{"id":363,"date":"2020-07-09T16:51:59","date_gmt":"2020-07-09T16:51:59","guid":{"rendered":"http:\/\/sites.rutgers.edu\/stacey-brenner-moyer\/?page_id=363"},"modified":"2026-03-11T16:13:15","modified_gmt":"2026-03-11T16:13:15","slug":"publications","status":"publish","type":"page","link":"https:\/\/sites.rutgers.edu\/stacey-brenner-moyer\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"<ul>\n<li>\n<p class=\"\">Liu, F.; Vicidomini, A.; Brenner-Moyer, S. E.* &#8220;Mild direct remote hydroxylation of enals in air.&#8221;\u00a0<em>J. Org. Chem.\u00a0<\/em><strong>2026<\/strong>,\u00a0<em><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.6c00095\">ASAP<\/a>.\u00a0<\/em><\/p>\n<\/li>\n<li>\n<p class=\"\">Invited commentary:\u00a0\u00a0Brenner-Moyer, S.* &#8220;Building bridged bicyclic scaffolds.&#8221;\u00a0<em>Nat. Synth\u00a0<\/em><strong>2025<\/strong>, <a href=\"https:\/\/rdcu.be\/elElk\">DOI: 10.1038\/s44160-025-00798-4<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Brenner-Moyer, S. E.* &#8220;Cooperative vinylogous enamine and metal catalysis.&#8221; <em>ChemCatChem<\/em>\u00a0<strong>2025<\/strong>,\u00a0<a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/epdf\/10.1002\/cctc.202402046\">e202402046<\/a><em>.<\/em><\/p>\n<\/li>\n<li>\n<p class=\"\">De Oliveira Silva, A.; Masand, S.; Farah, A. O.; Laddusaw, J.; Urbina, K.; Rodr\u00edguez-Alvarado, M.; Lalancette, R.; Cheong, P. H.-Y.*; Brenner-Moyer, S. E.* \u201cOrganocatalytic enantioselective [1,2]-Stevens rearrangement of azetidinium salts.\u201d <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, <em>89<\/em>, 9063-9067. (<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.4c00534\" target=\"_blank\" rel=\"noopener\">Abstract<\/a>)<\/p>\n<p class=\"\">**<em>Highlighted in <\/em><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/pdf\/10.1055\/s-0043-1774980.pdf\" target=\"_blank\" rel=\"noopener\"><em>Synfacts<\/em><\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">De Oliveira Silva, A.; Harper, J. L.; Fuhr, K. N.; Lalancette, R. A.; Cheong, P. H.-Y.*; Brenner-Moyer, S. E.* \u201cDyKAT by DiCat: Stereoconvergent dienamine-catalyzed Claisen rearrangements.\u201d <em>J. Org. Chem. <\/em><strong>2022<\/strong>, <em>87<\/em>, 10105-10113. (<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.2c01079\">Abstract<\/a>)<\/p>\n<\/li>\n<li>\n<p class=\"\">Hu, G.; Brenner-Moyer, S. E.* \u201cDesign and synthesis of novel pyrrolidine-bipyridine structures.\u201d <em>Synth. Commun.<\/em> <strong>2022<\/strong>, <em>52<\/em>, 1657-1663<em>.<\/em> (<a href=\"https:\/\/www.tandfonline.com\/doi\/full\/10.1080\/00397911.2022.2103433\">Abstract<\/a>)<\/p>\n<\/li>\n<li>\n<p class=\"\">Hu, G.; Brenner-Moyer, S. E.* \u201cCombining palladium and chiral organocatalysis for the enantioselective deconjugative allylation of enals via dienamine intermediates.\u201d <em>J. Org. Chem.<\/em> <strong>2022<\/strong>, <em>87<\/em>, 866-873. (<a href=\"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.joc.1c02591\">Abstract<\/a>)<\/p>\n<\/li>\n<li>\n<p class=\"\">Rodr\u00edguez-Alvarado, M.; Russo, R.; Connell, N. D.; Brenner-Moyer, S. E.* \u201cDesign, organocatalytic synthesis, and bioactivity evaluation of enantiopure fluorinated LpxC inhibitors.\u201d <em>Org. Biomol. Chem.<\/em> <strong>2020<\/strong>, <em>18<\/em>, 5867-5878. <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2020\/ob\/d0ob01125h#!divAbstract\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Fuhr, K. N.; Hirsch, D. R.; Murelli, R. P.*; Brenner-Moyer, S. E.* &#8220;Catalytic enantioselective intermolecular [5+2] dipolar cycloadditions of a 3-hydroxy-4-pyrone-derived oxidopyrylium ylide.