Use of ammonium aryl H-phosphonates in the preparation of nucleoside H-phosphonate building blocks
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. The chemical synthesis of oligo- and poly-nucleotides by the phosphotriester approach
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3. Synthesis of S-alkyl esters of protected 2′-deoxyribonucleoside 3′-phosphorothioates. Building blocks for the large-scale synthesis of phosphorothioate analogues of oligodeoxyribonucleotides by the phosphotriester approach in solution
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1. ChemInform Abstract: Use of Ammonium Aryl H-Phosphonates in the Preparation of Nucleoside H- Phosphonate Building Blocks.;ChemInform;2010-08-04
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3. Recent Advances in the Chemical Synthesis of RNA;Current Protocols in Nucleic Acid Chemistry;2009-09
4. Synthesis of 3’,5’-cyclic diguanylic acid (cdiGMP) Using 1-(4-chlorophenyl)-4-ethoxypiperidin-4-yl as a Protecting Group for 2’-hydroxy Functions of Ribonucleosides;Nucleosides, Nucleotides and Nucleic Acids;2007-03
5. Synthesis of mono- and di-sialophospholipids via the H-phosphonate approach;Canadian Journal of Chemistry;2006-04-01
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