Synthesis of some compounds of possible carcinogenic activity

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dc.contributor.authorBorkovec, Alexej B.en
dc.contributor.committeechairVingiello, Frank A.en
dc.contributor.committeememberMurray, John W.en
dc.contributor.committeememberKing, Kendall W.en
dc.contributor.departmentChemistryen
dc.date.accessioned2014-03-14T21:08:45Zen
dc.date.adate2010-01-12en
dc.date.available2014-03-14T21:08:45Zen
dc.date.issued1955-06-03en
dc.date.rdate2010-01-12en
dc.date.sdate2010-01-12en
dc.description.abstract1. The acid catalyzed cyclodehydration method was extended to the 9-aryl-1,2-benzanthracene and 9-naphthylanthracene series. 2. A new method of cyeclodehydration was described. 3. The series of 10-mono- and 10-dimethylphenyl-1,2-benzanthracenes was completed. All the isomeric 9-mono- and 9-dimethylphenyl-1,2-benzanthracenes were prepared together with the corresponding ketones. Some highly hindered ketones were prepared and their cyclization realized. A total of 47 compounds, not previously reported in the literature, were synthesized. 4. The spectra of 24 hydrocarbons were recorded and the theory of nonplanarity of these compounds substantiated.en
dc.description.degreePh. D.en
dc.format.extent145 leavesen
dc.format.mediumBTDen
dc.format.mimetypeapplication/pdfen
dc.identifier.otheretd-01122010-020226en
dc.identifier.sourceurlhttp://scholar.lib.vt.edu/theses/available/etd-01122010-020226/en
dc.identifier.urihttp://hdl.handle.net/10919/37187en
dc.language.isoenen
dc.publisherVirginia Techen
dc.relation.haspartLD5655.V856_1955.B674.pdfen
dc.relation.isformatofOCLC# 20499636en
dc.rightsIn Copyrighten
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/en
dc.subject.lccLD5655.V856 1955.B674en
dc.subject.lcshCancer -- Researchen
dc.subject.lcshCarcinogenicity testingen
dc.titleSynthesis of some compounds of possible carcinogenic activityen
dc.typeDissertationen
dc.type.dcmitypeTexten
thesis.degree.disciplineChemistryen
thesis.degree.grantorVirginia Polytechnic Instituteen
thesis.degree.leveldoctoralen
thesis.degree.namePh. D.en

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