Stereochemical studies of the C.1 methyl group in the trans-1-methyl-2, 8-dioxo-decahydronaphthalene systems

dc.contributor.advisorTurner, Richard B.
dc.creatorMiller, Russell Bryan
dc.date.accessioned2007-05-09T18:40:35Z
dc.date.available2007-05-09T18:40:35Z
dc.date.issued1967
dc.description.abstractA study was carried cut to determine the relative stereochemistry of the thermodynamically most stable isomer of the l-methyl-2,8-dioxodecahydronaphthalene system. This study was prompted by an apparent ambiguity in the stereochemical assignment of the C.
dc.format.digitalOriginreformatted digital
dc.format.extent83 pp
dc.format.mimetypeapplication/pdf
dc.identifier.callnoThesis Chem. 1967 Miller
dc.identifier.citationMiller, Russell Bryan. "Stereochemical studies of the C.1 methyl group in the trans-1-methyl-2, 8-dioxo-decahydronaphthalene systems." (1967) Diss., Rice University. <a href="https://hdl.handle.net/1911/14384">https://hdl.handle.net/1911/14384</a>.
dc.identifier.digitalRICE0003
dc.identifier.urihttps://hdl.handle.net/1911/14384
dc.language.isoeng
dc.rightsCopyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.
dc.subjectOrganic chemistry
dc.titleStereochemical studies of the C.1 methyl group in the trans-1-methyl-2, 8-dioxo-decahydronaphthalene systems
dc.typeThesis
dc.type.materialText
thesis.degree.departmentChemistry
thesis.degree.disciplineNatural Sciences
thesis.degree.grantorRice University
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
RICE0003.pdf
Size:
1.85 MB
Format:
Adobe Portable Document Format
Description: