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dc.contributor.advisorNesnas, Nasri
dc.contributor.authorNascimento, Carolina
dc.contributor.authorFaylough, Samira
dc.contributor.authorGuruge, Charitha
dc.contributor.authorStruts, Andrey
dc.contributor.authorBrown, Michael F.
dc.contributor.authorNesnas, Nasri
dc.date2015-04
dc.date.accessioned2015-09-01T18:59:50Z
dc.date.available2015-09-01T18:59:50Z
dc.identifier.citationNascimento, C., Faylough, S., Guruge, C., Struts, A., Brown, M., Nesnas, N. (2015, April). Synthesis of Deuterated-(C9)-11-cis-Retinal. Poster presented at the Northrop Grumman Engineering & Science Student Design Showcase, Florida Institute of Technology, Melbourne, FL.en_US
dc.identifier.urihttp://hdl.handle.net/11141/714
dc.description.abstractIt has been shown that the dimerization of 2 vitamin A molecules with an Ethanolamine molecule leads to the formation of a molecule labeled as A2E. The latter is a phototoxic molecule and has been shown to be a major contributor to the detrimental eye condition, Age-related Macular Degeneration, AMD (1). Even though vitamin A dimerization is a contributor to this AMD condition, vitamin A is the very molecule that is necessary and key for human vision, hence it cannot be eliminated. It is been demonstrated experimentally that once carbon 20 of vitamin A was deuterated, the dimerization of vitamin A was reduced (1). Synthesis of retinal, one of many forms of vitamin A, has been well established (2, 3) and can be used to study vitamin A structure. Using similar synthetic routes and methods, we were able to introduce deuterium on carbon 9 of 11-cis-retinal.en_US
dc.language.isoen_USen_US
dc.titleSynthesis of Deuterated-(C9)-11-cis-Retinalen_US
dc.typeposteren_US


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