Xinpeng Fu , Hanxiao Yu , Haoyang Gao , Yuhao Dai , He Yang , Wenjun Tang
{"title":"酮类不对称转移加氢的手性二茂铁系钌二胺催化剂","authors":"Xinpeng Fu , Hanxiao Yu , Haoyang Gao , Yuhao Dai , He Yang , Wenjun Tang","doi":"10.1039/d5qo00077g","DOIUrl":null,"url":null,"abstract":"<div><div>A chiral ferrocene-tethered ruthenium diamine catalyst has been developed for asymmetric transfer hydrogenation of ketones, enabling asymmetric reduction of a wide range of ketones including aryl alkyl ketones and cyclic dialkyl ketones with excellent reactivities and enantioselectivities. Efficient dynamic kinetic resolution (DKR) of racemic α-substituted cyclic ketones was established, affording a series of cyclic chiral alcohols with two contiguous stereocenters in high yields and excellent enantio- and diastereoselectivity levels. The chiral ATH Ru catalyst was found to offer practicality, with a TON of up to 4000.</div></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"12 9","pages":"Pages 2957-2962"},"PeriodicalIF":0.0000,"publicationDate":"2025-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A chiral ferrocene-tethered ruthenium diamine catalyst for asymmetric transfer hydrogenation of ketones†\",\"authors\":\"Xinpeng Fu , Hanxiao Yu , Haoyang Gao , Yuhao Dai , He Yang , Wenjun Tang\",\"doi\":\"10.1039/d5qo00077g\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A chiral ferrocene-tethered ruthenium diamine catalyst has been developed for asymmetric transfer hydrogenation of ketones, enabling asymmetric reduction of a wide range of ketones including aryl alkyl ketones and cyclic dialkyl ketones with excellent reactivities and enantioselectivities. Efficient dynamic kinetic resolution (DKR) of racemic α-substituted cyclic ketones was established, affording a series of cyclic chiral alcohols with two contiguous stereocenters in high yields and excellent enantio- and diastereoselectivity levels. The chiral ATH Ru catalyst was found to offer practicality, with a TON of up to 4000.</div></div>\",\"PeriodicalId\":94379,\"journal\":{\"name\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"volume\":\"12 9\",\"pages\":\"Pages 2957-2962\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-02-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2052412925001342\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/3/5 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic chemistry frontiers : an international journal of organic chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2052412925001342","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/5 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
A chiral ferrocene-tethered ruthenium diamine catalyst for asymmetric transfer hydrogenation of ketones†
A chiral ferrocene-tethered ruthenium diamine catalyst has been developed for asymmetric transfer hydrogenation of ketones, enabling asymmetric reduction of a wide range of ketones including aryl alkyl ketones and cyclic dialkyl ketones with excellent reactivities and enantioselectivities. Efficient dynamic kinetic resolution (DKR) of racemic α-substituted cyclic ketones was established, affording a series of cyclic chiral alcohols with two contiguous stereocenters in high yields and excellent enantio- and diastereoselectivity levels. The chiral ATH Ru catalyst was found to offer practicality, with a TON of up to 4000.