Alternatives to [4+1] carbocyclic annulations
dc.contributor.author | Dossett, David Lawrence | en |
dc.contributor.department | Chemistry | en |
dc.date.accessioned | 2020-12-14T16:35:07Z | en |
dc.date.available | 2020-12-14T16:35:07Z | en |
dc.date.issued | 1986 | en |
dc.description.abstract | 6-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.degree | M.S. | en |
dc.format.extent | iv, 51 leaves | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.uri | http://hdl.handle.net/10919/101269 | en |
dc.language.iso | en | en |
dc.publisher | Virginia Polytechnic Institute and State University | en |
dc.relation.isformatof | OCLC# 15174475 | en |
dc.rights | In Copyright | en |
dc.rights.uri | http://rightsstatements.org/vocab/InC/1.0/ | en |
dc.subject.lcc | LD5655.V855 1986.D677 | en |
dc.subject.lcsh | Synthetic products | en |
dc.title | Alternatives to [4+1] carbocyclic annulations | en |
dc.type | Thesis | en |
dc.type.dcmitype | Text | en |
thesis.degree.discipline | Chemistry | en |
thesis.degree.grantor | Virginia Polytechnic Institute and State University | en |
thesis.degree.level | masters | en |
thesis.degree.name | M.S. | en |
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