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Studies Toward the Chemical Synthesis of Lacto-N-neotetraose

dc.creatorHayes, John Philip
dc.date.accessioned2020-08-22T17:42:46Z
dc.date.available2018-07-28
dc.date.issued2016-07-27
dc.identifier.urihttps://etd.library.vanderbilt.edu/etd-07202016-172138
dc.identifier.urihttp://hdl.handle.net/1803/13343
dc.description.abstractHuman milk oligosaccharides (HMOs) are a diverse class of carbohydrates that are unique to human milk. These oligosaccharides have been demonstrated to influence infant health through several mechanisms including helping to establish a healthy gut microbiome and deterring pathogenic infection. To understand the manner through which HMOs impart these benefits, it is important to conduct studies using single-entity compounds. The difficulty in isolating pure oligosaccharides from breastmilk has created a demand to access these carbohydrates synthetically. This work aimed to synthesize the human milk tetrasaccharide lacto-N-neotetraose. In the synthesis, an orthogonal protecting group strategy was employed to facilitate access to human milk pentasaccharides.
dc.format.mimetypeapplication/pdf
dc.subjecthuman milk oligosaccharide
dc.subjectHMO
dc.subjectcarbohydrate synthesis
dc.subjectcarbohydrates
dc.subjectlacto-n-neotetraose
dc.subjectLNnT
dc.subjecthuman milk tetrasaccharide
dc.subjectorthogonal protecting groups
dc.titleStudies Toward the Chemical Synthesis of Lacto-N-neotetraose
dc.typethesis
dc.contributor.committeeMemberGary Sulikowski
dc.type.materialtext
thesis.degree.nameMS
thesis.degree.levelthesis
thesis.degree.disciplineChemistry
thesis.degree.grantorVanderbilt University
local.embargo.terms2018-07-28
local.embargo.lift2018-07-28
dc.contributor.committeeChairSteven Townsend


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