A convenient and efficient synthesis of a novel class of acyclic nucleoside phosphonates derived from 2-(phosphonomethoxy)propanoic acid has been developed. The key step of the synthesis is the optimized oxidation of the 3-hydroxy-2-(phosphonomethoxy)propyl (HPMP) analogues to the corresponding 2'-carboxy-PME (CPME) derivatives using the TEMPO/NaClO/NaClO oxidizing system. Although ()-3-(adenin-9-yl)-2-(phosphonomethoxy)propanoic acid (()-CPMEA) has been designed as a compound with potential anti-HIV activity, none of the newly prepared CPME analogues exhibited any antiviral activity.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111817 | PMC |
http://dx.doi.org/10.1016/j.tet.2012.03.066 | DOI Listing |
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