Literature DB >> 29275536

Palladium-Catalyzed Synthesis of (E)-5-(3-Aminoallyl)-Uridine-5'-O-Triphosphates.

Muthian Shanmugasundaram1, Annamalai Senthilvelan1, Anilkumar R Kore1.   

Abstract

This unit describes a simple, reliable, and efficient chemical method for the synthesis of 5-(3-aminoallyl)-2'-deoxyuridine-5'-O-triphosphate (AA-dUTP) and 5-(3-aminoallyl)-uridine-5'-O-triphosphate (AA-UTP), starting from the corresponding nucleoside triphosphate. The presented strategy involves regioselective iodination of nucleoside triphosphate using N-iodosuccinimide followed by the palladium-catalyzed Heck coupling with allylamine to provide the corresponding (E)-5-aminoallyl-uridine-5'-O-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.
Copyright © 2017 John Wiley & Sons, Inc.

Entities:  

Keywords:  5-(3-aminoallyl)-2′-deoxyuridine-5′-O-triphosphate (AA-dUTP); 5-(3-aminoallyl)-2′-uridine-5′-O-triphosphate (AA-UTP); cDNA microarrays; gene expression; labeling; reverse transcription

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Year:  2017        PMID: 29275536     DOI: 10.1002/cpnc.42

Source DB:  PubMed          Journal:  Curr Protoc Nucleic Acid Chem        ISSN: 1934-9270


  1 in total

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Authors:  Muthian Shanmugasundaram; Annamalai Senthilvelan; Anilkumar R Kore
Journal:  Chem Rec       Date:  2022-04-14       Impact factor: 6.935

  1 in total

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