{"title":"醛和酮与四羟基二硼酸在水中的转移氢化反应","authors":"Kaili Zhang, S. Okumura, Yasuhiro Uozumi","doi":"10.1093/chemle/upae082","DOIUrl":null,"url":null,"abstract":"\n We have developed a transfer hydrogenation of aldehydes and ketones with B2(OH)4 as a reductant and amphiphilic resin-dispersed palladium nanoparticles as a catalyst system in an aqueous medium, where water also serves as a hydrogen donor. A variety of aldehydes and ketones, including aliphatic carbonyl compounds, reacted to give the corresponding primary and secondary alcohols, respectively. The catalyst was recovered by filtration and reused nine times without a significant loss of its catalytic activity.","PeriodicalId":9862,"journal":{"name":"Chemistry Letters","volume":null,"pages":null},"PeriodicalIF":1.4000,"publicationDate":"2024-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Transfer-Hydrogenation of Aldehydes and Ketones with Tetrahydroxydiboran in Water\",\"authors\":\"Kaili Zhang, S. Okumura, Yasuhiro Uozumi\",\"doi\":\"10.1093/chemle/upae082\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n We have developed a transfer hydrogenation of aldehydes and ketones with B2(OH)4 as a reductant and amphiphilic resin-dispersed palladium nanoparticles as a catalyst system in an aqueous medium, where water also serves as a hydrogen donor. A variety of aldehydes and ketones, including aliphatic carbonyl compounds, reacted to give the corresponding primary and secondary alcohols, respectively. The catalyst was recovered by filtration and reused nine times without a significant loss of its catalytic activity.\",\"PeriodicalId\":9862,\"journal\":{\"name\":\"Chemistry Letters\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2024-05-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1093/chemle/upae082\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry Letters","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1093/chemle/upae082","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Transfer-Hydrogenation of Aldehydes and Ketones with Tetrahydroxydiboran in Water
We have developed a transfer hydrogenation of aldehydes and ketones with B2(OH)4 as a reductant and amphiphilic resin-dispersed palladium nanoparticles as a catalyst system in an aqueous medium, where water also serves as a hydrogen donor. A variety of aldehydes and ketones, including aliphatic carbonyl compounds, reacted to give the corresponding primary and secondary alcohols, respectively. The catalyst was recovered by filtration and reused nine times without a significant loss of its catalytic activity.