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Filtering by: Academic Affiliation Chemistry Remove constraint Academic Affiliation: Chemistry Advisor Marvell, Elliot N. Remove constraint Advisor: Marvell, Elliot N. Rights Statement Copyright Not Evaluated Remove constraint Rights Statement: Copyright Not Evaluated

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Thermolysis of cis,cis,trans-1-phenyl-1,3,5-heptatriene

Creator:

Tilton, Mary Lehman

Abstract:

Isomerically pure cis,cis,trans-1-pheny1-1,3,5- heptatriene was prepared and cyclized. Ring closure was followed by a 1,5 hydrogen shift, and the only product observed was 1-phenyl -6-methyl -1,3-cyclohexadiene. Rough first order rate constants for thermolysis and the hydrogen shift were determined. Kinetic estimates indicate that the report of disallowed product in a...

Resource Type:

Masters Thesis
Approaches to the synthesis of botryococcene : synthesis of the half molecule

Creator:

Strycker, Arden R.

Resource Type:

Dissertation
Syntheses via thermal rearrangements : a new route to 4-cycloheptenones and approaches to medium rings

Creator:

Titterington, Donald Roy

Resource Type:

Dissertation
The aromatic Cope rearrangement : energetics and reality

Creator:

Almond, Stephen W.

Resource Type:

Dissertation
Thermal reactions of some selected olefins

Creator:

Moy, Gerald George

Resource Type:

Dissertation
1,2-divinylcyclohexenes : synthesis and thermal rearrangement studies

Creator:

Delphey, Craig Edward

Resource Type:

Dissertation
The retro-ene reaction of 2-vinylcyclohexanols and approaches to the synthesis of botryococcene

Creator:

Rusay, Ronald Joseph

Abstract:

The retro-ene reaction of 2-vinylcyclohexanols occurs readily in the vapor phase at 400-450° producing unsaturated carbonyl compounds in good yields. The starting- materials were prepared in general by the carbenoid addition reaction of ethyl diazoacetate, appropriately substituted cyclohexene, and copper catalyst to produce bicyclic esters which were reduced to the...

Resource Type:

Dissertation
The intramolecular ene reaction of some 1,2-diallylcyclohexanes

Creator:

Cheng, Jack Ching-Ping

Abstract:

The familiar equilibrium between 1, 7- octadiene and cyclooctene at temperatures exceeding 3000, indicates that an ene-retroene process could be used as a six atom ring expansion method. To test this possibility we prepared both cis and trans isomers of 1, 2- diallyl- 1, 2 -bis (trimethylsiloxy) cyclohexane and pyrolyzed...

Resource Type:

Masters Thesis
Part I.: Reactions of 2-isopropoxymethylene-cyclohexanone with organometallic reagents. Part II.: Thermal rearrangements of ethyl 3-(2-vinylcyclohexen-1-y1) propenoate and 1-vinyl-2-propenylidenecyclohexyl methyl ether

Creator:

Cleary, Michael Franklin

Resource Type:

Dissertation
Concerted dearomatization reactions : cis-1-phenyl-2-vinylcyclopropane in the Cope rearrangement

Creator:

Lin, Crystal

Resource Type:

Dissertation

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Academic Affiliation

Chemistry[remove]44

Advisor

Marvell, Elliot N.[remove]44

Commencement Year

Commencement Year range begin – Commencement Year range end

Current results range from 1950 to 1982

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Creator

Stephenson, John Louis2
Almond, Stephen W.1
Anderson, Daniel Richard1
Chadwick, Thomas Carl, 1945 1
Cheng, Jack Ching Ping1
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Date

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Current results range from 1950 to 1981

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1980-19893
1970-197911
1960-196919
1950-195911

Degree Field

Chemistry44

Degree Level

Doctoral27
Master's17

Degree Name

Doctor of Philosophy (Ph.D.)27
Master of Science (M.S.)17

Language

English [eng]44

Non-Academic Affiliation

Oregon State University. Graduate School44

Peer Reviewed

No44

Resource Type

Dissertation27
Masters Thesis17

Rights Statement

Copyright Not Evaluated[remove]44

Subject

Chemical reactions7
Claisen condensation4
Organic compounds -- Synthesis4
Rearrangements (Chemistry)4
Ethers3
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