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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Redox-active cyclophane host molecules for the inclusion of cationic and neutral guest species

Lacy, Stephen Michael January 1993 (has links)
No description available.
2

Condensations in the unsaturated gamma ketonic acid and unsaturated gamma diketone groups.

Sabowitz, Morris. January 1934 (has links)
Thesis (Ph. D.)--New York University. / eContent provider-neutral record in process. Description based on print version record. Bibliography: p. 35.
3

Condensations in the unsaturated gamma ketonic acid and unsaturated gamma diketone groups.

Sabowitz, Morris. January 1934 (has links)
Thesis (Ph. D.)--New York University. / Bibliography: p. 35.
4

Heat-transfer coefficients for film condensation of steam on an inclined cylinder

Garrett, Todd January 1960 (has links)
This thesis discusses an investigation of film condensation of steam on the outside surface of an inclined cylinder. The objectives of the investigation were (1) to obtain heat-transfer coefficients for steam condensing on an inclined cylinder, (2) to determine the effect of the angle of inclination of the cylinder on the condensing coefficient, and (3) to verify values of the coefficient obtained from an accompanying theoretical development. Experiments were conducted for steam condensing on a 12.45 in. length of the outside surface of a 3/4 in. diameter by 0.065 in. thick wall, water-cooled, copper tube. Condensing coefficients were obtained for inclinations to the horizontal from 0° to 90° at 15° intervals. It was found that these coefficients decreased in value as the angle of inclination increased from 0° to 90°. At the same time good agreement was obtained between the measured and theoretical coefficients. No single equation could be found which would correlate the results for all the inclinations tested, but general equations were obtained which apply for each of two zones. One zone included inclinations from 0° to 30°, the other inclinations from 45° to 90°. The zone from 30° to 45° requires more investigation before it can be satisfactorily correlated. / Applied Science, Faculty of / Mechanical Engineering, Department of / Graduate
5

Studies of the condensation products of ethyl 3-phenyl-2,3-dioxopropanoate with active methylene compounds

Moore, Frank Archer. January 1952 (has links)
Call number: LD2668 .T4 1952 M61 / Master of Science
6

Further studies on phenolic hexamethylenetetramine compounds

Harvey, Mortimer Thomas, January 1920 (has links)
Thesis (Ph. D.)--Columbia University, 1920. / Vita.
7

Studies on the phenol formaldehyde condensation

Edell, Gerard Munz, January 1932 (has links)
Thesis (Ph. D.)--Columbia University, 1932. / Vita. Bibliography: p. 31.
8

The Stobbe condensation the use of sodium hydride as the condensing agent /

Daub, Guido H., January 1949 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1949. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.
9

The reductive condensation of 2,5-disubstituted pyrroles

White, James David January 1961 (has links)
The problem initially presented was the structural elucidation of a compound obtained when 2,5-dimethylpyrrole was subjected to conditions of acidic reduction. Previous workers had assigned a molecular formula C₁₂H₁₇N to this product and a partial structure had been put forward based on the indolenine system. In the course of this work it was found that the compound obtained by these earlier workers was the result of a reductive self-condensation of 2,5-dimethylpyrrole, and Its structure was conclusively established as 1,3,4,7-tetramethylisoindoline. The methods used in the structural elucidation of this product included elemental analysis of its derivatives, measurement of its basicity and equivalent weight, infrared and ultraviolet spectroscopic evidence, oxidative degradation, and its proton magnetic resonance spectrum. Two related isoindolines were prepared by different routes. 2,4,7-trimethylisoindoline was synthesised by methods analogous to those already known, and the ultraviolet spectrum of its methiodide, when compared with that of the methiodide from 1,3,4,7-tetramethylisoindoline, reinforced the structural assignment of the latter. 1,3-diphenyl-4,7-dimethylisoindoline was obtained by the reductive condensation of acetonylacetone with 2,5-diphenylpyrrole (which did not undergo self-condensation). The favourable result of this reaction suggested that a similar condensation may have occurred to give the 1,3,4,7-tetramethylisoindoline and also admitted the possibility of a general synthesis of substituted isoindolines by this route. An attempt was made to resolve the mechanism of the 2,5-dimethylpyrrole condensation, for which either a Diels-Alder reaction or a ring-opening process may be postulated. The failure of the dimethylpyrrole to show dienic character, even in the presence of very strong dienophiles, together with positive evidence for ring-opening and ketone-pyrrole condensation argued forcibly for the latter mechanism. / Science, Faculty of / Chemistry, Department of / Graduate
10

Malononitriles and cyanoacetamides containing isoxazoles and isoxazolines

Moores, Lee C. 13 August 2011 (has links)
Isoxazoles and isoxazolines have been shown in the literature to be an important scaffold for pharmaceuticals and insecticides, as well as a source of synthetic versatility important to many syntheses. As a substitute for other aromatic rings, isoxazoles are known to change the efficacy of a given compound. Isoxazolines can be used as a precursor to many other functional moieties that may be effected during earlier synthetic steps. There are many routes to the heterocyclic moiety, allowing for their insertion in a wide range of molecules. Our group has previously reported a condensation of arylaldehydes with hydroxylamine to first make an aryloxime which can, after generating the nitrile oxide, then cyclize with an alkene or alkyne in situ and create the isoxazoline or isoxazole, respectively. The Knoevenagel Condensation reaction is identified as the addition of an activated methylene complex, malononitrile or cyanoacetamide, with a carbonyl followed by dehydration.. Our group has previously reported a facile, one-pot reductive alkylation of benzyl malononitriles. These compounds have been noted as having many insecticidal uses, as well as being potent pharmacophores. The scope of this project is to further explore and optimize the condensation of aryl aldehydes and methylene complexes. The condensed and reduced methylene complex will then be alkylated to join the heterocyclic moiety to reach the final disubstituted methylene product. A second approach will also be explored in which the monosubstituted malononitrile will first be alkylated with allyl or propargyl bromide, which can then undergo a 1,3-dipolar cycloaddition with a nitrile oxide. The library of compounds generated will be sent to collaborators to test the biological activity of the molecules. / Introduction and background literature -- Reactions of methylene complexes -- Synthesis of disubstituted methylene complexes. / Department of Chemistry

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