{"title":"钯催化乙醇为氢供体的末端炔转移加氢反应","authors":"Jie Hui, Feng Wang","doi":"10.1177/17475198221145838","DOIUrl":null,"url":null,"abstract":"A ligand-promoted, palladium-catalyzed transfer hydrogenation of terminal alkynes using ethanol as the hydrogen donor is developed. The chemical selectivity control is achieved based on ligand regulation. The use of triethanolamine and tetrahydrofuran at 80 °C under N2 is found to be critical for the transfer hydrogenation of terminal alkynes. The general applicability of this procedure is highlighted by the synthesis of 27 terminal alkenes in moderate to good yields.","PeriodicalId":15318,"journal":{"name":"Journal of Chemical Research-s","volume":"234 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Palladium-catalyzed transfer hydrogenation of terminal alkynes using ethanol as the hydrogen donor\",\"authors\":\"Jie Hui, Feng Wang\",\"doi\":\"10.1177/17475198221145838\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A ligand-promoted, palladium-catalyzed transfer hydrogenation of terminal alkynes using ethanol as the hydrogen donor is developed. The chemical selectivity control is achieved based on ligand regulation. The use of triethanolamine and tetrahydrofuran at 80 °C under N2 is found to be critical for the transfer hydrogenation of terminal alkynes. The general applicability of this procedure is highlighted by the synthesis of 27 terminal alkenes in moderate to good yields.\",\"PeriodicalId\":15318,\"journal\":{\"name\":\"Journal of Chemical Research-s\",\"volume\":\"234 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Research-s\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1177/17475198221145838\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Research-s","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/17475198221145838","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Palladium-catalyzed transfer hydrogenation of terminal alkynes using ethanol as the hydrogen donor
A ligand-promoted, palladium-catalyzed transfer hydrogenation of terminal alkynes using ethanol as the hydrogen donor is developed. The chemical selectivity control is achieved based on ligand regulation. The use of triethanolamine and tetrahydrofuran at 80 °C under N2 is found to be critical for the transfer hydrogenation of terminal alkynes. The general applicability of this procedure is highlighted by the synthesis of 27 terminal alkenes in moderate to good yields.
期刊介绍:
The Journal of Chemical Research is a peer reviewed journal that publishes full-length review and research papers in all branches of experimental chemistry. The journal fills a niche by also publishing short papers, a format which favours particular types of work, e.g. the scope of new reagents or methodology, and the elucidation of the structure of novel compounds. Though welcome, short papers should not result in fragmentation of publication, they should describe a completed piece of work. The Journal is not intended as a vehicle for preliminary publications. The work must meet all the normal criteria for acceptance as regards scientific standards. Papers that contain extensive biological results or material relating to other areas of science may be diverted to more appropriate specialist journals. Areas of coverage include: Organic Chemistry; Inorganic Chemistry; Materials Chemistry; Crystallography; Computational Chemistry.