Tiantian Yin , Shiyuan Sui , Shuqi Li , Junbiao Chang , Dachang Bai
{"title":"镍催化乙烯基氯硅烷与轴向手性双芳基亲电体的立体特异性还原交叉偶联反应","authors":"Tiantian Yin , Shiyuan Sui , Shuqi Li , Junbiao Chang , Dachang Bai","doi":"10.1039/d4cc04293j","DOIUrl":null,"url":null,"abstract":"<div><div>Enantioenriched organosilanes are important chiral molecules in materials science and organic synthesis. The synthesis of axially chiral organosilanes is particularly significant in terms of applications. Herein, we report a Ni-catalyzed reductive cross-electrophile coupling of vinyl chlorosilanes with sterically hindered chiral biaryl electrophiles for the synthesis of atropisomeric biaryl organosilanes. Various enantioenriched axially chiral vinylsilanes are accessible in high efficiency under mild conditions. The synthetic transformations and applications of new chiral silicon-containing alkene ligands are demonstrated.</div></div>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"60 96","pages":"Pages 14204-14207"},"PeriodicalIF":4.2000,"publicationDate":"2024-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nickel-catalyzed stereospecific reductive cross-coupling of vinyl chlorosilanes with axially chiral biaryl electrophiles†\",\"authors\":\"Tiantian Yin , Shiyuan Sui , Shuqi Li , Junbiao Chang , Dachang Bai\",\"doi\":\"10.1039/d4cc04293j\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Enantioenriched organosilanes are important chiral molecules in materials science and organic synthesis. The synthesis of axially chiral organosilanes is particularly significant in terms of applications. Herein, we report a Ni-catalyzed reductive cross-electrophile coupling of vinyl chlorosilanes with sterically hindered chiral biaryl electrophiles for the synthesis of atropisomeric biaryl organosilanes. Various enantioenriched axially chiral vinylsilanes are accessible in high efficiency under mild conditions. The synthetic transformations and applications of new chiral silicon-containing alkene ligands are demonstrated.</div></div>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"60 96\",\"pages\":\"Pages 14204-14207\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2024-11-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1359734524023620\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1359734524023620","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Nickel-catalyzed stereospecific reductive cross-coupling of vinyl chlorosilanes with axially chiral biaryl electrophiles†
Enantioenriched organosilanes are important chiral molecules in materials science and organic synthesis. The synthesis of axially chiral organosilanes is particularly significant in terms of applications. Herein, we report a Ni-catalyzed reductive cross-electrophile coupling of vinyl chlorosilanes with sterically hindered chiral biaryl electrophiles for the synthesis of atropisomeric biaryl organosilanes. Various enantioenriched axially chiral vinylsilanes are accessible in high efficiency under mild conditions. The synthetic transformations and applications of new chiral silicon-containing alkene ligands are demonstrated.
期刊介绍:
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