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The metabolism of creatine in guinea pigs

Creator:: Hardie, Waldo Richard
Resource Type:: Masters Thesis
Full Text:: creatine. THE I.IETABOLISM OF CREATINE IN GUINEA PIGS by RICHARD HARDIE A THESIS submitted to

A cerometric method of determining sulfates

Creator:: Johnson, Karl Richard
Resource Type:: Masters Thesis
Full Text:: OF DETERMINING SULFATES by KARL RICHARD JORNSON A THESIS submitteJ to the OREGON STATE

A study of the preparation of amylene chlorohydrin

Creator:: Biggerstaff, Warren Richard
Resource Type:: Masters Thesis
Full Text:: for privacy (J t Professor of Organic ChentLstry In Charge of Major Redacted for privacy c

Siloxy-cope rearrangements of the trans-l-vinylcyclotridec-3-en-l-ol system

Creator:: Bolesta, Richard Edward
Abstract:: The thermolysis of trans-1 -trimethylsiloxy- 1-vinylcyclotridec- 3-ene (VI-OTMS) led to the formation of two major products: 4-vinylcyclotridecanone (VII) and cyclopentadec-5-en-l-one (VIII) after hydrolysis. Ketone VII is produced by a concerted [3, 3] sigmatropic shift, while ketone VIII is formed by a [1, 3] sigmatropic shift with a concerted or diradical...
Resource Type:: Masters Thesis
Full Text:: AN ABSTRACT OF THE THESIS OF RICHARD EDWARD BOLESTA for the

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

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:: ACKNOWLEDGEMENTS I would like to gratefully acknowledge my major professor, Dr. Richard W. Thies, and Dr. Terry J

The siloxy-cope rearrangement of 1,2-divinyl-1-trimethyl-siloxycyclohexane and related systems. The acid-catalyzed rearrangement of bicyclo [5.1.0] octyl-8-methanol

Creator:: Walton, Edward Samuel
Abstract:: Part I The pyrolysis of cis- and trans- 1, 2-divinyl-1- trimethylsiloxy - cyclohexane, II- and III-TMS, under the same conditions as the pyrolysis of cis-l-vinyl -1-trimethylsiloxycyclooct-3-ene, I-TMS, confirms that a sequence of concerted reactions for the rearrangement of II- and III-TMS to trans-l-trimethylsiloxycyclodec-3-ene, IV-TMS, is a viable pathway in the...
Resource Type:: Masters Thesis
Full Text:: approved: Part I Redacted for Privacy Dr. Richard W. Thies The pyrolysis of cis- and trans- 1, 2-divinyl

Ring expansion 3-methoxy-6-vinyl-7,8,9,10-tetrahydro-6(5H)-benzocyclooctenol

Creator:: Meshgini, Mehdi
Resource Type:: Masters Thesis
Full Text:: )-BENZOCYCLOOCTENOL Abstract approved: Redacted for Privacy Dr. Richard W. Thies The potassium salts of 6- vinyl -7

Catalytic rearrangement of cyclodeca-1,2,5-triene and oxymercuration of bicyclo-[7.1.0]-deca-2,3-diene

Creator:: Boop, Janice Lee
Abstract:: The reaction of cyclodeca-1,215triene with mercuric salts gave only rearranged hydrocarbon, tricyclo[4.4.0.0²'⁴]deca-5ene in acetic acid. Other catalysts [Rh(CO)₂C1]₂ and AgC10₄ gave the same rearranged hydrocarbon. The isomerization is proposed to proceed through a "metalcomplexed" carbenoid intermediate. The reaction of bicyclo[7.1.0 ]deca-213diene gave oxymercurated products.
Resource Type:: Masters Thesis
Full Text:: for Privacy Dr. Richard W. Thies The reaction of cyclodeca-1,215triene with mercuric salts gave

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

The metabolism of creatine in guinea pigs

A cerometric method of determining sulfates

A study of the preparation of amylene chlorohydrin

Siloxy-cope rearrangements of the trans-l-vinylcyclotridec-3-en-l-ol system

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

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

The siloxy-cope rearrangement of 1,2-divinyl-1-trimethyl-siloxycyclohexane and related systems. The acid-catalyzed rearrangement of bicyclo [5.1.0] octyl-8-methanol

Ring expansion 3-methoxy-6-vinyl-7,8,9,10-tetrahydro-6(5H)-benzocyclooctenol

Catalytic rearrangement of cyclodeca-1,2,5-triene and oxymercuration of bicyclo-[7.1.0]-deca-2,3-diene

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

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