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Publications

  • De Oliveira Silva, A.; Masand, S.; Farah, A. O.; Laddusaw, J.; Urbina, K.; Rodríguez-Alvarado, M.; Lalancette, R.; Cheong, P. H.-Y.*; Brenner-Moyer, S. E.* “Organocatalytic enantioselective [1,2]-Stevens rearrangement of azetidinium salts.” J. Org. Chem. 2024, 89, 9063-9067. (Abstract)

    **Highlighted in Synfacts

  • De Oliveira Silva, A.; Harper, J. L.; Fuhr, K. N.; Lalancette, R. A.; Cheong, P. H.-Y.*; Brenner-Moyer, S. E.* “DyKAT by DiCat: Stereoconvergent dienamine-catalyzed Claisen rearrangements.” J. Org. Chem. 2022, 87, 10105-10113. (Abstract)

  • Hu, G.; Brenner-Moyer, S. E.* “Design and synthesis of novel pyrrolidine-bipyridine structures.” Synth. Commun. 2022, 52, 1657-1663. (Abstract)

  • Hu, G.; Brenner-Moyer, S. E.* “Combining palladium and chiral organocatalysis for the enantioselective deconjugative allylation of enals via dienamine intermediates.” J. Org. Chem. 2022, 87, 866-873. (Abstract)

  • Rodríguez-Alvarado, M.; Russo, R.; Connell, N. D.; Brenner-Moyer, S. E.* “Design, organocatalytic synthesis, and bioactivity evaluation of enantiopure fluorinated LpxC inhibitors.” Org. Biomol. Chem. 2020, 18, 5867-5878. (Abstract)

  • Fuhr, K. N.; Hirsch, D. R.; Murelli, R. P.*; Brenner-Moyer, S. E.* “Catalytic enantioselective intermolecular [5+2] dipolar cycloadditions of a 3-hydroxy-4-pyrone-derived oxidopyrylium ylide.” Org. Lett. 2017, 19, 6356-6359. (Abstract)

  • Hu, G.; Ramakumar, K.; Brenner-Moyer, S. E.* “Metal- and O2 free oxidative C-C bond cleavage of aromatic aldehydes.” J. Org. Chem. 2017, 82, 6972–6977. (Abstract)

  • Nareddy, P.; Jordan, F.; Brenner-Moyer, S. E.; Szostak, M.* “Ruthenium(II)-catalyzed regioselective C-H arylation of cyclic and N,N-dialkyl benzamides with boronic acids by weak coordination.” ACS Catal. 2016, 6, 4755-4759. (Abstract)

  • Guo, Q.; Fraboni, A. J.; Brenner-Moyer, S. E.* “Direct diastereo- and enantioselective vinylogous Michael additions of linear enones.” Org. Lett. 2016, 18, 2628-2631. (Abstract)

  • Fraboni, A. J.; Brenner-Moyer, S. E.* “Dienamine-catalyzed nitrone formation via redox reaction.” Org. Lett. 2016, 18, 2146-2149. (Abstract)

  • Hayes, M. D.; Rodríguez-Alvarado, M.; Brenner-Moyer, S. E.* “An organocascade approach to α,α-chlorofluoroalcohols.” Tetrahedron Lett. 2015, 56, 4718-4720. (Abstract)

  • Jones, J. H.; Appayee, C.; Brenner-Moyer, S. E.* “One-pot preparation of enantiopure fluorinated β-amino acid precursors.” Eur. J. Org. Chem. 2014, 2014, 5273-5280. (Abstract)

  • Brenner-Moyer, S. E.; “Carbon-halogen bond formation.” In Stereoselective Organocatalysis: Bond Formation Methodologies and Activation Modes; 1st Ed. Rios Torres, R., Ed. John Wiley & Sons, Inc.: New Jersey, 2013; pp 465-492. (Abstract)

  • Appayee, C.; Fraboni, A. J.; Brenner-Moyer, S. E.* “γ-Amino alcohols via organocascade reactions involving dienamine catalysis.” J. Org. Chem. 2012, 77, 8828-8834. (Abstract)

  • McGarraugh, P. G.; Johnston, R. C.; Martínez-Muñoz, A.; Cheong, P. H.-Y.*; Brenner-Moyer, S. E.* “Organocascade kinetic resolution cascade reactions: New mechanistic and stereochemical manifold in diphenyl prolinol silyl ether catalysis.” Chem. Eur. J. 2012, 18, 10742-10752. (Abstract)

