## Abstract A new series of mononucleotide analogues bearing a nonhydrolysable P–C bond instead of the P–O phosphate linkage is presented. We intend to set up an approach that allows the synthesis of β‐hydroxyphosphonate nucleoside analogues as a single diastereoisomer. In this respect, the key “su
Synthesis of Pyrimidine-Containing Nucleoside β-(R/S)-Hydroxyphosphonate Analogues
✍ Scribed by Maïa Meurillon; Laurent Chaloin; Christian Périgaud; Suzanne Peyrottes
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 1008 KB
- Volume
- 2011
- Category
- Article
- ISSN
- 1434-193X
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✦ Synopsis
Abstract
A concise route to nucleoside β‐hydroxyphosphonate analogues is described. The use of a nucleoside β‐ketophosphonate as the key intermediate allowed both the (R) and (S) isomers of β‐hydroxyphosphonate analogues in the pyrimidine series to be accessed. Such derivatives may be considered as stable mimics of 5′‐monophosphate nucleosides and, therefore, could be the starting point for the development of potential therapeutic agents.
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