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 |