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The Chemistry Of Dehydronaphthalene, Richard Harold Hales Aug 1970

The Chemistry Of Dehydronaphthalene, Richard Harold Hales

Theses and Dissertations

The reaction of monohalonaphthalenes with potassium t-butoxide in a t-butyl alcohol-dimethyl sulfoxide (DMSO) mixture has been studied. The 1-bromonaphthalene reaction was extensively studied. Fifteen identifiable products were observed and conditions were found where the desired products, 1- and 2-t-butyl naphthyl ethers (V and VI) were formed in maximum yield, and their decomposition products, 1- and 2-naphthol (XIV and XV), were formed in minimum yield. The mole percent ratio of 1-substituted products (V and XIV) to 2-substituted products (VI and XV) was found under standardized conditions to be 0.35 ± 0.03 in every case when the halogen was I, Br and …


The Effects Of Various Treatments On Thiamin Diphosphate And Total Thiamin Levels Of Rat Tissues, Dong Hwa Park Aug 1970

The Effects Of Various Treatments On Thiamin Diphosphate And Total Thiamin Levels Of Rat Tissues, Dong Hwa Park

Theses and Dissertations

Tissue thiamin diphosphate was assayed enzymatically utilizing purified brewer's yeast apotransketolase. With this assay ten uumoles of thiamin diphosphate could be detected. Total thiamin was fluorometrically measured. For one to three days rats were placed under conditions of stress, consisting of loud noise treatment, emotional stress, deprivation of paradoxical sleep, and swimming to exhaustion, respectively. The body weight was markedly decreased at the end of the respective experimental periods except with the loud noise treated group, compared with the corresponding controls. Following two to three such consecutive treatments, the adrenal weight also showed a significant increase. Thiamin diphosphate and total …


Preparation Of New Amino-, Thio-, And Sulfonyladamantane Derivatives, Joseph Craig Argyle Jun 1970

Preparation Of New Amino-, Thio-, And Sulfonyladamantane Derivatives, Joseph Craig Argyle

Theses and Dissertations

Various synthetic schemes were used to prepare a number of new amino-thio- and sulfonyladamantane compounds. By a nucleophilic substitution on 1-bromoadamantane, 1-(p-nitrophenylthio)adamantane was prepared from p-nitrothiophenol; the amino- and sulfonyl- derivatives of this compound were also prepared. Silver tosylate was used to generate the 1-adamantyl carbonium ion from 1-bromoadamantane in a synthetically useful procedure for preparing 1-adamantylamides from nitriles. Three 1-(1-adamantylcarbinyl)-2,5-dialkylpyrroles were prepared by Knorr-Paal reactions and reduced to the corresponding pyrrolidines. Thio- and aminomethyl 1-adamantyl ketones were prepared from methyl and bromomethyl 1-adamantyl ketones, respectively. Aliphatic and aromatic oxiranes were reacted with 1-aminoadamantane in a bomb at elevated temperatures …


The Synthesis And Properties Of New Potentially Chemotheraputic [Sic] Pteridine Derivatives, Walter Wesley Parish Jun 1970

The Synthesis And Properties Of New Potentially Chemotheraputic [Sic] Pteridine Derivatives, Walter Wesley Parish

Theses and Dissertations

A new general synthetic method for the preparation of 6-thiopteridines has been developed. The method involves the addition of thiols to intermediate pyrimidine nitrones formed in situ by the reaction of 4-amino-5-nitrosopyrimidines with pyridinium-activated acetonitriles, acetates, acetophenones, and other methylketones. Ca. forty new pteridines were prepared by this method. The preparation of six new 6-pteridinyl ketones, two new 6- pteridinyl ketone thiosemicarbazones, and two new 6-sulfonylpteridines and their 4-acetamido derivatives is also reported. 4-Acetamido-2- amino-7-phenylpteridine 5-oxide was prepared by the reaction of 2- amino-4,6-diacetamido-5-nitrosopyrimidine with either phenylsulfonyl-acetophenone or phenacylpyridinium bromide. Evidence relating to the structure of the acylated 4-amino-5- nitrosopyrimidines …


The Reactivity And Selectivity Of The Reaction Of Sulfur Trioxide And Bromobenzene, Sullivan E. Blau Jun 1970

The Reactivity And Selectivity Of The Reaction Of Sulfur Trioxide And Bromobenzene, Sullivan E. Blau

Theses and Dissertations

The sulfonation of bromobenzene with sulfur trioxide in liquid sulfur dioxide at -12 to -13° C. was studied to determine its relative reactivity. The relative rate constant ratio, kbenzene/kbromobenzene, was found to be 28.6 in a competitive reaction between benzene and bromobenzene. The isomer distribution was found to be 0.15 ± 0.02% for the meta, 0.91 ± 0.04% for the ortho and 98.93 ± 0.14% for the para isomers. The partial rate factors were calculated to be pf= 0.208, of= 0.0096 and mf = 0.00018. The relative rate data exhibited a distinctive behaviour previously noted in related systems, possibly due …


High Pressure Spectral Chemistry Of Selected Organic Compounds, Frank William Linsley Jun 1970

High Pressure Spectral Chemistry Of Selected Organic Compounds, Frank William Linsley

Theses and Dissertations

The series of compounds indicated by the formular C_6H_5-(CH=CH)n-C_6H_5 change in color from white (colorless) to yellow to orange to red to deep red as n increases from 1 to 12. Stilbene is the first compound of this series (n=1). Under pressure, exerted by a diamond anvil press, stilbene can be seen to change color from white to yellow to red as increasing pressure is applied. Similar color changes are observed for the compounds where n=2,3, and 4 when subjected to similar pressure. This study records and reports the spectra versus pressure for these compounds.


Donor Properties Of Dimethylsulfoniumcyclopentadienylide And Tetramethylenesulfoniumcyclopentadienylide In Metal Complexes ; Part Ii. The Attempted Preparation Of Boron Tricyanide, Gary Scott Barney May 1970

Donor Properties Of Dimethylsulfoniumcyclopentadienylide And Tetramethylenesulfoniumcyclopentadienylide In Metal Complexes ; Part Ii. The Attempted Preparation Of Boron Tricyanide, Gary Scott Barney

Theses and Dissertations

Part I.--Complexes of dimethylsulfoniumcyclopentadientylide and tetramethylenesulfoniumcyclopentadienylide with metal ions were studied in order to determine the coordination site on the ylids. Infrared spectra indicate that the ylids are coordinated through the cyclopentadienyl ring in all complexes except for the Hg(CN)2 complexes. Coordination-of the HgI2, CdI2, ZnCl2, and AgNO3 complexes is through the number one position on the ring as suggested by NMR data. Infrared and NMR data strongly indicate that the ylids in the Hg(CN)2 complexes are coordinated through sulfur. Part II.--The only method given in the chemical literature for the preparation of boron tricyanide could not be duplicated in …