{"title":"用无膦钌二胺催化剂催化四氢γ卡泊啉衍生物的不对称加氢反应","authors":"Zi‐Qi Yi, Fei Chen, Yan‐Mei He, Qing‐Hua Fan","doi":"10.1002/adsc.70029","DOIUrl":null,"url":null,"abstract":"A highly efficient asymmetric hydrogenation of tetrahydro‐<jats:italic>γ</jats:italic>‐carboline derivatives catalyzed by phosphine‐free ruthenium diamine catalysts has been developed, providing the corresponding <jats:italic>cis</jats:italic>‐hexahydro‐<jats:italic>γ</jats:italic>‐carbolines with excellent enantioselectivities and diastereoselectivities (up to 99% ee and >20:1 dr). Furthermore, this catalytic protocol is applicable to the gram‐scale synthesis of cardioprotective drug (‐)‐stobadin.","PeriodicalId":118,"journal":{"name":"Advanced Synthesis & Catalysis","volume":"4 1","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Asymmetric Hydrogenation of Tetrahydro‐γ‐Carboline Derivatives with Phosphine‐Free Ruthenium Diamine Catalysts\",\"authors\":\"Zi‐Qi Yi, Fei Chen, Yan‐Mei He, Qing‐Hua Fan\",\"doi\":\"10.1002/adsc.70029\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A highly efficient asymmetric hydrogenation of tetrahydro‐<jats:italic>γ</jats:italic>‐carboline derivatives catalyzed by phosphine‐free ruthenium diamine catalysts has been developed, providing the corresponding <jats:italic>cis</jats:italic>‐hexahydro‐<jats:italic>γ</jats:italic>‐carbolines with excellent enantioselectivities and diastereoselectivities (up to 99% ee and >20:1 dr). Furthermore, this catalytic protocol is applicable to the gram‐scale synthesis of cardioprotective drug (‐)‐stobadin.\",\"PeriodicalId\":118,\"journal\":{\"name\":\"Advanced Synthesis & Catalysis\",\"volume\":\"4 1\",\"pages\":\"\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-07-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Synthesis & Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/adsc.70029\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Synthesis & Catalysis","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/adsc.70029","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Asymmetric Hydrogenation of Tetrahydro‐γ‐Carboline Derivatives with Phosphine‐Free Ruthenium Diamine Catalysts
A highly efficient asymmetric hydrogenation of tetrahydro‐γ‐carboline derivatives catalyzed by phosphine‐free ruthenium diamine catalysts has been developed, providing the corresponding cis‐hexahydro‐γ‐carbolines with excellent enantioselectivities and diastereoselectivities (up to 99% ee and >20:1 dr). Furthermore, this catalytic protocol is applicable to the gram‐scale synthesis of cardioprotective drug (‐)‐stobadin.
期刊介绍:
Advanced Synthesis & Catalysis (ASC) is the leading primary journal in organic, organometallic, and applied chemistry.
The high impact of ASC can be attributed to the unique focus of the journal, which publishes exciting new results from academic and industrial labs on efficient, practical, and environmentally friendly organic synthesis. While homogeneous, heterogeneous, organic, and enzyme catalysis are key technologies to achieve green synthesis, significant contributions to the same goal by synthesis design, reaction techniques, flow chemistry, and continuous processing, multiphase catalysis, green solvents, catalyst immobilization, and recycling, separation science, and process development are also featured in ASC. The Aims and Scope can be found in the Notice to Authors or on the first page of the table of contents in every issue.