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dc.contributor.advisorMohammad Movassaghi.en_US
dc.contributor.authorAvci, Nadide Hazal.en_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Chemistry.en_US
dc.date.accessioned2020-10-18T21:39:54Z
dc.date.available2020-10-18T21:39:54Z
dc.date.copyright2020en_US
dc.date.issued2020en_US
dc.identifier.urihttps://hdl.handle.net/1721.1/128073
dc.descriptionThesis: S.M., Massachusetts Institute of Technology, Department of Chemistry, 2020en_US
dc.descriptionCataloged from PDF of thesis.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstractSynthesis and optimization of C21-oxygenated pentacyclic aspidosperma core is described. A highly effective enzymatic resolution of a non-[beta]-branched primary alcohol (E=22) allowed rapid preparation of both enantiomeric forms of a C21-oxygenated precursor for synthesis of aspidosperma alkaloids.en_US
dc.description.statementofresponsibilityby Nadide Hazal Avci.en_US
dc.format.extent25 pagesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectChemistry.en_US
dc.titleSynthesis and optimization of synthetic intermediates to access C21-oxygenated aspidosperma alkaloidsen_US
dc.typeThesisen_US
dc.description.degreeS.M.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.identifier.oclc1199132256en_US
dc.description.collectionS.M. Massachusetts Institute of Technology, Department of Chemistryen_US
dspace.imported2020-10-18T21:39:51Zen_US
mit.thesis.degreeMasteren_US
mit.thesis.departmentChemen_US


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