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{"title":"钯催化合成(E)-5-(3-氨基烯丙基)-尿苷-5′- o -三磷酸酯","authors":"Muthian Shanmugasundaram, Annamalai Senthilvelan, Anilkumar R. Kore","doi":"10.1002/cpnc.42","DOIUrl":null,"url":null,"abstract":"<p>This unit describes a simple, reliable, and efficient chemical method for the synthesis of 5-(3-aminoallyl)-2′-deoxyuridine-5′-<i>O</i>-triphosphate (AA-dUTP) and 5-(3-aminoallyl)-uridine-5′-<i>O</i>-triphosphate (AA-UTP), starting from the corresponding nucleoside triphosphate. The presented strategy involves regioselective iodination of nucleoside triphosphate using <i>N</i>-iodosuccinimide followed by the palladium-catalyzed Heck coupling with allylamine to provide the corresponding (<i>E</i>)-5-aminoallyl-uridine-5′-<i>O</i>-triphosphate in good yields. It is noteworthy that the protocol not only provides a high-purity product but also eliminates the use of toxic mercuric reagents. © 2017 by John Wiley & Sons, Inc.</p>","PeriodicalId":10966,"journal":{"name":"Current Protocols in Nucleic Acid Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2018-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpnc.42","citationCount":"1","resultStr":"{\"title\":\"Palladium-Catalyzed Synthesis of (E)-5-(3-Aminoallyl)-Uridine-5′-O-Triphosphates\",\"authors\":\"Muthian Shanmugasundaram, Annamalai Senthilvelan, Anilkumar R. Kore\",\"doi\":\"10.1002/cpnc.42\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>This unit describes a simple, reliable, and efficient chemical method for the synthesis of 5-(3-aminoallyl)-2′-deoxyuridine-5′-<i>O</i>-triphosphate (AA-dUTP) and 5-(3-aminoallyl)-uridine-5′-<i>O</i>-triphosphate (AA-UTP), starting from the corresponding nucleoside triphosphate. The presented strategy involves regioselective iodination of nucleoside triphosphate using <i>N</i>-iodosuccinimide followed by the palladium-catalyzed Heck coupling with allylamine to provide the corresponding (<i>E</i>)-5-aminoallyl-uridine-5′-<i>O</i>-triphosphate in good yields. It is noteworthy that the protocol not only provides a high-purity product but also eliminates the use of toxic mercuric reagents. © 2017 by John Wiley & Sons, Inc.</p>\",\"PeriodicalId\":10966,\"journal\":{\"name\":\"Current Protocols in Nucleic Acid Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-02-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/cpnc.42\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Protocols in Nucleic Acid Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cpnc.42\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Chemistry\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Nucleic Acid Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpnc.42","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Chemistry","Score":null,"Total":0}
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