Jason C. Rech, Ph.D.
Affiliations: | University of Pittsburgh, Pittsburgh, PA, United States |
Area:
Reaction Design, Total Synthesis, Mechanistic Analysis, Diversity Oriented SynthesisGoogle:
"Jason Rech"Mean distance: 8.43 | S | N | B | C | P |
Parents
Sign in to add mentorPaul 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 |