50571-26-1Relevant articles and documents
First synthesis of carbocyclic oligothymidylates
Szemzo,Szecsi,Sagi,Otvos
, p. 1463 - 1466 (1990)
5'-O-(dimethoxytrityl)-(+)-carbocyclic thymidine 1 is converted into different 3'-substituted intermediates 2a-c following standard procedures. From these compounds stereochemically pure carbocyclic oligothymidylates 4 are obtained using solid phase synthetic methods.
Nucleoside H-phosphonates, XXII: Synthesis and properties of new nucleotide analogues - H-phosphonothiolate diesters
Hiresova, Renata,Stawinski, Jacek
, p. 2748 - 2752 (2008/03/14)
Condensation of nucleoside 3′-H-phosphonate monoesters with various thiols, promoted by condensing agents, provides a convenient access to a new class of H-phosphonate analogues, H-phosphonothiolate diesters. Chemical properties, relevant to possible appl
Use of ammonium aryl H-phosphonates in the preparation of nucleoside H-phosphonate building blocks
Ozola, Vita,Reese, Colin B.,Song, Quanlai
, p. 8621 - 8624 (2007/10/03)
Ammonium 4-methylphenyl H-phosphonate 4c was used in the conversion of 5'-0-(dimethoxy-trityl)-2'-deoxynucleoside derivatives 6 into the corresponding 3'-H-phosphonates 2, which were isolated in a high state of purity and in high yield.