Jason C. Rech, Ph.D.

Affiliations: 
University of Pittsburgh, Pittsburgh, PA, United States 
Area:
Reaction Design, Total Synthesis, Mechanistic Analysis, Diversity Oriented Synthesis
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Parents

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Paul E. Floreancig grad student 2005 University of Pittsburgh
 (The development of an electron transfer initiated cyclization approach toward the total synthesis of mycalamide B. The synthesis of the N(7)-C(25) fragment of psymberin.)
Jonathan A. Ellman post-doc 2007 UC Berkeley College of Chemistry
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Publications

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Wan S, Wu F, Rech JC, et al. (2011) Total synthesis and biological evaluation of pederin, psymberin, and highly potent analogs. Journal of the American Chemical Society. 133: 16668-79
Floreancig P, Green M, Rech J. (2009) Synthesis of Theopederin D Synfacts. 2009: 0234-0234
Green ME, Rech JC, Floreancig PE. (2008) Total synthesis of theopederin D Angewandte Chemie - International Edition. 47: 7317-7320
Nakagawa H, Rech JC, Sindelar RW, et al. (2007) Catalytic enantioselective addition of arylboronic acids to N-boc imines generated in situ. Organic Letters. 9: 5155-7
Rech JC, Yato M, Duckett D, et al. (2007) Synthesis of potent bicyclic bisarylimidazole c-Jun N-terminal kinase inhibitors by catalytic C-H bond activation. Journal of the American Chemical Society. 129: 490-1
Rech JC, Floreancig PE. (2005) Concise and stereoselective synthesis of the N7-C25 fragment of psymberin Organic Letters. 7: 5175-5178
Green ME, Rech JC, Floreancig PE. (2005) Stereochemical assignment of the C1-C6 fragment of psymberin by synthesis and natural product degradation Organic Letters. 7: 4117-4120
Aubele DL, Rech JC, Floreancig PE. (2004) Catalytic Aerobic Generation of Acyliminium Ions through Electron‐Transfer‐Mediated Carbon‐Carbon Bond Activation Advanced Synthesis & Catalysis. 346: 359-366
Aubele DL, Rech JC, Floreancig PE. (2004) Catalytic aerobic generation of acyliminium ions through electron-transfer-mediated carbon-carbon bond activation Advanced Synthesis and Catalysis. 346: 359-366
Rech JC, Floreancig PE. (2003) An oxidative entry into the amido trioxadecalin ring system Organic Letters. 5: 1495-1498
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