Studying the Stereochemistry of Naproxen Using Rotationally Resolved Electronic Spectroscopy.

Details Studying the Stereochemistry of Naproxen Using Rotationally Resolved Electronic Spectroscopy. Studying the Stereochemistry of Naproxen Using Rotationally Resolved Electronic Spectroscopy.

Jun 2009

adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=2009mss..confefa11y&link_type=abstract

"International Symposium On Molecular Spectroscopy, 64th Meeting, Held 22-26 June, 2009 at Ohio State University. http://molspec

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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←S_0 transitions of R- and S-naproxen in the gas phase using rotationally resolved electronic spectroscopy. The results will be discussed.

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