When: Wednesday, January 29, 2014 [9:30 AM - 12:00 PM]
Where: Bldg. 9 Classroom # 3125
Where: Bldg. 9 Classroom # 3125
Description
The environmentally friendly industrial synthesis/production of many life-saving medicines is a very important task for pharmaceutical companies. Less waste and fewer steps to obtain the target molecules means cheaper medicines for patients. Given that today more than half of the approved medicines have one or more chiral centers and they are sold as single enantiomers, catalytic asymmetric methods are increasingly employed in the production of the active pharmaceutical ingredients (APIs). In the past when racemic synthesis was used in the production phase, 50% of the material had to be discarded as it was the opposite enantiomer that could not be utilized as a drug. The course will examine several key green chemistry principles as well as several strategies for asymmetric synthesis. Case studies will be presented on the synthesis of Sitagliptin (Januvia), Efavirenz (Sustiva) and Tolterodin. Anticipated audience: Students who have taken general chemistry and introductory organic chemistry.Laszlo Kurti
While still in graduate school, he authored the now popular book "Strategic Applications of Named Reactions in Organic Synthesis" with Dr. Barbara Czakó that is now used in dozens of academic institutions worldwide. In 2007 he co-authored the book "Molecules and Medicine" with Prof. E.J. Corey and Dr. Barbara Czakó. In September 2010, László joined the faculty at UT Southwestern Medical Center, Dallas Texas, as an Assistant Professor in the Department of Biochemistry.
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