31p NMR studies on oxidative transformations of aryl nucleoside h-phosphonate diesters

Article abstract of DOI:10.1080/15257779908041625

Various aspects of oxidative coupling of nucleoside aryl H-phosphonate diesters with nucleosides to produce important synthetic intermediates in the phosphotriester approach to oligonucleotide synthesis, dinucleoside aryl phosphotriesters, was investigated. Copyright

Full text of DOI:10.1080/15257779908041625

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Nucleosides and Nucleotides
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31P NMR Studies on Oxidative
Transformations of Aryl Nucleoside H-
Phosphonate Diesters
Annika Kers a , Inger Kers a , Jacek Cieslak b , Adam Kraszewski b &
Jacek Stawinski a
a Department of Organic Chemistry, Arrhenius Laboratory ,
Stockholm University , S-106 91, Stockholm, Sweden
b Institute of Bioorganic Chemistry, Polish Academy of Sciences ,
Noskowskiego 12/14, 61-704, Poznan, Poland
Published online: 04 Oct 2006.
To cite this article: Annika Kers , Inger Kers , Jacek Cieslak , Adam Kraszewski & Jacek Stawinski
(1999) 31P NMR Studies on Oxidative Transformations of Aryl Nucleoside H-Phosphonate Diesters,
Nucleosides and Nucleotides, 18:4-5, 991-992, DOI: 10.1080/15257779908041625
To link to this article: http://dx.doi.org/10.1080/15257779908041625
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