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Synthetic studies on marine natural products : I. Stereoselective synthesis of E,Z-1,3-Dienes by tandem nucleophilic addition to a dienylphosphonium salt followed by Wittig reaction. II. Synthesis of cyclopropyl oxylipins by a cation mediated carbocyclization

Creator:: Jensen, Mark S.
Resource Type:: Dissertation
Full Text:: approved: James D. White I. A new stereoselective route for the synthesis of E,Z-1,3-dienes using a

The nature of the chemical constituents of incense cedar, Libocedrus decurrens (Torr.) bark

Creator:: Smith, James E. (James Edward)
Abstract:: The purpose of this investigation was to determine the nature of the chemical constituents of incense cedar bark with the hope that such an endeavor would spur future research, development and use of a now neglected natural raw material. The bark from nine trees, which were separated into three age...
Resource Type:: Masters Thesis
Full Text:: , (Libocedrus Decurrens Torr.) Bark AN ABSTRACT OF THE THESIS OF James Edward Smith for the U.S. in

The chemical nature of the "lignin" of the bark of Douglas fir, Pseudotsuga menziesii (Mirb.) Franco

Creator:: Smith, James E. (James Edward)
Resource Type:: Dissertation
Full Text:: DOUGLAS FIR, · PSEUDOTSUGA MENZIESII (MffiB.) FRANCO by JAMES EDWARD ITH A THESIS submitted to

Polarization spectroscopy and photodissociation studies of nitroaromatic compounds in the gas phase

Creator:: Abbott, James E.
Abstract:: The central purpose of this dissertation was to explore and expand the use of an uniform electric field for orientation and for subsequent spectroscopic investigation of asymmetric polar molecules in the gas phase. The systems of study were nitrobenzene (NB) and the nitrotoluene (NT) isomers. We were able to quantitatively...
Resource Type:: Dissertation
Full Text:: DISSERTATION OF James E. Abbott, Jr. for the degree of Doctor of Philosophy in Chemistry presented on

Higher valence compounds of iron

Creator:: Schreyer, James Marlin
Resource Type:: Dissertation
Full Text:: OF IRON JAMES MARLIN SCIIREER A THESIS submitted to OREGON STATE COLLEGE in partial

The distribution and properties of the tannin in Douglas fir bark (Pseudotsuga taxifolia, Britt.)

Creator:: Hubbard, James Kenneth
Resource Type:: Masters Thesis
Full Text:: the condenser "D." The stopcock "E" is used to direct the flow of the percolate from "A.' Figure

Solubilization of acid nonextractable flavin-linked protein by cyanide

Creator:: Wu, James Tsai Yuan
Abstract:: It has been reported that cyanide inactivates the succinate dehydrogenase activity of HMP toward cytochrome c, oxygen, methylene blue and DCIP. In the present study, it was found that cyanide also solubilizes the SDH from HMP, this is reflected by the extent of solubilization of acid nonextractable flavin in the...
Resource Type:: Masters Thesis
Full Text:: AN ABSTRACT OF THE THESIS OF James Tsai Yuan Wu (Name of

Approaches to the total synthesis of verrucarol

Creator:: Hill, David E. (David Edwin) 1954-
Abstract:: Verrucarol is the sesquiterpene portion of a number of macrocyclic di- and triesters of potential medicinal importance. In this study, a novel approach to the synthesis of this fungal metabolite is presented. An A-B-C route was investigated in which C-3 and C-4 of the C-ring were emplaced using a [2+2]...
Resource Type:: Dissertation
Full Text:: ABSTRACT OF THE THESIS OF David E. Hill for the degree of Doctor of_Philosophy in Chemistry presented on

Studies towards the total synthesis of (-)-kendomycin

Creator:: Smits, Helmars
Abstract:: Studies towards the total synthesis of (−)-kendomycin (1), a bacterial metabolite with a unique molecular architecture and pronounced biological activity, are described. These studies resulted in the synthesis of advanced intermediate 208, containing all of the carbon atoms of 1. A Dötz annulation between alkyne 122 and novel chromium carbenoid...
Resource Type:: Dissertation
Full Text:: :_____________________________________________________ James D. White Studies towards the total synthesis of (−)-kendomycin (1), a bacterial

Part I: Synthesis and evaluation of synosutine as an inhibitor of serotonin, norepinephrine, and dopamine transporters Part II: Asymmetric approach to the tetracyclic core of neomangicol A

Creator:: Juniku, Rajan B.
Abstract:: Part I: Racemic and asymmetric syntheses of a new substance with prospective antidepressant properties were achieved. In vitro assays with synthetic racemates (±)-25 and (±)-26 suggested that the former is a relatively selective inhibitor of serotonin transporter whereas the latter is a more balanced inhibitor of both serotonin and norepinephrine...
Resource Type:: Dissertation
Full Text:: Abstract approved: _____________________________________________________ James D. White Part I

ScholarsArchive@OSU

Synthetic studies on marine natural products : I. Stereoselective synthesis of E,Z-1,3-Dienes by tandem nucleophilic addition to a dienylphosphonium salt followed by Wittig reaction. II. Synthesis of cyclopropyl oxylipins by a cation mediated carbocyclization

The nature of the chemical constituents of incense cedar, Libocedrus decurrens (Torr.) bark

The chemical nature of the "lignin" of the bark of Douglas fir, Pseudotsuga menziesii (Mirb.) Franco

Polarization spectroscopy and photodissociation studies of nitroaromatic compounds in the gas phase

Higher valence compounds of iron

The distribution and properties of the tannin in Douglas fir bark (Pseudotsuga taxifolia, Britt.)

Solubilization of acid nonextractable flavin-linked protein by cyanide

Approaches to the total synthesis of verrucarol

Studies towards the total synthesis of (-)-kendomycin

Part I: Synthesis and evaluation of synosutine as an inhibitor of serotonin, norepinephrine, and dopamine transporters Part II: Asymmetric approach to the tetracyclic core of neomangicol A

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