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
McGinley, Christopher
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Permalink
https://hdl.handle.net/2142/84194
Description
Title
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
Author(s)
McGinley, Christopher
Issue Date
2005
Doctoral Committee Chair(s)
van der Donk, Wilfred A.
Department of Study
Chemistry
Discipline
Chemistry
Degree Granting Institution
University of Illinois at Urbana-Champaign
Degree Name
Ph.D.
Degree Level
Dissertation
Keyword(s)
Chemistry, Biochemistry
Language
eng
Abstract
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.
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