Spelling suggestions: "subject:"nucleoside""
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Synthesis of carbocyclic analogues of C-nucleosidesChalard-Faure, Bernadette G. January 1975 (has links)
No description available.
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The synthesis of silylated arabinopyrimidine nucleosides : a thesisMcGee, Danny P. C. January 1981 (has links)
No description available.
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The synthesis of silylated arabinopyrimidine nucleosides : a thesisMcGee, Danny P. C. January 1981 (has links)
No description available.
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Carbocyclic C-nucleosides derived from formycinHe, Mingzhu. Schneller, Stewart W., January 2008 (has links)
Thesis (Ph. D.)--Auburn University. / Abstract. Vita. Includes bibliographical references (p. 110-125).
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Ondersoek na die gebruik van ditioasetale van aldoses in die sintese van C-glikosiede22 October 2015 (has links)
D.Sc. (Chemistry) / Please refer to full text to view abstract
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Erythrocyte nucleoside transporters: photoaffinity labelling, isolation and molecular studies.January 1987 (has links)
by Francis Yat Ping Kwong. / Thesis (Ph.D.)--Chinese University of Hong Kong, 1987. / Bibliography: leaves [135]-[152]
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The synthesis of nucleoside and silyl nucleotide analogues /Cormier, James January 1987 (has links)
No description available.
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The synthesis of nucleoside and silyl nucleotide analogues /Cormier, James January 1987 (has links)
A route to the synthesis of arabino and xylonucleosides is described. This route takes advantage of highly selective ribonucleoside hydroxyl protection procedures which have recently been developed. The route is straightforward and broadly applicable. It may be applied to both purine and pyrimidine nucleosides. Synthesis, deprotection, and characterisation of the target compounds are described. The work is compared to that of others in the field. / A novel class of oligonucleotide analogues is described. In this group, the phosphorus atom of the internucleotide link is replaced by silicon. The synthesis of both oligothymidine and oligo-2$ sp prime$-deoxyadenosine nucleotide analogues of this class is described. Various substituents at silicon are employed, and oligonucleotide analogs of up to six units long are synthesised, characterised and deprotected. The circular dichroism spectra of the deprotected hexamers is presented.
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Synthesis and properties of novel nucleoside and nucleotide analogues : a thesisGillen, Michael Francis. January 1980 (has links)
The synthesis of novel nucleoside and nucleotide analogues in which the sugar moiety is replaced by an aliphatic chain is described. The acyclic analogue of adenosine was tested as both a substrate and an inhibitor of adenosine deaminase while the interaction of some dinucleoside monophosphate analogues with spleen and snake venom phosphodiesterase is reported. Some mention is made of the solution conformation of these acyclic derivatives. / The utility of the methyl group as a phosphate protecting group in oligonucleotide synthesis was reinvestigated and the preparation of some interesting 2', 5' linked trinucleoside diphosphate analogues of adenosine, with the methyl moiety as phosphate masking group, was undertaken. A novel approach to the cleavage of phosphate methyl esters is discussed. / A facile fluoride ion mediated preparation of alkylated nucleoside base fragments was discovered. This procedure led to high isolated yields of a variety of N-alkylated purines and pyrimidines.
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The role of the human mitochondrial polymerase in the toxicity of nucleoside analogs and agingHanes, Jeremiah Wayne, Johnson, Kenneth A., January 2004 (has links) (PDF)
Thesis (Ph. D.)--University of Texas at Austin, 2004. / Supervisor: Kenneth A. Johnson. Vita. Includes bibliographical references.
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