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Full-Text Articles in Physical Sciences and Mathematics
Development Of 1,2-Cis-Selective Glycosylation Protocols And Multistep Synthesis Of Glycans From Acinetobacter Baumannii., Dancan Kamau Njeri
Development Of 1,2-Cis-Selective Glycosylation Protocols And Multistep Synthesis Of Glycans From Acinetobacter Baumannii., Dancan Kamau Njeri
LSU Doctoral Dissertations
Access to various oligosaccharides has been made possible by glycosylation reactions. This is mainly through chemical synthesis and enzymatic approaches. Herein, I talk about glycosylation through chemical synthesis. In general, glycosylation reactions lead to a mixture of 1,2-cis and 1,2-trans stereoisomers. Stereoselective access to 1,2-trans isomer is highly developed; it efficiently relies on neighboring group participation. However, efficient access to 1,2-cis selective glycosylation is still a work in progress. In Chapter 1, I highlight notable efforts developed so far that address the 1,2-cis selectivity challenge in glycosylation.
In Chapter 2, I demonstrate how I improved …
New Synthetic Reactions Enabled By Protected Oxyallyl And Amidoallyl Cations, Binod Nepal
New Synthetic Reactions Enabled By Protected Oxyallyl And Amidoallyl Cations, Binod Nepal
LSU Doctoral Dissertations
This dissertation entails design and development of two new synthetic methodologies made possible through the generation of cationic species, namely oxyallyl and amidoallyl cations. Chapter 1 involves literature survey on generation and trapping of oxyallyl cations. Mostly known for cycloaddition reactions with these elusive species, the most recent approach of direct nucleophilic capture of oxyallyl cations are discussed. Apt design of substrates and reaction conditions by Kartika Group to access a-electrophilic carbon towards the synthesis of a variety of value-added compounds, i.e., 1,4- and 1,6-dicarbonyls, carbazoles, densely substituted pyrroles and furans are elaborated.
Chapter 2 focuses on our discovery of …