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Synthesis of phosphonopeptide transition state analogs of HIV-1 protease

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dc.contributor.author Lawrence, Kevin A.
dc.contributor.other Youngstown State University. Department of Chemistry.
dc.date.accessioned 2021-05-05T19:10:34Z
dc.date.available 2021-05-05T19:10:34Z
dc.date.issued 1995
dc.identifier.other B17307296
dc.identifier.uri https://jupiter.ysu.edu:443/record=b1730729
dc.identifier.uri http://hdl.handle.net/1989/16245
dc.description x, 47 leaves: figures, reference en_US
dc.description.abstract A focus of the research presented here is on the multi-step synthesis, isolation and characterization of phosphorous containing transition state analogs. Several procedures for the synthesis of the aminophosphonate core structure and side chain dipeptides were explored. These structures were designed to mimic the tetrahedral intermediate formed during the protease catalyzed hydrolysis of polypeptide substrates. As such, they are potential inhibitors of the HIV-1 protease enzyme. en_US
dc.description.sponsorship Youngstown State University. Department of Chemistry. en_US
dc.language.iso en_US en_US
dc.relation.ispartofseries Master's Theses;no. 0533
dc.title Synthesis of phosphonopeptide transition state analogs of HIV-1 protease en_US
dc.type Thesis en_US


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