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Synthesis of 3, 4-substituted cyclopentanols as potential precursors to nucleoside analogs - by Manal Sami Farah

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dc.contributor.author Farah, Manal Sami
dc.date.accessioned 2012-06-13T07:10:50Z
dc.date.available 2012-06-13T07:10:50Z
dc.date.issued 2007
dc.identifier.uri http://hdl.handle.net/10938/7514
dc.description Thesis (M.A.)--American University of Beirut, Dept. of Chemistry, 2007.;"Advisor: Dr. Kamal Bouhadir, Associate Professor, Chemistry--Member of Committee: Dr. Makhlouf Haddadin, Professor, Chemistry--Member of Committee: Dr. Tarek Ghaddar, Assistant Proff
dc.description Bibliography: leaves 63-66.
dc.description.abstract Four carbocyclic nucleosides have been formed from two 3,4-disubstituted cyclope ntanols derivatives via the Mitsunobu reaction. Three steps, starting from trans -cyclohex-4-ene-1,2-dicarboxylic acid diethyl ester, have been used to form the first derivat
dc.format.extent xiii, 66 leaves : ill. 30 cm.
dc.language.iso eng
dc.relation.ispartof Theses, Dissertations, and Projects
dc.subject.classification T:004864 AUBNO
dc.subject.lcsh Cyclopentane
dc.subject.lcsh Nucleosides -- Synthesis
dc.subject.lcsh Oligonucleotides -- Synthesis
dc.title Synthesis of 3, 4-substituted cyclopentanols as potential precursors to nucleoside analogs - by Manal Sami Farah
dc.type Thesis
dc.contributor.department American University of Beirut. Faculty of Arts and Sciences. Department of Chemistry


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