Approaches toward the Chemical Synthesis of Novel Arachidonic Acid Metabolites Hemiketal D2 and Hemiketal E2

Hemiketal D2 and hemiketal E2 are eicosanoids identified by Schneider and coworkers in 2011. These novel arachidonic acid metabolites are cross-over products of the enzymes 5-LOX and COX-2, previously assumed to be operating independently in the biosynthesis of leukotrienes and prostaglandins, respe...

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Main Author: Boer, Robert Edward
Other Authors: Professor Gary A. Sulikowski
Format: Others
Language:en
Published: VANDERBILT 2015
Subjects:
Online Access:http://etd.library.vanderbilt.edu/available/etd-06042015-085510/
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spelling ndltd-VANDERBILT-oai-VANDERBILTETD-etd-06042015-0855102015-06-06T05:21:08Z Approaches toward the Chemical Synthesis of Novel Arachidonic Acid Metabolites Hemiketal D2 and Hemiketal E2 Boer, Robert Edward Chemistry Hemiketal D2 and hemiketal E2 are eicosanoids identified by Schneider and coworkers in 2011. These novel arachidonic acid metabolites are cross-over products of the enzymes 5-LOX and COX-2, previously assumed to be operating independently in the biosynthesis of leukotrienes and prostaglandins, respectively. It was shown that the hemiketals stimulate angiogenesis of vascular endothelial cells, suggesting these compounds may be involved in inflammation and tissue repair. As the enzymatic production of these compounds is low yielding, chemical synthesis provides an attractive option for their production for further study. Thus, chapter 1 discusses the biological importance of lipid mediators and inflammation and previous synthetic approaches to these compounds. Chapter 2 details the proposed cycloisomerization/oxidation strategy to access the structurally intriguing keto-hemiketal moiety and the initial approaches toward the synthesis of hemiketal E2. Chapter 3 highlights the completion of the synthesis of hemiketal E2 and the progress toward a deuterated version of hemiketal E2. Chapter 4 discusses the progress made toward the synthesis of the related hemiketal D2. Professor Gary A. Sulikowski Professor Jeffrey N. Johnston Professor Claus Schneider Professor Brian O. Bachmann VANDERBILT 2015-06-05 text application/pdf http://etd.library.vanderbilt.edu/available/etd-06042015-085510/ http://etd.library.vanderbilt.edu/available/etd-06042015-085510/ en restricted I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to Vanderbilt University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report.
collection NDLTD
language en
format Others
sources NDLTD
topic Chemistry
spellingShingle Chemistry
Boer, Robert Edward
Approaches toward the Chemical Synthesis of Novel Arachidonic Acid Metabolites Hemiketal D2 and Hemiketal E2
description Hemiketal D2 and hemiketal E2 are eicosanoids identified by Schneider and coworkers in 2011. These novel arachidonic acid metabolites are cross-over products of the enzymes 5-LOX and COX-2, previously assumed to be operating independently in the biosynthesis of leukotrienes and prostaglandins, respectively. It was shown that the hemiketals stimulate angiogenesis of vascular endothelial cells, suggesting these compounds may be involved in inflammation and tissue repair. As the enzymatic production of these compounds is low yielding, chemical synthesis provides an attractive option for their production for further study. Thus, chapter 1 discusses the biological importance of lipid mediators and inflammation and previous synthetic approaches to these compounds. Chapter 2 details the proposed cycloisomerization/oxidation strategy to access the structurally intriguing keto-hemiketal moiety and the initial approaches toward the synthesis of hemiketal E2. Chapter 3 highlights the completion of the synthesis of hemiketal E2 and the progress toward a deuterated version of hemiketal E2. Chapter 4 discusses the progress made toward the synthesis of the related hemiketal D2.
author2 Professor Gary A. Sulikowski
author_facet Professor Gary A. Sulikowski
Boer, Robert Edward
author Boer, Robert Edward
author_sort Boer, Robert Edward
title Approaches toward the Chemical Synthesis of Novel Arachidonic Acid Metabolites Hemiketal D2 and Hemiketal E2
title_short Approaches toward the Chemical Synthesis of Novel Arachidonic Acid Metabolites Hemiketal D2 and Hemiketal E2
title_full Approaches toward the Chemical Synthesis of Novel Arachidonic Acid Metabolites Hemiketal D2 and Hemiketal E2
title_fullStr Approaches toward the Chemical Synthesis of Novel Arachidonic Acid Metabolites Hemiketal D2 and Hemiketal E2
title_full_unstemmed Approaches toward the Chemical Synthesis of Novel Arachidonic Acid Metabolites Hemiketal D2 and Hemiketal E2
title_sort approaches toward the chemical synthesis of novel arachidonic acid metabolites hemiketal d2 and hemiketal e2
publisher VANDERBILT
publishDate 2015
url http://etd.library.vanderbilt.edu/available/etd-06042015-085510/
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