Institut des Biomolécules Max Mousseron (IBMM), UMR 5247 CNRS, Université de Montpellier, ENSCM , Campus Triolet, cc 1705, Place Eugène Bataillon, 34095 Montpellier cedex 5, France.
Chem Rev. 2016 Jul 27;116(14):7854-97. doi: 10.1021/acs.chemrev.6b00174. Epub 2016 Jun 20.
Focusing on the recent literature (since 2000), this review outlines the main synthetic approaches for the preparation of 5'-mono-, 5'-di-, and 5'-triphosphorylated nucleosides, also known as nucleotides, as well as several derivatives, namely, cyclic nucleotides and dinucleotides, dinucleoside 5',5'-polyphosphates, sugar nucleotides, and nucleolipids. Endogenous nucleotides and their analogues can be obtained enzymatically, which is often restricted to natural substrates, or chemically. In chemical synthesis, protected or unprotected nucleosides can be used as the starting material, depending on the nature of the reagents selected from P(III) or P(V) species. Both solution-phase and solid-support syntheses have been developed and are reported here. Although a considerable amount of research has been conducted in this field, further work is required because chemists are still faced with the challenge of developing a universal methodology that is compatible with a large variety of nucleoside analogues.
本文聚焦于 2000 年以来的最新文献,概述了 5'-单-、5'-二-和 5'-三磷酸化核苷(也称为核苷酸)以及几种衍生物(即环核苷酸和二核苷酸、二核苷 5',5'-聚磷酸酯、糖核苷酸和核苷脂质)的主要合成方法。内源性核苷酸及其类似物可以通过酶法获得,这通常限于天然底物,或者通过化学方法获得。在化学合成中,可以使用保护或未保护的核苷作为起始材料,具体取决于所选的 P(III)或 P(V)物种的试剂的性质。本文报道了液相和固相合成的发展情况。尽管该领域已经进行了相当多的研究,但由于化学家仍然面临着开发与各种核苷类似物兼容的通用方法的挑战,因此仍需要进一步的工作。