&#8221; <em>Org. Lett. <\/em><strong>2017<\/strong>, <em>19<\/em>, 6356-6359<em>. <\/em><a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.orglett.7b03196\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Hu, G.; Ramakumar, K.; Brenner-Moyer, S. E.* &#8220;Metal- and O2 free oxidative C-C bond cleavage of aromatic aldehydes.&#8221; <em>J. Org. Chem.<\/em> <strong>2017<\/strong>, <em>82<\/em>, 6972\u20136977. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.joc.7b00784\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Nareddy, P.; Jordan, F.; Brenner-Moyer, S. E.; Szostak, M.* &#8220;Ruthenium(II)-catalyzed regioselective C-H arylation of cyclic and <em>N,N<\/em>-dialkyl benzamides with boronic acids by weak coordination.&#8221; <em>ACS Catal. <\/em><strong>2016<\/strong>, <em>6<\/em>, 4755-4759. <a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acscatal.6b01360\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Guo, Q.; Fraboni, A. J.; Brenner-Moyer, S. E.* &#8220;Direct diastereo- and enantioselective vinylogous Michael additions of linear enones.&#8221; <em>Org. Lett.<\/em> <strong>2016<\/strong>, <em>18<\/em>, 2628-2631. <a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.orglett.6b01050\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Fraboni, A. J.; Brenner-Moyer, S. E.* &#8220;Dienamine-catalyzed nitrone formation via redox reaction.&#8221; <em>Org. Lett.<\/em> <strong>2016<\/strong>, <em>18<\/em>, 2146-2149. <a href=\"#\">(<\/a><a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.orglett.6b00770\" target=\"_blank\" rel=\"noopener\">Abstract<\/a><a href=\"#\">)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Hayes, M. D.; Rodr\u00edguez-Alvarado, M.; Brenner-Moyer, S. E.* &#8220;An organocascade approach to \u03b1,\u03b1-chlorofluoroalcohols.&#8221; <em>Tetrahedron Lett.<\/em> <strong>2015<\/strong>, <em>56<\/em>, 4718-4720. <a href=\"#\">(<\/a><a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403915009491\" target=\"_blank\" rel=\"noopener\">Abstract<\/a><a href=\"#\">)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Jones, J. H.; Appayee, C.; Brenner-Moyer, S. E.* &#8220;One-pot preparation of enantiopure fluorinated \u03b2-amino acid precursors.&#8221; <em>Eur. J. Org. Chem. <\/em><strong>2014<\/strong>, <em>2014<\/em>, 5273-5280. <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ejoc.201402369\/abstract\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Brenner-Moyer, S. E.; &#8220;Carbon-halogen bond formation.&#8221; In <em>Stereoselective Organocatalysis: Bond Formation Methodologies and Activation Modes<\/em>; 1st Ed. Rios Torres, R., Ed. John Wiley &amp; Sons, Inc.: New Jersey, 2013; pp 465-492. <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/9781118604755.ch13\/summary\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Appayee, C.; Fraboni, A. J.; Brenner-Moyer, S. E.* &#8220;\u03b3-Amino alcohols via organocascade reactions involving dienamine catalysis.&#8221; <em>J. Org. Chem.<\/em> <strong>2012<\/strong>, <em>77<\/em>, 8828-8834. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jo3017007\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">McGarraugh, P. G.; Johnston, R. C.; Mart\u00ednez-Mu\u00f1oz, A.; Cheong, P. H.-Y.*; Brenner-Moyer, S. E.* &#8220;Organocascade kinetic resolution cascade reactions: New mechanistic and stereochemical manifold in diphenyl prolinol silyl ether catalysis.&#8221; <em>Chem. Eur. J.<\/em> <strong>2012<\/strong>, <em>18<\/em>, 10742-10752. <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/chem.201104029\/abstract\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">McGarraugh, P. G.; Brenner-Moyer, S. E.* &#8220;An organocascade kinetic resolution.&#8221; <em>Org. Lett. <\/em><strong>2011<\/strong>, <em>13<\/em>, 6460-6463. