Shanmugasundaram Muthian, Senthilvelan Annamalai, Kore Anilkumar R
Life Sciences Solutions Group, Thermo Fisher Scientific, Austin, Texas.
Curr Protoc Nucleic Acid Chem. 2017 Dec 24;71:13.18.1-13.18.10. doi: 10.1002/cpnc.42.
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.
本单元描述了一种从相应的核苷三磷酸开始,合成5-(3-氨基烯丙基)-2'-脱氧尿苷-5'-O-三磷酸(AA-dUTP)和5-(3-氨基烯丙基)-尿苷-5'-O-三磷酸(AA-UTP)的简单、可靠且高效的化学方法。所提出的策略包括使用N-碘代琥珀酰亚胺对核苷三磷酸进行区域选择性碘化,然后通过钯催化的与烯丙胺的Heck偶联反应,以良好的产率提供相应的(E)-5-氨基烯丙基-尿苷-5'-O-三磷酸。值得注意的是,该方案不仅提供了高纯度的产物,还避免了使用有毒的汞试剂。© 2017约翰威立国际出版公司。