Mohr, Justin - The University of Illinois at Chicago

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“Regiodivergent Halogenation of Vinylogous Esters: One-Pot, Transition Metal-Free Access to Differentiated Haloresorcinols" Chen, X.; Martinez, J. S.; Mohr, J. T. Org. Lett. 2015, 17, 378–381 “Formal total syntheses of classic natural product target molecules via palladium-catalyzed enantioselective alkylation" Liu, Y.; Liniger, M.; McFadden, R. M.; Roizen, J. L.; Malette, J.; Reeves, C. M.; Behenna, D. C.; Seto, M.; Kim, J.; Mohr, J. T.; Virgil, S. C.; Stoltz, B. M. Beilstein J. Org. Chem. 2014, 10, 2501–2512. [Supporting Information] “The Reaction Mechanism of the Enantioselective Tsuji Allylation: Inner-Sphere and Outer-Sphere Pathways, Internal Rearrangements and Asymmetric C-C Bond Formation” Keith, J. A.; Behenna, D. C.; Sherden, N.; Mohr, J. T.; Ma, S.; Marinescu, S. C.; Nielsen, R. J.; Oxgaard, J.; Stoltz, B. M.; Goddard III, W. A. J. Am. Chem. Soc. 2012, 134, 19050–19060. [Supporting Information] “Competitive Activity-Based Protein Profiling Identifies Aza-β-Lactams as a Versatile Chemotype for Serine Hydrolase Inhibition” Zuhl, A. M.; Mohr, J. T.; Bachovchin, D. A.; Niessen, S.; Hsu, K.-L.; Berlin, J. M.; Dochnahl, M.; López-Alberca, M. P.; Fu,G. C.; Cravatt, B. F. J. Am. Chem. Soc. 2012, 134, 5068–5071. [Supporting Information] “Enantioselective Decarboxylative Alkylation Reactions: Catalyst Development, Substrate Scope, and Mechanistic Studies” Behenna, D. C.; Mohr, J. T.; Sherden, N. H.; Marinescu, S. C.; Harned, A. M.; Tani, K.; Seto, M.; Ma, S.; Novák, Z.; Krout, M. R.; McFadden, R M; Roizen, J. L.; Enquist Jr., J. A.; White, D. E.; Levine, S. R.; Petrova, K. V.; Iwashita, A.; Virgil, S. C.; Stoltz, B. M. Chem.–Eur. J. 2011, 17, 14199–14223. [Supporting Information] “Protonation, Alkylation, Arylation, and Vinylation of Enolates” Stoltz, B. M.; Mohr, J. T. In Stereoselective Synthesis, Vol. 3 (P. A. Evans, Ed.) Chapter 3.15 (2011), pp. 615–674. “Academic Cross-fertilization by Public Screening Yields a Remarkable Class of Protein Phosphatase Methylesterase-1 Inhibitors” Bachovchin, D. A.; Mohr, J. T.; Speers, A. E.; Wang, C.; Berlin, J. M.; Spicer, T. P.; Fernandez-Vega, V.; Chase, P.; Hodder, P. S.; Schürer, S. C.; Nomura, D. K.; Rosen, H.; Fu, G. C.; Cravatt, B. F. Proc. Natl. Acad. Sci. U.S.A. 2011, 108, 6811–6816. [Supporting Information] “Enantioselective Protonation” Mohr, J. T.; Hong, A. Y.; Stoltz, B. M. Nature Chem. 2009, 1, 359–369. “Preparation of (S)-2-Allyl-2-methylcyclohexanone” Mohr, J. T.; Krout, M. R.; Stoltz, B. M. Org. Synth. 2009, 86, 194–211. “Preparation of (S)-tert-ButylPHOX” Krout, M. R.; Mohr, J. T.; Stoltz, B. M. Org. Synth. 2009, 86, 181–193. “Enantioselective Total Synthesis of (+)-Cassiol” Petrova, K. V.; Mohr, J. T.; Stoltz, B. M. Org. Lett. 2009, 11, 293–295. [Supporting Information] “Natural Products as Inspiration for Development of Asymmetric Catalysts” Mohr, J. T.; Krout, M. R.; Stoltz, B. M. Nature 2008, 455, 323–332. “Homogeneous Pd-Catalyzed Enantioselective Decarboxylative Protonation” Marinescu, S. C.; Nishimata, T.; Mohr, J. T.; Stoltz, B. M. Org. Lett. 2008, 10, 1039–1042. [Supporting Information] “Enantioselective Tsuji Allylations” Mohr, J. T.; Stoltz, B. M. Chem.–Asian J. 2007, 2, 1476–1491. “Catalytic Enantioselective Stereoablative Reactions: An Unexploited Approach to Enantioselective Catalysis” Mohr, J. T.; Ebner, D. C.; Stoltz, B. M. Org. Biomol. Chem. 2007, 5, 3571–3576. “The Inner-Sphere Process in the Enantioselective Tsuji Allylation Reaction with (S)-t-Bu-phosphinooxazoline (PHOX) Ligands” Mohr, J. T.; Nishimata, T.; Behenna, D. C.; Stoltz, B. M. J. Am. Chem. Soc. 2006, 128, 11348–11349. [Supporting Information] “Process for Enantioselective Allylation of Ketones and Olefins” Behenna, D. C.; Stoltz, B. M.; Mohr, J. T.; Harned, A. M. United States Patent, US 7235698, 2007. “Catalytic Enantioselective Decarboxylative Protonation” Mohr, J. T.; Nishimata, T.; Behenna, D. C.; Stoltz, B. M. J. Am. Chem. Soc. 2006, 128, 11348–11349. [Supporting Information] "Deracemization of Quaternary Carbon Stereocenters by Pd-Catalyzed Enantioconvergent Decarboxylative Allylation of Racemic β-Ketoesters" Mohr, J. T.; Behenna, D. C.; Harned, A. M.; Stoltz, B. M. Angew. Chem., Int. Ed. 2005, 44, 6924–6927. [Supporting Information] "Anesthetic Potency of Two Novel Synthetic Polyhydric Alkanols Longer than the n-Alkanol Cutoff: Evidence for a Bilayer-Mediated Mechanism of Anesthesia?" Mohr, J. T.; Gribble, G. W.; Lin, S. S.; Eckenhoff, R. G.; Cantor, R. S. J. Med. Chem. 2005, 48, 4172–4176.

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