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Synthesis of large-ring analogs of estrone

Creator:: Pierce, John Robert
Resource Type:: Dissertation
Full Text:: THE THESIS OF John Robert Pierce for the degree of Doctor of Philosophy in Chemistr presented on

The thermal decomposition of aralkyl thiocarbonates

Creator:: Bartsch, Richard A.
Resource Type:: Masters Thesis
Full Text:: AN ABSTRACT RICHARD ALLEN BARTSCH OF THE THESIS OF for

Beginning the search for the inverse fission of uranium

Creator:: Beckerman, John R.
Abstract:: The nuclear reaction ¹⁰⁰Mo(¹²⁴Sn,xn)[superscript 224-x]U has been carried out at E[subscript cot] of 578 MeV and 634 MeV using the facilities and equipment at the Holifield Radioactive Ion Beam Facility (HRIBF) at Oak Ridge National Laboratory (ORNL) in order to initiate the search for the inverse fission of uranium. Reference...
Resource Type:: Masters Thesis
Full Text:: John R. Beckerman for the degree of Master of Science in Chemistry presented on June 9, 2010

Oxymercuration of cyclodeca-1,2,5,8-tetraene

Creator:: Hong, Pak-Kong
Abstract:: The reactions of cyclodeca-1, 2, 5, 8-tetraene with mercuric salts in solvents of varying nucleophilicity are described. Instead of forming the usual oxymercuration products reported for reactions of olefins and allenes with mercuric salts, the major products obtained in the present cases result from the initial electrophilic addition of the...
Resource Type:: Masters Thesis
Full Text:: CYCLODECA-1, 2, 5, 8-TETRAENE Abstract approved: Redacted for privacy Dr. Richard W. Thies The reactions

Exploratory studies directed toward the synthesis of large ring hormone analogs

Creator:: Chiarello, Ronald Harry
Resource Type:: Dissertation
Full Text:: TOWARD THE SYNTHESIS OF LARGE RING HORMONE ANALOGS Abstract approved: Redacted for privacy Richard W

Ring expansion reactions of alkoxides and their application toward synthesis of large ring hormone models

Creator:: Seitz, Earl Philip
Abstract:: The potassium salts of a series of 1-vinylcycloalk-3-en-l-ols were found to undergo ring expanding [1, 3]-sigmatropic shifts at 25° when dissolved in hexamethylphosphoramide (HMPA) or 1, 2-dimethoxyethane (DME) with 18-crown-6. The yields and reaction rates were compared with those of the corresponding Siloxy-Cope ring expansions. These anionic cases showed about...
Resource Type:: Dissertation
Full Text:: Redacted for privacyAbstract approved: Richard W. Thies The potassium salts of a series of 1-vinylcycloalk

Oxy-Cope, and Siloxy-Cope rearrangement of cis-1-vinylcyclooct-3-en-1-ol

Creator:: Chin, Alice Wai-lee
Abstract:: Both oxy-Cope and siloxy-Cope rearrangements involve (1, 3) and (3, 3) sigrnatropic shifts. Both the concerted mechanism, and the stepwise mechanism via a diradical intermediate are possible. In a cyclic system such as cis-l-vinylcyclooct-3-en-l-ol, the thermal rearrangement takes place preferably through a diradical intermediate. At high temperature, the reaction also...
Resource Type:: Masters Thesis
Full Text:: Rearrangement of cis-l-vinyl- cyclooc t-3 -en -I .ol, Abstract approved: Redacted for Privacy Dr. Richard W

Exploratory studies of the mechanism of 1,3 sigmatropic ring expansion reactions

Creator:: James, Corinne Patricia
Abstract:: The potassium salts of certain 1-vinylcycloalk-3-en-l-ols have been found to undergo sigmatropic ring expansion rearrangements in HMPA. Preliminary investigations of several benzo-substituted medium ring systems were undertaken in order to determine which of these was best suited for further study. A synthetic sequence leading to the formation of 5-methy1-6-viny1-7,8,9,10-tetrahydro-6-benzocyclo-octenol, which...
Resource Type:: Masters Thesis
Full Text:: Sigmatropic Ring Expansion Reactions Abstract approved: Redacted for Privacy Richard W. Thies The potassium

The photodecomposition of t-butyl bicyclo [7.1.0] decane-2-percarboxylate

Creator:: McRitchie, Donna Louise
Abstract:: This paper describes the synthesis of t-butyl bicyclo[7.1.0] decane-2-percarboxylate and its photolytic decomposition. The title compound was found to undergo simple homolytic cleavage when exposed to light of 2537 A; producing the cyclodecyl radical, carbon dioxide, and t-butoxy radical. The largest percentage of products arose from an intimate radical pair...
Resource Type:: Masters Thesis
Full Text:: Abstract approved: Redacted for Privacy Richard W. Thies This paper describes the synthesis of t-butyl

A pyrolysis of cis-1-trimethylsiloxy-1-cyclopropyl-3-cyclononene : the thermal isomerization of 2-phenyl-1-trimethylsiloxy-1-vinylcyclononane

Creator:: Choi, Young Bok
Abstract:: Part 1 The pyrolysis of cis-1-trimethylsiloxy-1-cyclopr opyl-3-cyclononene in the temperature range 285-350° is described. Instead of siloxy-Cope rearrangement, undesired desiloxylation took place. Part 2 Gas-phase pyrolytic rearrangement of 2-phenyl-1-trimethylsiloxy-1-vinylcyclononane was investigated in a static system in the temperature range 213-330°. It was discovered that three major products resulted: cis- and...
Resource Type:: Masters Thesis
Full Text:: Redacted for privacy Dr. Richard W. Thies The pyrolysis of cis -1 tr imethyls iloxy- 1 - cyclopr opyl- 3

ScholarsArchive@OSU

Synthesis of large-ring analogs of estrone

The thermal decomposition of aralkyl thiocarbonates

Beginning the search for the inverse fission of uranium

Oxymercuration of cyclodeca-1,2,5,8-tetraene

Exploratory studies directed toward the synthesis of large ring hormone analogs

Ring expansion reactions of alkoxides and their application toward synthesis of large ring hormone models

Oxy-Cope, and Siloxy-Cope rearrangement of cis-1-vinylcyclooct-3-en-1-ol

Exploratory studies of the mechanism of 1,3 sigmatropic ring expansion reactions

The photodecomposition of t-butyl bicyclo [7.1.0] decane-2-percarboxylate

A pyrolysis of cis-1-trimethylsiloxy-1-cyclopropyl-3-cyclononene : the thermal isomerization of 2-phenyl-1-trimethylsiloxy-1-vinylcyclononane

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