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dc.contributor.advisorKelly, Jeffrey W.
dc.creatorZacharias, Niki
dc.date.accessioned2022-04-01T15:06:56Z
dc.date.available2022-04-01T15:06:56Z
dc.date.issued1997
dc.identifier.urihttps://hdl.handle.net/1969.1/CAPSTONE-ZachariasN_1997
dc.descriptionProgram year: 1996/1997en
dc.descriptionDigitized from print original stored in HDRen
dc.description.abstractDr. Jeff Kelly's laboratory has been using 4-(2-aminoethyl)-6-dibenzofuran propoinic acid an unnatural amino acid to initiate 𝛽 sheet folding. The unnatural amino acid mimics a 𝛽 tum in an antiparallel 𝛽 sheet structure. Peptides that incorporate the dibenzofuran based unnatural amino acid are being used to study the mechanism of folding and the synthesis of novel materials. A new synthesis of 4-(2-aminoethyl)-6-dibenzofuran propoinic acid has been created. The synthesis has a high yield and simple purification. The synthesis is based on the desymmetrization of the dibenzofuran ring using a monosilylation reaction.en
dc.format.extent29 pagesen
dc.format.mediumelectronicen
dc.format.mimetypeapplication/pdf
dc.subject𝛽 sheet foldingen
dc.subjectunnatural amino aciden
dc.subjectfoldingen
dc.subjectnovel materialsen
dc.subjectsynthesisen
dc.titleSynthesis of 4-(2-aminoethyl)-6-dibenzofuran propoinic acid: An Unnatural Amino Acid that initializes B sheet Foldingen
dc.title.alternativeSynthesis of 4-(2-aminoethyl)-6-dibenzofuran propoinic acid: An Unnatural Amino Acid that initializes B sheet Foldingen
dc.typeThesisen
thesis.degree.departmentChemistryen
thesis.degree.grantorUniversity Undergraduate Fellowen
thesis.degree.levelUndergraduateen
dc.type.materialtexten


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