Nucleoside 4',5'-enol acetates. Synthesis and chemistry of a unique uridine O2,4'-anhydronucleoside
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- Type
- article
- Published
- 1979-03-01
- Cited by
- 27
- References
- 1
- OpenAlex
- https://openalex.org/W2028449191
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:84255908
Keywords
Uridine, Chemistry, Nucleoside, Enol, Stereochemistry
References
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Cited by
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- Synthesis of Several Types of Bridged Nucleic Acids
- THE CHEMISTRY OF 4′,5′-UNSATURATED NUCLEOSIDES. A REVIEW
- Synthesis of (3R,4S)-3,4,5-Trihydroxy-4-methylpentylphosphonic Acid as a Potential Inhibitor of the Nonmevalonate Pathway
- A 9-step enantiospecific synthesis of (-)-aristeromycin from D-ribonic acid γ-lactone
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- Synthesis of P-5 tethered inositol-1,2,6-trisphosphate, an affinity reagent for α-trinositol receptors
- Chemoenzymatic synthesis of glucose fatty esters.
- A SIMPLE STEREOSELECTIVE ONE POT CONVERSION OF COMPOUNDS WITH A DIMETHYLAMINOMETHYLENE GROUP INTO ENOL ESTERS
- Conformationally restricted spin labelled nucleotides: a model study of the synthesis and properties of the 2′,3′-O-spiro ketal of uridine and 4-oxo-2,2,6,6-tetramethyl-1-piperidyloxy
- Essential reactive intermediates in nucleoside chemistry: cyclonucleoside cations.
- Comparison of the substrate specificity of type I and type II dehydroquinases with 5-deoxy- and 4,5-dideoxy-dehydroquinic acid
- SYNTHESIS AND CONFORMATION OF 3'-O,4'-C-METHYLENERIBONUCLEOSIDES, NOVEL BICYCLIC NUCLEOSIDE ANALOGUES FOR 2',5'-LINKED OLIGONUCLEOTIDE MODIFICATION
- Synthesis of 4′-Trifluoromethyl Nucleoside Analogs
- Nucleosidic enol esters: A versatile tool for the synthesis of 3′-carbon-substituted nucleosides
- BNAs: novel nucleic acid analogs with a bridged sugar moiety.
- A Ferrier-type allylic rearrangement of 3'-deoxy-3',4'-didehydronucleosides mediated by DMF dimethyl acetal: direct access to 4'-alkoxy-2',3'-didehydro-2',3'-dideoxynucleosides.
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