Event Title
The Development of Synthetic Pathways Towards Melanin Analogs
Location
Science Center, Bent Corridor
Start Date
10-2-2015 12:00 PM
End Date
10-2-2015 1:20 PM
Poster Number
28
Abstract
Melanins are some of the least understood biopolymers, but they have the potential to have a significant positive impact, potentially acting as water purification tools and organic semiconductors. Of the three different kinds of melanin, the type being studied in the Belitsky lab is eumelanin, the form that gives rise to black and brown coloration in hair and skin. Currently, the Belitsky lab is carrying out a series of reactions on functionalized indoles, compounds that when trimerized likely emulate the characteristics of eumelanin. Unlike eumelanin, these compounds are relatively easy to work with, meaning that they function as useful analogs of the biopolymer. This reaction series will hopefully help us better understand efficient synthetic pathways for this trimerization. Specifically, we are currently working on modifications of the Suzuki-Miyaura coupling reaction, such that we achieve coupling at the desired sites on the indoles.
Recommended Citation
Quirke, Jonathan; Levy, Jeff; and Ryu, Harry, "The Development of Synthetic Pathways Towards Melanin Analogs" (2015). Celebration of Undergraduate Research. 31.
https://digitalcommons.oberlin.edu/cour/2015/posters/31
Major
Chemistry and Biochemistry
Project Mentor(s)
Jason Belitsky, Chemistry
Document Type
Poster
The Development of Synthetic Pathways Towards Melanin Analogs
Science Center, Bent Corridor
Melanins are some of the least understood biopolymers, but they have the potential to have a significant positive impact, potentially acting as water purification tools and organic semiconductors. Of the three different kinds of melanin, the type being studied in the Belitsky lab is eumelanin, the form that gives rise to black and brown coloration in hair and skin. Currently, the Belitsky lab is carrying out a series of reactions on functionalized indoles, compounds that when trimerized likely emulate the characteristics of eumelanin. Unlike eumelanin, these compounds are relatively easy to work with, meaning that they function as useful analogs of the biopolymer. This reaction series will hopefully help us better understand efficient synthetic pathways for this trimerization. Specifically, we are currently working on modifications of the Suzuki-Miyaura coupling reaction, such that we achieve coupling at the desired sites on the indoles.