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Stereochemical studies on hemiorthoester tetrahedral intermediates - by Riwa A. Dandan

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dc.contributor.author Dandan, Riwa A.
dc.date.accessioned 2012-06-13T06:39:04Z
dc.date.available 2012-06-13T06:39:04Z
dc.date.issued 1984
dc.identifier.uri http://hdl.handle.net/10938/3965
dc.description Thesis (M.S.)--American University of Beirut. Department of Chemistry, 1984.;"Advisor: Farid Khoury, Associate Professor, Laboratory Medicine -- Members of Committee: Makhlouf Haddadin, Professor, Chemistry Mary Kasparian, Lecturer, Chemistry."
dc.description Bibliography: leaves 59-65.
dc.description.abstract Hydrolysis of 11-iodo- δ -undecalactone 54 gave 5-hydroxy-ll-iodoundecanoic acid 62. Cyclization of the cesium salt of 62 afforded 5-hydroxy-w-dodecalactone 50 and its diolide 64 as an inseparable mixture. Protection of the hydroxy group in 62, prior to c
dc.format.extent [viii], 65 leaves : ill. cm.
dc.language.iso eng
dc.relation.ispartof Theses, Dissertations, and Projects
dc.subject.classification T:003183 AUBNO
dc.subject.lcsh Esters.
dc.subject.lcsh Polyesters.
dc.subject.lcsh Stereochemistry.
dc.title Stereochemical studies on hemiorthoester tetrahedral intermediates - by Riwa A. Dandan
dc.type Thesis
dc.contributor.department American University of Beirut. Faculty of Arts and Sciences. Department of Chemistry


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