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STUDYING THE STEREOCHEMISTRY OF NAPROXEN USING ROTATIONALLY RESOLVED ELECTRONIC SPECTROSCOPY.

Please use this identifier to cite or link to this item: http://hdl.handle.net/1811/38125

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Title: STUDYING THE STEREOCHEMISTRY OF NAPROXEN USING ROTATIONALLY RESOLVED ELECTRONIC SPECTROSCOPY.
Creators: Young, Justin W.; Alvarez-Valtierra, Leonardo; Pratt, David W.
Issue Date: 2009
Abstract: Many biochemical processes are stereospecific. An example is the physiological response to a drug that depends on its enantiomeric form. Naproxen is a drug which shows this stereo-specific physiological response. To better understand the stereo specificity of chiral substances, we observed the S$_1\leftarrow$S$_0$ transitions of R- and S-naproxen in the gas phase using rotationally resolved electronic spectroscopy. The results will be discussed.
URI: http://hdl.handle.net/1811/38125
Other Identifiers: 2009-FA-11
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