| Literature DB >> 27319940 |
Béatrice Roy1, Anaïs Depaix1, Christian Périgaud1, Suzanne Peyrottes1.
Abstract
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.Entities:
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Year: 2016 PMID: 27319940 DOI: 10.1021/acs.chemrev.6b00174
Source DB: PubMed Journal: Chem Rev ISSN: 0009-2665 Impact factor: 60.622