New methods for the preparation of vicinal diamines and monoamines from olefins and cyanamide

dc.contributor.advisorKohn, Harold Lewis
dc.contributor.committeeMemberAlbright, Thomas A.
dc.contributor.committeeMemberGeanangel, Russell A.
dc.contributor.committeeMemberLemke, Thomas L.
dc.contributor.committeeMemberThummel, Randolph Paul
dc.creatorJung, Sang-Hun
dc.date.accessioned2023-12-13T20:52:52Z
dc.date.available2023-12-13T20:52:52Z
dc.date.issued1984
dc.description.abstractTwo new vicinal diamination procedures have been developed beginning with unactivated alkenes 49 and cyanamide (50). These methods are marked by their simplicity and cost-efficiency. Moreover, these techniques proceeded Stereospecifically and permitted access to nitrogen unsubstituted diamines. Most alkenes 49 utilized in this study yielded the key bromocyanamide intermediates 52 upon treatment with cyanamide (50) and N-bromo- Succinimide (51). Bromocyanamides 52 were then converted to the vicinal diamines 1 in one of two ways. In a Solvolytic approach, condensation of cyanamides 52 with ethanol in the presence of anhydrous hydrochloric acid gave the corresponding protonated isourea salts 53. Treatment 53 with mild bases (triethyl amine, sodium bicarbonate) in select cases yielded imidazolines 57. Alternatively, use of strongly basic conditions (sodium ethoxide or sodium hydroxide) led to the predominant formation of aziridines 55. These aziridines could be converted to imidazolines 57 with various nucleophilic catalysts. The scope of this isomerization was examined. Basic hydrolysis of the imidazolines 57 in the final step yielded the desired vicinal diamines 1 in 47-71% overall yield. [...]
dc.description.departmentChemistry, Department of
dc.format.digitalOriginreformatted digital
dc.format.mimetypeapplication/pdf
dc.identifier.other11382682
dc.identifier.urihttps://hdl.handle.net/10657/15628
dc.language.isoen
dc.rightsThis item is protected by copyright but is made available here under a claim of fair use (17 U.S.C. Section 107) for non-profit research and educational purposes. Users of this work assume the responsibility for determining copyright status prior to reusing, publishing, or reproducing this item for purposes other than what is allowed by fair use or other copyright exemptions. Any reuse of this item in excess of fair use or other copyright exemptions requires express permission of the copyright holder.
dc.subjectOrganic compounds--Synthesis
dc.subjectPolyamines
dc.subjectAmines
dc.titleNew methods for the preparation of vicinal diamines and monoamines from olefins and cyanamide
dc.type.dcmiText
dc.type.genreThesis
thesis.degree.collegeCollege of Natural Sciences and Mathematics
thesis.degree.departmentChemistry, Department of
thesis.degree.disciplineChemistry
thesis.degree.grantorUniversity of Houston
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy

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