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University of Illinois at Urbana-Champaign

Part I. A Novel Vitamin B(12) Catalyzed Carbon-Carbon Bond Forming Reaction: Mechanistic Investigations and Aryl Alkene Cyclization. Part II. Mechanistic Investigation of Prostaglandin H Synthase Through the Synthesis of Site Specifically Substituted Arachidonic Acids

Abstract

dc:description

Finally, the syntheses of site-specifically deuterated arachidonic acids containing a remote tritium label are reported. These radiolabeled substrates would allow the characterization of the initial radical intermediate for PGHS under aerobic conditions and enzyme turnover. The substrates could also be used to investigate other oxygenase enzymes, such as lipoxygenases and aspirin-treated PGHS.

Degree

thesis:*
Name thesis:degree_name
Ph.D.
Level thesis:degree_level
Dissertation
Discipline thesis:degree_discipline
Chemistry
Grantor
University of Illinois at Urbana-Champaign
Year dc:date
2015

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • McGinley, Christopher
Contributors dc:contributor
  • van der Donk, Wilfred A.

Subjects

dc:subject × 1

Rights

Language dc:language
eng

Identifiers

dc:identifier.*
Identifier
(MiAaPQ)AAI3199081
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/84194

Chain of custody

source
Harvested from
University of Illinois - Urbana-Champaign
Base URL
www.ideals.illinois.edu/oai-pmh
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

McGinley, Christopher. Part I. A Novel Vitamin B(12) Catalyzed Carbon-Carbon Bond Forming Reaction: Mechanistic Investigations and Aryl Alkene Cyclization. Part II. Mechanistic Investigation of Prostaglandin H Synthase Through the Synthesis of Site Specifically Substituted Arachidonic Acids. Dissertation thesis, University of Illinois at Urbana-Champaign, 2015. http://hdl.handle.net/2142/84194