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Recent Trends in Nucleotide Synthesis

Roy, Béatrice, Depaix, Anaïs, Périgaud, Christian, Peyrottes, Suzanne·2016·Chemical Reviews

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.

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Metadata

Authors
Roy, B., Depaix, A., Périgaud, C., & Peyrottes, S.
Venue
Chemical Reviews
Published
2016-06-20
Volume
116
Issue
14
Pages
7854-7897
ISSN
  • 0009-2665 (ISSN-L)
  • 1520-6890
OpenAlex
W2463920377
Cited by
212
References
1
FWCI
0.50
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Recent Trends in Nucleotide Synthesis. https://app.cochat.ai/papers/10.1021/acs.chemrev.6b00174
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Roy, B., Depaix, A., Périgaud, C., & Peyrottes, S. (2016). Recent Trends in Nucleotide Synthesis. Chemical Reviews. https://doi.org/10.1021/acs.chemrev.6b00174

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