• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 150
  • 24
  • 15
  • 15
  • 15
  • 15
  • 15
  • 15
  • 15
  • 7
  • 6
  • 3
  • 2
  • 2
  • 1
  • Tagged with
  • 344
  • 123
  • 117
  • 116
  • 74
  • 72
  • 72
  • 66
  • 59
  • 43
  • 40
  • 40
  • 36
  • 35
  • 31
  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
51

Synthesis of D, L-2'-epi-showdomycin and -pyrazofurin A and of D,L-2'-deoxyshowdomycin by Mu-Ill Lim.

Lim, Mu-Ill January 1976 (has links)
No description available.
52

Synthetic approaches to novel adenosine analogues and the synthesis of potential antiviral agents

Thorpe, Andrew John January 1993 (has links)
No description available.
53

Syntheses of carbocyclic analogues of c-nucleosides

Ouellet, René January 1975 (has links)
No description available.
54

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

Boisvert, Suzanne, 1955- January 1986 (has links)
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. / 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. / 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.
55

An approach to carbocyclic analogues of C-nucleosides.

Reader, Grant William. January 1973 (has links)
No description available.
56

Studies on the methylation of cytidine

Kader, Harvey A. (Harvey Abraham) January 1982 (has links)
No description available.
57

Untersuchung zur Eignung renal ausgeschiedener modifizierter Nukleoside in der Frühdiagnostik und in der Verlaufskontrolle von nicht-kleinzelligen Bronchialkarzinomen

Pastaschek, Heidi Elisabeth 03 January 2012 (has links) (PDF)
Untersuchung zur Eignung renal ausgeschiedener modifizierter Nukleoside in der Frühdiagnostik und in der Verlaufskontrolle von nicht-kleinzelligen Bronchialkarzinomen
58

Polynucleotide studies.

Schmitz, Kenneth S., January 1972 (has links)
Thesis (Ph. D.)--University of Washington. / Includes bibliographies.
59

Studies of psi synthase RluA with a potent inhibitor RNA containing 5-fluorouridine /

Vizthum, Caroline A. January 2008 (has links)
Thesis (M.S.)--University of Delaware, 2007. / Principal faculty advisor: Eugene G. Mueller, Dept. of Chemistry & Biochemistry. Includes bibliographical references.
60

Synthesis of carbon and glycosylated nucleosides /

Mladenova, Gabriela. January 2006 (has links)
Thesis (Ph.D.)--York University, 2006. Graduate Programme in Chemistry. / Typescript. Includes bibliographical references (leaves 113-125). Also available on the Internet. MODE OF ACCESS via web browser by entering the following URL: http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:NR29510

Page generated in 0.0681 seconds