{"title":"1,1,2,2-四苯基二硅烷(TPDS)是一种新型的多样化自由基试剂","authors":"Hideo Togo , Masaaki Sugi , Ken-ichi Toyama","doi":"10.1016/S1387-1609(01)01269-5","DOIUrl":null,"url":null,"abstract":"<div><p>The synthetic utility of 1,1,2,2-tetraphenyldisilane as a new, environmentally benign radical mediator is discussed for the reduction, cyclization, reductive addition to olefins, and alkylation of heteroaromatic bases.</p></div>","PeriodicalId":100305,"journal":{"name":"Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry","volume":"4 7","pages":"Pages 539-546"},"PeriodicalIF":0.0000,"publicationDate":"2001-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1387-1609(01)01269-5","citationCount":"1","resultStr":"{\"title\":\"1,1,2,2-Tetraphenyldisilane (TPDS) as a new diversified radical reagent\",\"authors\":\"Hideo Togo , Masaaki Sugi , Ken-ichi Toyama\",\"doi\":\"10.1016/S1387-1609(01)01269-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The synthetic utility of 1,1,2,2-tetraphenyldisilane as a new, environmentally benign radical mediator is discussed for the reduction, cyclization, reductive addition to olefins, and alkylation of heteroaromatic bases.</p></div>\",\"PeriodicalId\":100305,\"journal\":{\"name\":\"Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry\",\"volume\":\"4 7\",\"pages\":\"Pages 539-546\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2001-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S1387-1609(01)01269-5\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1387160901012695\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1387160901012695","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
1,1,2,2-Tetraphenyldisilane (TPDS) as a new diversified radical reagent
The synthetic utility of 1,1,2,2-tetraphenyldisilane as a new, environmentally benign radical mediator is discussed for the reduction, cyclization, reductive addition to olefins, and alkylation of heteroaromatic bases.
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