Reaction of pivaloyl chloride with internucleosidic h-phosphonate diesters
Author:
Funder
Dutch Foundation
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/recl.19861051106/fullpdf
Reference11 articles.
1. Nucleoside H-phosphonates. III. Chemical synthesis of oligodeoxyribonucleotides by the hydrogenphosphonate approach
2. Nucleoside h-phosphonates: Valuable intermediates in the synthesis of deoxyoligonucleotides
3. Synthesis of DNA via deoxynudeoside H-phosphonate Intermediates
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1. A general procedure to convert H-phosphonate mono- or diesters of nucleic acids into valuable phosphate di- or triesters;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. Preparation of internucleotide phosphate analogues via the corresponding H-phosphonate diester;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
3. Phosphorylation of benzyl-protected sugar derivatives via 1-H-phosphonate intermediates: Synthesis of DL-myo-inositol 1,4,5-tris-1-H-phosphonate;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
4. Synthesis of Oligodeoxyribo‐ and Oligoribonucleotides According to the H ‐Phosphonate Method;Current Protocols in Nucleic Acid Chemistry;2004-12
5. BH 3 as a protecting group for phosphonic acid: a novel method for the synthesis of dinucleoside H -phosphonate;Tetrahedron Letters;2004-01
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