Lake Superior State University
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Alum Success

Tyler graduated from Saline High School in Saline, Michigan. He has been an active leader at Anchorhouse Christian Fellowship. He completed his senior research on the use of microreactors to produce pharmaceutical precursors. He was the recipient of a GRO Fellowship for Undergraduates sponsored by the EPA. Tyler completed a summer working in Cinncinati for the EPA's National Risk Management Research Laboratory, and spent a summer in San Francisco with the American Chemical Society's Nuclear Summer School. Tyler will be pursuing his PhD at Washington State University in the Fall.

Tyler O'Dell
2010 Outstanding Graduate
Chemistry

Department of Environmental Sciences

Facilities & Equipment

Chemical Instrumentation

 


GIS Lab

16 GIS workstations with Arc GIS 10.1 & 36 inch poster plotter


Professional GPS Hardware

 

Field Sampling Equipment

Van Dorn bottles, flow meters, Hydrolab multiparamer sonde, Ponar dredge, drum samplers, battery powered sampling pumps, etc.


Hiltunen Field Station

~40 Acres with shoreline on Sugar Island in the St. Marys River

Towards the Synthesis of a Guanidine- like Organo- catalyst

Rebecca Smrke

In the last decade, N-based heterocycles have surfaced as useful organocatalysts. With strong Lewis basicity, a rigid structure that allows for strong resonance, and electronic distribution, these catalysts become useful in both medicinal and industrial chemistry purposes. The desire to created new and unique cyclic guanidine catalysts has generated interest in this field. We proposed to synthesize cyclic guanidine catalysts through a short three step process: (1) alkylation of a commercial imidazoline, (2) annulations with the use of a β-aminocarboxylic acid under dehydrating conditions, and (3) thermal elimination. The first step, alkylation, was successfully completed. In step 2, the annulations reaction, there is evidence that it may have proceeded, but more research is needed to verify the result. As such, the final step of forming an organocatalyst, elimination, could not be completed. In the future, the reaction will be optimized to yield the desired product.

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