{"title":"碱基促进炔烯酮催化区域选择性和非对映选择性合成三取代和四取代均烯基膦氧化物","authors":"Shaochan Zhou , Haotian Zou , Xianqiang Huang , Jialin Qi , Zhenghu Xu","doi":"10.1039/d5ob00446b","DOIUrl":null,"url":null,"abstract":"<div><div>A novel base-promoted method for hydrophosphinylation of alkynyl enones with secondary phosphine oxides has been developed. Using inexpensive and commercially available potassium carbonate, a variety of functionalized tri-substituted allene products were synthesized with exclusive regio- and diastereoselectivity under mild conditions. Furthermore, a one-pot, two-step, three-component tandem hydrophosphinylation/Heck reaction efficiently produced tetra-substituted homoallenyl phosphine oxides in excellent yields, demonstrating a relatively broad substrate scope.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"23 19","pages":"Pages 4718-4724"},"PeriodicalIF":2.7000,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Base-promoted regio- and diastereoselective synthesis of tri- and tetra-substituted homoallenyl phosphine oxides via alkynyl enones†\",\"authors\":\"Shaochan Zhou , Haotian Zou , Xianqiang Huang , Jialin Qi , Zhenghu Xu\",\"doi\":\"10.1039/d5ob00446b\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A novel base-promoted method for hydrophosphinylation of alkynyl enones with secondary phosphine oxides has been developed. Using inexpensive and commercially available potassium carbonate, a variety of functionalized tri-substituted allene products were synthesized with exclusive regio- and diastereoselectivity under mild conditions. Furthermore, a one-pot, two-step, three-component tandem hydrophosphinylation/Heck reaction efficiently produced tetra-substituted homoallenyl phosphine oxides in excellent yields, demonstrating a relatively broad substrate scope.</div></div>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\"23 19\",\"pages\":\"Pages 4718-4724\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-04-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S147705202500299X\",\"RegionNum\":3,\"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 & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S147705202500299X","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Base-promoted regio- and diastereoselective synthesis of tri- and tetra-substituted homoallenyl phosphine oxides via alkynyl enones†
A novel base-promoted method for hydrophosphinylation of alkynyl enones with secondary phosphine oxides has been developed. Using inexpensive and commercially available potassium carbonate, a variety of functionalized tri-substituted allene products were synthesized with exclusive regio- and diastereoselectivity under mild conditions. Furthermore, a one-pot, two-step, three-component tandem hydrophosphinylation/Heck reaction efficiently produced tetra-substituted homoallenyl phosphine oxides in excellent yields, demonstrating a relatively broad substrate scope.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.