Alternatives to [4+1] carbocyclic annulations

dc.contributor.authorDossett, David Lawrenceen
dc.contributor.departmentChemistryen
dc.date.accessioned2020-12-14T16:35:07Zen
dc.date.available2020-12-14T16:35:07Zen
dc.date.issued1986en
dc.description.abstract6-Carboethoxybicyclo [3.3.0] oct-6-en-2-one has been prepared by the intramolecular [4+1] cyclopentene annulation method. This compound and its precursor, 6-vinyl-6-carboethoxybicyclo[3.1.0]hexan-2-one were attained as the necessary standards for the investigation of the course of intramolecular Michael addition-alkylation sequence of l-phenylsulfonyl-6-carboethoxyocta-5,7-dien-2-one.en
dc.description.degreeM.S.en
dc.format.extentiv, 51 leavesen
dc.format.mimetypeapplication/pdfen
dc.identifier.urihttp://hdl.handle.net/10919/101269en
dc.language.isoenen
dc.publisherVirginia Polytechnic Institute and State Universityen
dc.relation.isformatofOCLC# 15174475en
dc.rightsIn Copyrighten
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/en
dc.subject.lccLD5655.V855 1986.D677en
dc.subject.lcshSynthetic productsen
dc.titleAlternatives to [4+1] carbocyclic annulationsen
dc.typeThesisen
dc.type.dcmitypeTexten
thesis.degree.disciplineChemistryen
thesis.degree.grantorVirginia Polytechnic Institute and State Universityen
thesis.degree.levelmastersen
thesis.degree.nameM.S.en

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