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dc.contributor.advisorKiddle, James J.
dc.contributor.authorKim, Yejee C.
dc.date.accessioned2017-05-27T19:33:03Z
dc.date.available2017-05-27T19:33:03Z
dc.date.issued2016
dc.identifier.urihttp://hdl.handle.net/10920/30974
dc.descriptionv, 17 p.en_US
dc.description.abstractThe widespread use of antibiotics is polluting water systems that are giving rise to antibiotic resistant bacteria. Conventional water treatments are not effective in removing antibiotics from the water, which flow into ecosystems, allowing for bacteria to develop an immunity against the antibiotic. Resistant bacteria cause illnesses, such as salmonella, that are harder to treat with common antibiotics; thus, needing new antibiotics to combat the resistant bacteria. The antibiotics of interest are oxidized penicillin G derivatives that are not commercially available. By using coupling agents, 6-aminopenillic acid forms a peptide bond with aromatic phenols to produce the desired oxidized derivative. Protecting groups were also utilized to protect the carboxylic acids in the compounds. After attempting eight different reactions, an oxidized penicillin G derivative was not successfully synthesized. The reactivity of the carboxylic acids in 6-APA and the aromatic phenols posed a problem that was unable to be overcome.en_US
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen_US
dc.publisherKalamazoo Collegeen_US
dc.relation.ispartofKalamazoo College Chemistry Senior Individualized Projects Collection
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder. All rights reserved.
dc.titleSynthesis of Oxidized Penicillin G Derivativesen_US
dc.typeThesisen_US
KCollege.Access.ContactIf you are not a current Kalamazoo College student, faculty, or staff member, email dspace@kzoo.edu to request access to this thesis.


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  • Chemistry Senior Individualized Projects [860]
    This collection includes Senior Individualized Projects (SIP's) completed in the Chemistry Department. Abstracts are generally available to the public, but PDF files are available only to current Kalamazoo College students, faculty, and staff.

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