The prooligonucleotide approach. I: Esterase-mediated reversibility of dithymidine S-alkyl-phosphorothiolates to dithymidine phosphorothioates
- 29 March 1995
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 5 (6) , 563-568
- https://doi.org/10.1016/0960-894x(95)00074-4
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Rational design for cytosolic delivery of nucleoside monphosphates : “SATE” and “DTE” as enzyme-labile transient phosphate protecting groupsPublished by Elsevier ,2001
- Stereospecific bio-reversibility of dinucleoside S-alkyl phosphorothiolates to dinucleoside phosphorothioatesBioorganic & Medicinal Chemistry Letters, 1994
- Intracellular delivery of nucleoside monophosphates through a reductase-mediated activation processAntiviral Research, 1993
- Site-specific labeling of DNA sequences containing phosphorothioate diestersJournal of the American Chemical Society, 1992
- Nucleoside H-Phosphonates. XI. A Convenient Method for the Preparation of Nucleoside H-PhosphonatesNucleosides and Nucleotides, 1990
- Nucleoside H-phosphonates. X. Studies on nucleoside hydrogenphosphonothioate diester synthesisTetrahedron Letters, 1989
- DNA and RNA Sequence Determination Based on Phosphorothioate ChemistryScience, 1988
- Why Nature Chose PhosphatesScience, 1987
- 2-lodoethyl Esters from Acyl Chlorides, Ethylene Oxide, and Sodium IodideSynthesis, 1982
- Mechanisms of Nucleophilic Substitution in Phosphate EstersChemical Reviews, 1964