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[2015-10-26]Hao Xu:Iron-Catalyzed Stereoselective Olefin Aminohydroxylation and Aminofluorination Reactions
发表日期: 2015-10-26 作者: 文章来源:
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报告人:Professor Hao Xu (顼昊)

Georgia State University, Department of Chemistry

时  间:2015年10月28日(星期三)

上午10:00

地  点:成都生物所高新园区5楼会议室

 

 顼昊教授简历:

 Hao Xu went to Peking University (Beijing) for college in 1997.  He enrolled in the Chemistry Graduate Program at Scripps Research Institute (La Jolla, CA) in 2001 and carried out his Ph.D. research with Professor K.C. Nicolaou for complex-molecule synthesis.  In 2006, he joined Professor Eric Jacobsen’s lab at Harvard University (Cambridge, MA) as a Dreyfus Postdoctoral Fellow.He joined the faculty of Georgia State University (Atlanta, GA) in Fall 2010.

 Hao has been recognized by a list of accolades, including Skaggs Predoctoral Fellowship (2003), Shelton Award in Graduate Studies (2005), Bristol-Myers Squibb Graduate Fellowship in Synthetic Organic Chemistry (2006), Camille and Henry Dreyfus Postdoctoral Fellowship (2007), Thieme Chemistry Journal Award (2014), National Science Foundation (NSF) CAREER Award (2014), Dean’s Early Career Award at Georgia State (2015), CAPA Biomatick Distinguished Junior Faculty Award (2015), and most recently Alfred P. Sloan Research Fellowship (2015).

 报告摘要:

 Numerous pharmaceuticals contain at least one nitrogen atom and many of those nitrogen atoms are directly attached to stereogenic centers. Therefore, synthetic methods that incorporate selective nitrogen atom transfer to readily available hydrocarbons are important tools for the synthesis of these valuable molecules. While methods for selective olefin aziridination and direct C-H amination are well-established, methods for direct difunctionalization of olefins with a nitrogen atom and a range of heteroatom-based functional groups are less explored yet critically important to organic synthesis and its applications to the biomedical sciences.  The lecture is about the discovery and development of a series of iron-catalyzed nitrogen atom transfer reactions with an emphasis on stereoselective olefin aminohydroxylation and aminofluorination reactions.


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