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Huw Davies

Asa Griggs Candler Professor

Chemistry Building
Department of Chemistry
Emory University
Atwood Hall 440
Atlanta, GA 30322

404-727-6839

Email: hmdavie@emory.edu

Davies Group Home Page


The department of chemistry is delighted to announce that Professor Huw M. L. Davies will be joining our faculty in August of 2008.

Huw M. L. Davies was born in Aberystwyth, Wales. He received his B. Sc. degree from University College Cardiff, Wales in 1977 and his Ph. D degree from the University of East Anglia, England in 1980.

After a post-doctoral position at Princeton University, he joined the faculty at Wake Forest University. In 1995 he moved to the State University of New York at Buffalo and will be joining the Chemistry department at Emory in the summer of 2008. His research interests include: catalytic asymmetric C-H activation, new synthetic methodology based on carbenoid intermediates, chiral catalysts for asymmetric synthesis, total synthesis of biologically active natural products, and development of chiral therapeutic agent. Dr Davies has published over 170 articles and holds 10 patents. He is the recipient of a 2005 Cope Scholar Award and was recently the Chair of the Organic Division of the American Chemical Society.

A recent review article published in Nature describes some of the effort curently underway in the Davies laboratory. A new chemical synthesis method based on a catalyst worth many times the price of gold and providing a far more efficient and economical method than traditional ones for designing and manufacturing extremely novel pharmaceutical compounds is a major focus of his research. This chemistry has the potential to improve dramatically the design and production of new drugs based on small molecule organic compounds, which comprise the great majority of new drug applications.

As rhodium metal costs 10 times the price of gold, the catalyst is a high-value material. Available through chemical supply companies, the reagents are being used by pharmaceutical scientists in both industry and academia. A major advantage of Davies' chemical strategy is that the resulting compounds are produced selectively as single mirror images. Pharmaceutical companies prefer to develop new chiral drugs (chiral meaning "handed") as a single isomer because opposite mirror images can have different biological effects and may be harmful. A small amount of the rhodium(II) catalyst can be used to generate large amounts of the active mirror image of the pharmaceutical ingredient.

The research being carried out by the Davies group has been funded by the National Institutes of Health and the National Science Foundation, both of which were recently renewed for a total of $1.6 million.

 

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Last updated: October 13, 2009
Please direct questions or comments to sal2@emory.edu