| Literature DB >> 29275536 |
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.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
Mesh:
Substances:
Year: 2017 PMID: 29275536 DOI: 10.1002/cpnc.42
Source DB: PubMed Journal: Curr Protoc Nucleic Acid Chem ISSN: 1934-9270