Ruthenium tetraoxide: a mild reagent for the oxidation of 2′,3′-O-isopropylidene purine nucleosides
- 1 April 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (17) , 2307-2310
- https://doi.org/10.1016/s0040-4039(00)74197-9
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Efficient oxidation of phenyl groups to carboxylic acids with ruthenium tetraoxide. A simple synthesis of (R)-.gamma.-caprolactone, the pheromone of Trogoderma granariumThe Journal of Organic Chemistry, 1990
- A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compoundsThe Journal of Organic Chemistry, 1981
- Modification of the 5' position of purine nucleosides. 2. Synthesis and some cardiovascular properties of adenosine-5'-(N-substituted)carboxamidesJournal of Medicinal Chemistry, 1980
- Modification of the 5' position of purine nucleosides. 1. Synthesis and biological properties of alkyl adenosine-5'-carboxylatesJournal of Medicinal Chemistry, 1976
- Metabolic effects of ethyl adenosine 5′-carboxylate in Ehrlich ascites tumor cells in vitroBiochemical Pharmacology, 1976
- Ringverengung bei 1.2-diazepin-anionen - valenzisomerisierung cyclisch konjugierter 4nπ-systemeTetrahedron Letters, 1972
- Conversion of 2',3'-O-isopropylideneadenosine into the 5',5'-di-C-methyl derivativeThe Journal of Organic Chemistry, 1970
- Synthese 5′‐modifizierter AdenosinderivateEuropean Journal of Inorganic Chemistry, 1968
- 212. Nucleotides. Part XLVII. The catalytic oxidation of nucleosides and nucleotides: a projected stepwise degradation of polynucleotidesJournal of the Chemical Society, 1963