Use of ammonium aryl H-phosphonates in the preparation of nucleoside H-phosphonate building blocks
- 18 November 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (47) , 8621-8624
- https://doi.org/10.1016/0040-4039(96)01993-4
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- 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 solutionJournal of the Chemical Society, Perkin Transactions 1, 1995
- Rates and mechanisms of hydrolysis of esters of phosphorous acidJournal of the American Chemical Society, 1988
- Synthesis of DNA via deoxynudeoside H-phosphonate IntermediatesNucleic Acids Research, 1986
- A convenient and general approach to the synthesis of properly protected d-nucleoside-3′-hydrogenphosphonates via phosphite intermediatesTetrahedron Letters, 1986
- Nucleoside h-phosphonates: Valuable intermediates in the synthesis of deoxyoligonucleotidesTetrahedron Letters, 1986
- The protection of thymine and guanine residues in oligodeoxyribonucleotide synthesisJournal of the Chemical Society, Perkin Transactions 1, 1984
- Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesisTetrahedron Letters, 1981
- The protection of uracil and guanine residues in oligonucleotide synthesisTetrahedron Letters, 1981
- The chemical synthesis of oligo- and poly-nucleotides by the phosphotriester approachTetrahedron, 1978