Synthesis and antiviral activity of N⁹-[3-fluoro-2-(phosphonomethoxy)propyl] analogues derived from N⁶-substituted adenines and 2,6-diaminopurines
An efficient method for the synthesis of N⁹-[3-fluoro-2-(phosphonomethoxy)propyl] (FPMP) derivatives of purine bases has been developed. Both (R)- and (S)-enantiomers of the N⁶-substituted FPMP derivatives of adenine and 2,6-diaminopurine were prepared and their anti-human immunodeficiency virus (HI...
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Veröffentlicht in: | Bioorganic & medicinal chemistry 2011-04, Vol.19 (7), p.2114-2124 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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