Doctoral Dissertations
Part I. Enantioenrichment of α-hydroxy acids through lipase catalyzed esterification; Part II. Synthesis, purification and characterization of novel molecule, sulfonium (3-hydroxy-3-carboxypropyl)-dimethyl chloride; Part III. Synthesis, purification and characterization of potential cancer chemopreventive compound,2-hydroxy-4-(methyl seleno)-butanioc acid
Keywords and Phrases
Novel molecules
Abstract
"This dissertation is divided into three sections that cover three separate but related topics. The first section deals with a preparative scale separation of 2-Hydroxy-4-(methyl thio)-butanoic acid (HMTBA), the hydroxy analog of limiting amino acid Methionine (Met.)...The second section of the dissertation deals with the synthesis of S-methyl HMTBA, an analog of S-methyl methionine (SMM); Vitamin U...The research described in the third section was directed at the synthesis of a selenium analog of HMTBA (Se-HMTBA)--Abstract, page iii.
Advisor(s)
Kapila, Shubhender
Committee Member(s)
Ma, Yinfa
Ercal, Nuran
Nam, Paul Ki-souk
Forciniti, Daniel
Department(s)
Chemistry
Degree Name
Ph. D. in Chemistry
Sponsor(s)
Novus (Firm)
Publisher
University of Missouri--Rolla
Publication Date
Fall 2007
Pagination
xvi, 171 pages
Note about bibliography
Includes bibliographical references (pages 160-170).
Rights
© 2007 Shiva Garg, All rights reserved.
Document Type
Dissertation - Citation
File Type
text
Language
English
Subject Headings
Cancer -- ChemopreventionHydroxy acidsLipaseSelenium compoundsSulfur compounds
Thesis Number
T 9390
Print OCLC #
261216693
Recommended Citation
Garg, Shiva, "Part I. Enantioenrichment of α-hydroxy acids through lipase catalyzed esterification; Part II. Synthesis, purification and characterization of novel molecule, sulfonium (3-hydroxy-3-carboxypropyl)-dimethyl chloride; Part III. Synthesis, purification and characterization of potential cancer chemopreventive compound,2-hydroxy-4-(methyl seleno)-butanioc acid" (2007). Doctoral Dissertations. 1755.
https://scholarsmine.mst.edu/doctoral_dissertations/1755
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