Acyclic nucleoside bisphosphonates: synthesis and properties of chiral 2-amino-4,6-bis[(phosphonomethoxy)alkoxy]pyrimidines

. 2009 Jun ; 44 (6) : 2408-24. [epub] 20081002

Jazyk angličtina Země Francie Médium print-electronic

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid18992968

Grantová podpora
UC1 AI062540 NIAID NIH HHS - United States
UC1 AI062540-01 NIAID NIH HHS - United States
1UC1AI062540-01 NIAID NIH HHS - United States

Odkazy

PubMed 18992968
PubMed Central PMC2706328
DOI 10.1016/j.ejmech.2008.09.031
PII: S0223-5234(08)00454-6
Knihovny.cz E-zdroje

2-Amino-4,6-bis[(phosphonomethoxy)alkoxy]pyrimidines bearing two equal or different achiral or chiral phosphonoalkoxy chains have been prepared either by aromatic nucleophilic substitution of 2-amino-4,6-dichloropyrimidine or by alkylation of 4,6-dihydroxy-2-(methylsulfanyl)pyrimidine with appropriate phosphonate-bearing building block. Alkylation of 4,6-dihydroxy-2-(methylsulfanyl)pyrimidine proved to be the method of choice for efficient preparation of variety of bisphosphonates. The enantiomeric purity of selected compounds was determined by capillary electrophoresis. Antiviral activity of bisphosphonates is discussed.

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