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Committee Member: Wulff, William D.
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Copyright Status: Creative Commons Licensed
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Electronic Theses & Dissertations
7
Material Type
Theses
7
Language
English
7
Subject
Alkaloids--Synthesis
1
Chemistry
1
Chemistry, Organic
4
Chirality
1
Design
1
Indole
1
Iridium catalysts
1
Organic reaction mechanisms
1
Organoboron compounds
1
Photoreceptors
1
Photovoltaic power generation
1
Protease inhibitors
1
Rapamycin
1
Stereochemistry
1
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Wittig rearrangements of silyl allylic cyclic ethers and [1,2] carbon to carbon silyl migration of alpha-hydroxy allyl silanes
Maloba, Emmanuel Wesonga
Text (2023)
Part of
Electronic Theses & Dissertations
Mechanistic studies of electrocatalytic processes : upgrading of lignin monomers to biofuels (probing substrate synergy); alkylation of amines with alcohols via borrowing hydrogen mechanisms; and reduction of the carboxylic acid functionality in amino ...
Appiagyei, Benjamin
Text (2020)
Part of
Electronic Theses & Dissertations
Catalytic asymmetric chlorofunctionalization reactions : mechanistic discoveries and advancements
Sarkar, Aritra
Text (2020)
Part of
Electronic Theses & Dissertations
CHEMOENZYMATIC SYNTHESIS OF HEPARAN SULFATE PROTEOGLYCAN AND MIMETICS
Gao, Jia
Text (2021)
Part of
Electronic Theses & Dissertations
I. A covalent/computational approach for sensing chirality. II. Oxidative functionalization of the indole core. III. Design and synthesis of novel cyanine dyes as photoreceptors for photovoltaics
Zhang, Jun (Scientist)
Text (2018)
Part of
Electronic Theses & Dissertations
The design and synthesis of novel proteasome inhibitors : studies on the synthesis of nagelamide M and analogs, the synthesis of rapamycin based proteasome inhibitors, and the synthesis of TCH based molecular probes for binding site determination
Giletto, Matthew Basil
Text (2017)
Part of
Electronic Theses & Dissertations
Advancing frontiers in reactive and selective iridium c-h borylation catalysis and targeted silsesquioxane synthesis
Dannatt, Jonathan E.
Text (2019)
Part of
Electronic Theses & Dissertations
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