  • McGarraugh, P. G.; Brenner-Moyer, S. E.* “An organocascade kinetic resolution.” Org. Lett. 2011, 13, 6460-6463. (Abstract)

  • McGarraugh, P. G.; Jones, J. H.; Brenner-Moyer, S. E.* “A general organocatalyzed Michael-Michael cascade reaction generates functionalized cyclohexenes.” J. Org. Chem. 2011, 76, 6309-6319. (Abstract)

  • Appayee, C.; Brenner-Moyer, S. E.* “Organocatalytic enantioselective olefin aminofluorination.” Org. Lett. 2010, 12, 3356-3359. (Abstract)

    **Highlighted in Synfacts

  • McGarraugh, P. G.; Brenner, S. E.* “A new organocatalyzed Michael-Michael cascade reaction generates highly substituted fused carbocycles.” Org. Lett. 2009, 11, 5654-5657. (Abstract)

    **Highlighted in Synfacts

  • McGarraugh, P. G.; Brenner, S. E.* “Novel bifunctional bissulfonamides catalyze an enantioselective conjugate addition.” Tetrahedron 2009, 65, 449-455. (Abstract)

     Mentored Publications

  • Wender, P. A.*; Baryza, J. L.; Brenner, S. E.; DeChristopher, B. A.; Loy, B. A.; Schrier, A. J.; Verma, V. A. “Design, synthesis, and evaluation of potent bryostatin analogs that modulate PKC translocation selectivity.” Proc. Natl. Acad. Sci. USA 2011, 108, 6721-6726. (Abstract)

  • Mitchell, C. E. T.; Brenner, S. E.; García-Fortanet, J.; Ley, S. V.* “An efficient, asymmetric organocatalyst-mediated conjugate addition of nitroalkanes to unsaturated cyclic and acyclic ketones.” Org. Biomol. Chem. 2006, 4, 2039-2049. (Abstract)

  • Mitchell, C. E. T.; Brenner, S. E.; Ley, S. V.* “A versatile organocatalyst for the asymmetric conjugate addition of nitroalkanes to enones.” Chem. Commun. 2005, 5346-5348. (Abstract)

  • Stone, J. C.*; Stang, S. L.; Zheng, Y.; Dower, N. A.; Brenner, S. E.; Baryza, J. L.; Wender, P. A. “Synthetic bryostatin analogues activate the RasGRP1 signaling pathway.” J. Med. Chem. 2004, 47, 6638-6644. (Abstract)

  • Baryza, J. L.; Brenner, S. E.; Craske, M. L.; Meyer, T.; Wender, P. A.* “Simplified analogs of bryostatin with anti-cancer activity display greater potency for translocation of PKC-δ GFP.” Chem. Biol. 2004, 11, 1261-1267. (Abstract)

  • Wender, P. A.*; Baryza, J. L.; Brenner, S. E.; Clarke, M. O.; Craske, M. L.; Horan, J. C.; Meyer, T.* “Function oriented synthesis: The design, synthesis, PKC binding, and translocation activity of a new bryostatin analogue.” Curr. Drug. Disc. Tech. 2004, 1, 1-11. (Abstract)

  • Wender, P.A.*; Baryza, J. L.; Brenner, S. E.; Clarke, M. O.; Gamber, G. G.; Horan, J. C.; Jessop, T. C.; Kan, C.; Pattabiraman, K.; Williams, T. J. “Inspirations from nature: New reactions, new therapeutic leads, and new drug delivery systems.” Pure Appl. Chem. 2003, 75, 143-155. (Abstract)

  • Wender, P. A.*; Baryza, J. L.; Bennett, C. E.; Bi, F. C.; Brenner, S. E.; Clarke, M. O.; Horan, J. C.; Kan, C.; Lacôte, E.; Lippa, B.; Nell, P. G.; Turner, T. M. “The practical synthesis of a novel and highly potent analogue of bryostatin.” J. Am. Chem. Soc. 2002, 124, 13648-13649. (Abstract)

  • Brown, H.; Vallabhaneni, S.; Solomon, S.; Mothi, S.; McGarvey, S.; Jackson, T.; Putcha, M.; Brenner, S.; Mate, K.; Cu-Uvin, S. “Attitudes towards prenatal HIV testing and treatment among pregnant women in southern India.” Int. J. STD AIDS 2001, 12, 390-394. (Abstract)