Welcome to the upgraded MacSphere! We're putting the finishing touches on it; if you notice anything amiss, email macsphere@mcmaster.ca

Studies on the Structure of Lycopodine

dc.contributor.advisorMacLean, D. B.
dc.contributor.authorHarrison, William Ashley
dc.contributor.departmentChemistryen_US
dc.date.accessioned2024-06-17T21:41:07Z
dc.date.available2024-06-17T21:41:07Z
dc.date.issued1957-04
dc.description.abstractThe ring opened in the formation of α-cyanobromolycopodine has been found to be six-membered or larger. The product of hydrogenation of β-cyanobromolycopodine in alkaline medium has been shown to be the cyclized compound, C17H24ON2, not β-cyanolycopodine, C17H26ON2, as thought previously. A study was made of the β-cyclized compound but it could not be ascertained whether it has a ketone or an enol-ether structure. The possibility of a β-piperidone structure for lycopodine is discusseden_US
dc.description.degreeMaster of Science (MS)en_US
dc.description.degreetypeThesisen_US
dc.identifier.urihttp://hdl.handle.net/11375/29868
dc.language.isoenen_US
dc.subjectlycopodineen_US
dc.subjectchemistryen_US
dc.subjectstructureen_US
dc.subjectformationen_US
dc.titleStudies on the Structure of Lycopodineen_US
dc.typeThesisen_US

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Harrison_William_1957Apr_Masters.pdf
Size:
2.37 MB
Format:
Adobe Portable Document Format

License bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
1.68 KB
Format:
Item-specific license agreed upon to submission
Description: