Since the discovery that organic molecules could be synthesized in a lab, the teaching and practice of synthetic organic chemistry has revolved around the classification and reaction of compounds according to the functional groups they contain. A basic precept of all introductory organic chemistry texts is the contrast between the reactivity of functional groups and the âinertâ C-H and C-C bonds that make up the skeleton of just about every organic molecule. C-H Functionalization offers an alternative to this mode of thinking, through the development and application of effective and robust catalysts capable of transformations that selectively convert a C-H bond into the functional group or structural motif of choice.
This strategy for constructing molecules has the potential to broadly impact not only synthetic organic chemistry, but also the disciplines that rely on this highly enabling field, such as the pharmaceutical, material and agrochemical sciences. The C-H functionalization approach embodies many of the drivers that motivate modern science and can be summarized as a truly sustainable strategy by four key statements; 1). As a primarily catalytic transformation only very small amounts of high value reagents (catalysts) are required to convert large amounts of feedstock chemicals into essential commodities. 2). Employing a C-H bond as the reaction partner removes the need for introduction or inter-conversion of functional groups, significantly expanding the scope of feedstock chemicals available for reaction and thus 3). considerably reducing the number of operations required to achieve a desired molecular change. 4). A meaningful reduction in the volume of hazardous waste generated by using the C-H bond as a reaction partner (typical byproducts include hydrogen and nitrogen gas or water).
This field is at a stage where expertise from across the chemical sciences is required to truly establish a main stream technology. The aim of this workshop is to bring together the leading and emerging practitioners of C-H functionalization to discuss the many exciting potential applications of this technology and how to accelerate adoption of this science. At this stage, one of the critical elements is to understand the mechanistic aspects of these reactions in order to develop a rational approach for how to achieve site- and enantioselective transformations. Computational and experimental physical organic chemists are playing a pivotal role in this field, informing and guiding catalyst and reaction design. A forum that brings together these perspectives will provide an enriching experience for the participants and hopefully the field more broadly.
The registration fee includes breakfast on each workshop day.
We wish to ensure an intimate workshop setting, with no more than 20 to 25 participants. If you are interested in attending, but have not received an invitation, please contact the workshop organizer before registering. If you have registered for a meeting you were not invited to, you may be subject to a $100 fee.
TSRC is about expanding the frontiers of science, exploring new ideas, and building collaborations. The workshop schedule will allow for substantial unstructured time for participants to talk and think. All participants are expected to stay for the entire duration of the workshop. Scientists are encouraged to consider bringing family or friends. Telluride offers a number of options for children's camps (including Telluride Academy, Aha School for the Arts, and Pinhead Institute). There is more information on childcare, camps, and family activities on TSRC's website. Feel free to contact TSRC's staff to help with any planning and/or coordinating care.
Telluride Intermediate School
725 W Colorado Ave., Telluride CO 81435
|Ackermann, Lutz||Georg-August-University GÃ¶ttingen, Institute for Organic and Biomolecular Chemistry|
|Alexanian, Erik||University of North Carolina at Chapel Hill|
|Blackmond, Donna G.||Scripps Research|
|Davies, Huw||Emory University|
|Ellman, Jonathan||Yale University|
|Hilinski, Michael||University of Virginia|
|Hoover, Jessica||West Virginia University|
|Huang, Xiongyi||California Institute of Technology|
|Krska, Shane W.||Merck & Co., Inc.|
|Lewis, Jared C.||Indiana University|
|Lindsay, Vincent||North Carolina State University|
|Montgomery, John||University of Michigan|
|Musaev, Jamal||Emory University|
|Nagib, David||The Ohio State University|
|Narayan, Alison||University of Michigan|
|Narayan, Alison [2nd Reservation]||University of Michigan|
|Nelson, Hosea M.||UCLA|
|Neufeldt, Sharon||Montana State University|
|Renata, Hans||The Scripps Research Institute|
|Roizen, Jennifer||Duke University|
|Roizen, Jennifer [2nd Reservation]||Duke University|
|Romo, Rubén Martín||ICIQ|
|Seidel, Daniel||University of Florida|
|Tambar, Uttam||UT Southwestern Medical Center|
|Voight, Eric [2nd Reservation]||AbbVie|
|Wasa, Masayuki||Boston College|