One-pot synthesis of tetrasubstituted isoindolinones

dc.contributor.advisorEisler, Sara
dc.contributor.authorAlmansour, Milhah
dc.date.accessioned2023-03-01T16:35:16Z
dc.date.available2023-03-01T16:35:16Z
dc.date.issued2017
dc.date.updated2020-04-03T00:00:00Z
dc.description.abstractThe isoindolinone functionality and its derivatives are present in many naturally occurring and biologically active compounds. Tetrasubstituted isoindolinones such as 3, while a useful building block in materials as well as natural product synthesis, are particularly challenging to make. Current methods to make tetrasubstituted derivatives often require harsh conditions and expensive catalysts. Therefore, we decided to investigate a one-pot synthesis of this functional group using 5-exo-dig cyclization. Our strategy involved the intramolecular cyclization of alkynylbenzamide 1 using anhydrous conditions and trapping intermediate 2 with an electrophile. Several variables were investigated such as solvent, time, temperature, and identity of electrophile. Although the reactivity of intermediate 2 limited our choice with respect to solvents and electrophiles, we were successfully able to obtain target product 3 under certain conditions. Optimization and scope of the reaction will be discussed.
dc.description.copyright© Milhah Almansour, 2017
dc.description.noteImage of chemical compound embedded in abstract. Electronic and print versions available.
dc.description.noteM.Sc. University of New Brunswick, Department of Chemistry, 2017.
dc.formattext/xml
dc.format.extentxi, 58 pages ; illustrations
dc.format.mediumelectronic
dc.identifier.oclc(OCoLC)1148366900
dc.identifier.otherThesis 9991
dc.identifier.urihttps://unbscholar.lib.unb.ca/handle/1882/14157
dc.language.isoen_CA
dc.publisherUniversity of New Brunswick
dc.rightshttp://purl.org/coar/access_right/c_abf2
dc.subject.disciplineChemistry
dc.subject.lcshIsoindole -- Synthesis.
dc.subject.lcshHeterocyclic compounds.
dc.subject.lcshOrganic compounds -- Synthesis.
dc.titleOne-pot synthesis of tetrasubstituted isoindolinones
dc.typemaster thesis
thesis.degree.disciplineChemistry
thesis.degree.fullnameMaster of Science
thesis.degree.grantorUniversity of New Brunswick
thesis.degree.levelmasters
thesis.degree.nameM.Sc.

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