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Nitrogen Derivatives of Naphthoquinone

Description: A series of nitrogen derivatives of 1,4-naphthoquinone, which are structurally similar to the compounds of Hall, has been prepared by this worker. In general, the amido groups are those of the long-chain, fatty acids, and it is believed they will have increased physiological activity. These compounds are to be tested for medicinal activity by Parke-Davis and Company.
Date: June 1953
Creator: Wood, Frank M.
Item Type: Refine your search to only Thesis or Dissertation
Partner: UNT Libraries
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Synthesis of some 1-Substituted-2-Methylnaphthimidazole-4,9-Diones

Description: Imidazole derivatives of 1,4-naphthoquinones are found to have biological activity which interferes with the utilization of vitamin K or of the purines since they have groups common to these two classes of compounds. This thesis shows the preparation of some 1-substituted-naphthimidazole-4,9-diones for possible biological activity.
Date: August 1957
Creator: Peterson, Harold W.
Item Type: Refine your search to only Thesis or Dissertation
Partner: UNT Libraries
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A Study of the Friedel-Craft Reactions of Phenolic Ethers

Description: The original purpose of this investigation was to prepare a series of diketones. However, since considerable difficulty was encountered in the preparation of these diketones, attention was shifted to a study of the Friedel-Craft reactions of phenolic ethers and to the reaction between phenolic ethers and dicarboxylic acids with boron trifluoride as a catalyst.
Date: January 1959
Creator: Roberson, Charles Ray
Item Type: Refine your search to only Thesis or Dissertation
Partner: UNT Libraries
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Some Amine Derivatives of 1,4-naphthoquinone

Description: It was the aim of this investigation to prepare derivatives of 1,4-naphthoquinone substituted at the 2- and 3- positions with various amino groups. 2,3-Dichloro-1,4-naphthoquinone was selected as the starting material because of the possibility of replacing the chloro groups in direct substitution reactions with amines.
Date: August 1959
Creator: Cunningham, Robert Gipson
Item Type: Refine your search to only Thesis or Dissertation
Partner: UNT Libraries
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Naphthoquinone Studies

Description: This thesis describes a series of naphthoquinone reactions employing pyridine carboxylic acid derivatives (nicotinic acid derivatives). The products of these reactions will be tested by Parke, Davis and Company for their activity against the tubercle bacillus and other pathogenic microorganisms.
Date: 1955
Creator: Padgett, William A.
Item Type: Refine your search to only Thesis or Dissertation
Partner: UNT Libraries
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Nitration of Thiophene Analogs of DDT

Description: Since thiophene very often yields compounds that are analogous to benzene derivatives in general physiological properties, it was decided to attempt to prepare the nitro and amino derivatives of 1,1,1-trichloro-2,2-bis-(2-thienyl)-ethane (V) as well as the nitro and amino derivatives of 2,2,3-trichloro-1,1-bis-(2-thienyl)-butane (VI).
Date: February 1953
Creator: Buttram, Jack Rhea
Item Type: Refine your search to only Thesis or Dissertation
Partner: UNT Libraries
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Naphth [2,3-d] Imidazoline-2,4,9-Triones

Description: The study of some acylurea derivatives of 2-amino-3-alkylamino- and -3-arylamino-1,4-naphthoquinones was undertaken to determine the course of reaction under conditions similar to those used by J. R. Hoover and A. R. Day to prepare 2-alkyl-1H-naphth[2,3-d] imidazole-4.9-diones from 2-acylamino-3-amino-1,4-naphthoquinones.
Date: August 1966
Creator: Witkowski, Joseph T.
Item Type: Refine your search to only Thesis or Dissertation
Partner: UNT Libraries
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Stereochemical Elucidation Of The Tetrahydro [2.2]paracyclophane System

Description: The purpose of this investigation is to study the Birch reduction products of [2.2lparacyclophane and of [2.2]paracyclophane- 2-carboxylic acid. The tetrahydro Birch reduction product of [2.2]paracyclophane is shown to be dl stereoisomer, with the olefins of the upper deck only partially overlapping with the olefins of the lower deck. This stereochemical elucidation is accomplished by means of a complete proton nmr analysis of the tetraepoxide derivative. A proposed mechanism supported by VB (v… more
Date: August 1975
Creator: Song, Ban-Huat
Item Type: Refine your search to only Thesis or Dissertation
Partner: UNT Libraries
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