamental principles for reaction design.
期刊介绍:
Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.