Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters











Database
Language
Publication year range
1.
Article in English | MEDLINE | ID: mdl-16252666

ABSTRACT

A solution of sulfur (0.1 M) and sodium sulfide (0.01M) in 3-picoline, referred to as polysulfide reagent, rapidly converts trialkyl and triaryl phosphite triesters to the corresponding phosphorothioate derivatives. Greater than 99.8% average stepwise sulfurization efficiency is obtained in the solid-phase synthesis of DNA and RNA phosphorothioate olgonucleotides via the phosphoramidite approach.


Subject(s)
Biochemistry/methods , Oligonucleotides/chemical synthesis , Organothiophosphorus Compounds/chemistry , Sulfides/chemistry , Chromatography, High Pressure Liquid , Oligonucleotides/chemistry , Organothiophosphorus Compounds/chemical synthesis
2.
Bioorg Med Chem Lett ; 14(18): 4683-90, 2004 Sep 20.
Article in English | MEDLINE | ID: mdl-15324888

ABSTRACT

Incomplete sulfurization during solid-phase synthesis of phosphorothioate oligonucleotides using phosphoramidite chemistry was identified as the cause of formation of two new classes of process-related oligonucleotide impurities containing a DMTr-C-phosphonate (DMTr=4,4'-dimethoxytrityl) moiety. Phosphite triester intermediates that failed to oxidize (sulfurize) to the corresponding phosphorothioate triester react during the subsequent acid-induced (dichloroacetic acid) detritylation with the DMTr cation or its equivalent in an Arbuzov-type reaction. This leads to formation of DMTr-C-phosphonate mono- and diesters resulting in oligonucleotides modified with a DMTr-C-phosphonate moiety located internally or at the 5'terminal hydroxy group. DMTr-C-phosphonate derivatives are not detected when optimized sulfurization conditions are employed.


Subject(s)
Oligonucleotides/chemical synthesis , Organophosphonates/chemical synthesis , Trityl Compounds/chemical synthesis , Chromatography, High Pressure Liquid , Oligonucleotides/chemistry , Organophosphonates/chemistry , Phosphites/chemistry , Structure-Activity Relationship , Trityl Compounds/chemistry , Trityl Compounds/pharmacology
3.
Nucleosides Nucleotides Nucleic Acids ; 23(5): 767-75, 2004 May.
Article in English | MEDLINE | ID: mdl-15281365

ABSTRACT

The impuritiy profiles of acetonitrile solutions of the four standard O-cyanoethyl-N,N-diisopropyl-phosphoramidites of 5'-O-dimethoxytrityl (DMT) protected deoxyribonucleosides (dG(ib), dA(bz), dC(bz), T) were analyzed by HPLC-MS. The solution stability of the phosphoramidites decreases in the order T, dC>dA>dG. After five weeks storage under inert gas atmosphere the amidite purity was reduced by 2% (T, dC), 6% (dA), and 39% (dG), respectively. The main degradation pathways involve hydrolysis, elimination of acrylonitrile and autocatalytic acrylonitrile-induced formation of cyanoethyl phosphonoamidates. Consequently, the rate of degradation is reduced by reducing the water concentration in solution with molecular sieves and by lowering the amidite concentration. Acid-catalyzed hydrolysis could also be reduced by addition of small amounts of base.


Subject(s)
Acetonitriles/chemistry , Deoxyribonucleosides/chemistry , Organophosphorus Compounds/chemistry , Deoxyribonucleosides/metabolism , Solutions
SELECTION OF CITATIONS
SEARCH DETAIL