Academic literature on the topic 'Antiviral nucleosides'

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Dissertations / Theses on the topic "Antiviral nucleosides"

1

Popescu, Anne. "Racemic carbocyclic nucleosides and their anti-viral activity." Lund : Lund University Chemical Center, 1995. http://books.google.com/books?id=5vhqAAAAMAAJ.

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2

He, Mingzhu Schneller Stewart W. "Carbocyclic C-nucleosides derived from formycin." Auburn, Ala, 2008. http://hdl.handle.net/10415/1427.

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3

Shi, Houguang. "Synthesis and Antiviral Evaluation of Some 3'-Carboxymethyl-3'-deoxyadenosine Derivatives." Diss., CLICK HERE for online access, 2007. http://contentdm.lib.byu.edu/ETD/image/etd1940.pdf.

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4

Harrison, M. "Synthesis of acyclic c-nucleosides as potential antiviral agents." Thesis, Heriot-Watt University, 1988. http://hdl.handle.net/10399/1004.

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5

Bouali, Abderrahime. "#beta#-D-ketofuranosyl purine nucleosides as potential antiviral agents." Thesis, University of Lincoln, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.359008.

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6

Boisvert, Suzanne 1955. "Preparation of novel heterocyclic-ring analogues of BIOLF-62 : application of 29SI NMR nucleosides and the investigation of 2,4-dinitrobenzenesulfenyl as a protecting group for ribonucleotide synthesis." Thesis, McGill University, 1986. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=75365.

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In light of the remarkable antiviral activity of acyclic nucleoside analogues such as that of BIOLF-62 against the herpes viruses, a number of products in which heterocyclic bases were coupled to the active acyclic sugar moiety were prepared and submitted for biological testing.<br>Various dimethoxytritylated and t -butyldimethylsilylated derivatives of arabinoadenosine were prepared and fully characterised by $ sp1$H and $ sp{13}$C NMR spectroscopy. $ sp{29}$Si INEPT as well as $ sp{29}$Si-$ sp1{ rm H}$ correlated NMR were used to study various t -butyldimethylsilyl and triisopropylsilyl substituted ribonucleosides.<br>In an effort aimed at the development of new and better nucleoside protecting functions, the 2,4-dinitrobenzenesulfenyl group which is stable to both acidic and basic conditions, was used for $5 sp prime$-hydroxyl protection of ribonucleosides and its compatibility with the phosphodichoridite nucleoside coupling procedure was investigated. The nitrobenzenesulfenyl group was used in conjunction with the dimethoxytrityl group for $2 sp prime$-hydroxyl protection in the synthesis of a UpU dimer. The latter was fully characterised by enzymatic degradation and HPLC analysis of the products.
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7

Shulyak, Tetyana S. "Exploring sinefungin analogs as potential antiviral agents." Auburn, Ala., 2005. http://repo.lib.auburn.edu/2005%20Summer/doctoral/SHULYAK_TETYANA_14.pdf.

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8

Clark, Sarah Alexandra. "The synthesis of 2-fluoromethyl nucleosides as potential antiviral agents." Thesis, Queen's University Belfast, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.492322.

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Nucleoside analogues are a vital class ofcompounds that are used in the treatment of AIDS and other viral infections. Research into the synthesis of2'-C-fluoromethyl cytosine is described. The key step in the synthesis involves the fluorination ofthe 2-Chydroxymethyl derivative of ribose with Deoxo-Fluoi'lY. The 2-C-hydroxymethyl compound is readily prepared from D-ribose on a multigram scale. Research was carried out into the synthesis of2', 3'-dideoi\.')'-2'-C-fluoromethyl-3'-Chydroxymethyl nucleosides using various different methodologies and a few different starting materials, including D-mannitol and O-benzyl-DL-serine. The key steps consisted ofthe production ofa Z-isomer in a Wittig reaction which could then cyclise to form a butenolide. Once this key component had been formed, a regio- and stereoselective photocatalysed addition ofmethanol was carried out. Supplied by The British Library - 'The world's knowledge'
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9

Angell, Annette. "The design, synthesis and evaluation of some novel antiviral nucleosides." Thesis, Cardiff University, 2005. http://orca.cf.ac.uk/55384/.

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An investigation into the pH stability of the BCNAs was also carried out and the parent analogue bearing a pentyphenyl side chain was found to be stable at a range of pHs. Finally, with the X-ray crystal structure of VZV thymidine kinase published we began a preliminary investigation into the possible interaction the BCNAs with this enzyme using molecular modelling
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10

Gould, Jayne H. M. "The synthesis of novel nucleosides and nucleotides as potential antiviral agents." Thesis, University of Reading, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.339518.

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