Depaix Anaïs, Peyrottes Suzanne, Roy Béatrice
Institut des Biomolécules Max Mousseron (IBMM), UMR 5247 CNRS, Université de Montpellier, ENSCM, Campus Triolet, Montpellier, France.
Curr Protoc Nucleic Acid Chem. 2017 Jun 19;69:13.16.1-13.16.11. doi: 10.1002/cpnc.30.
This unit describes a one-pot, two step synthesis of ribonucleoside 5'-di- and 5'-triphosphates, as well as their purification. The first step of the synthesis involves the activation of an unprotected ribonucleoside 5'-monophosphate with 2-chloro-1,3-dimethylimidazolinium hexafluorophosphate and imidazole, in a mixture of water/acetonitrile. The resulting phosphorimidazolate intermediate is then treated with inorganic phosphate or pyrophosphate to afford the corresponding nucleoside 5'-di- or 5'-triphosphates. The attractive features of this strategy include the absence of protecting groups on the starting material and convenient set up (i.e., use of water, non-dry solvents and reagents, commercially available sodium salts). © 2017 by John Wiley & Sons, Inc.
本单元描述了核糖核苷5'-二磷酸和5'-三磷酸的一锅两步合成及其纯化方法。合成的第一步是在水/乙腈混合物中,用2-氯-1,3-二甲基咪唑六氟磷酸盐和咪唑对未保护的核糖核苷5'-单磷酸进行活化。然后将所得的磷酰咪唑盐中间体用无机磷酸盐或焦磷酸盐处理,得到相应的核苷5'-二磷酸或5'-三磷酸。该策略的吸引人之处包括起始原料上无需保护基团以及设置方便(即使用水、非干燥溶剂和试剂、市售钠盐)。© 2017约翰威立父子公司。