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol2027587\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">McGarraugh, P. G.; Jones, J. H.; Brenner-Moyer, S. E.* &#8220;A general organocatalyzed Michael-Michael cascade reaction generates functionalized cyclohexenes.&#8221; <em>J. Org. Chem.<\/em> <strong>2011<\/strong>, <em>76<\/em>, 6309-6319. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jo201140a\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Appayee, C.; Brenner-Moyer, S. E.* &#8220;Organocatalytic enantioselective olefin aminofluorination.&#8221; <em>Org. Lett.<\/em> <strong>2010<\/strong>, <em>12<\/em>, 3356-3359. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol101167z\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<p class=\"\"><em> **Highlighted in <\/em><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0030-1257967\" target=\"_blank\" rel=\"noopener\"><em>Synfacts<\/em><\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">McGarraugh, P. G.; Brenner, S. E.* &#8220;A new organocatalyzed Michael-Michael cascade reaction generates highly substituted fused carbocycles.&#8221; <em>Org. Lett.<\/em> <strong>2009<\/strong>, <em>11<\/em>, 5654-5657. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol9024293\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<p class=\"\"><em> **Highlighted in <\/em><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0029-1219132\" target=\"_blank\" rel=\"noopener\"><em>Synfacts<\/em><\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">McGarraugh, P. G.; Brenner, S. E.* &#8220;Novel bifunctional bissulfonamides catalyze an enantioselective conjugate addition.&#8221; <em>Tetrahedron<\/em> <strong>2009<\/strong>, <em>65<\/em>, 449-455. <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402008019662\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<\/ul>\n<p class=\"\"><strong style=\"color: inherit;font-size: 1.44em\">\u00a0 \u00a0 \u00a0Mentored Publications<\/strong><\/p>\n<ul data-rte-list=\"default\" data-pm-slice=\"3 3 []\">\n<li>\n<p class=\"\">Wender, P. A.*; Baryza, J. L.; Brenner, S. E.; DeChristopher, B. A.; Loy, B. A.; Schrier, A. J.; Verma, V. A. &#8220;Design, synthesis, and evaluation of potent bryostatin analogs that modulate PKC translocation selectivity.&#8221; <em>Proc. Natl. Acad. Sci. USA<\/em> <strong>2011<\/strong>, <em>108<\/em>, 6721-6726. <a href=\"http:\/\/www.pnas.org\/content\/108\/17\/6721.abstract?sid=f0dbbfcb-3d49-4860-b8aa-cbe4c5b041fb\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Mitchell, C. E. T.; Brenner, S. E.; Garc\u00eda-Fortanet, J.; Ley, S. V.* &#8220;An efficient, asymmetric organocatalyst-mediated conjugate addition of nitroalkanes to unsaturated cyclic and acyclic ketones.&#8221; <em>Org. Biomol. Chem. <\/em><strong>2006<\/strong>, <em>4<\/em>, 2039-2049. <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2006\/ob\/b601877g#!divAbstract\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Mitchell, C. E. T.; Brenner, S. E.; Ley, S. V.* &#8220;A versatile organocatalyst for the asymmetric conjugate addition of nitroalkanes to enones.&#8221; <em>Chem. Commun. <\/em><strong>2005<\/strong>, 5346-5348. <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2005\/cc\/b511441a#!divAbstract\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Stone, J. C.*; Stang, S. L.; Zheng, Y.; Dower, N. A.; Brenner, S. E.; Baryza, J. L.; Wender, P. A. &#8220;Synthetic bryostatin analogues activate the RasGRP1 signaling pathway.&#8221; <em>J. Med. Chem.<\/em> <strong>2004<\/strong>, <em>47<\/em>, 6638-6644. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jm0495069\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Baryza, J. L.; Brenner, S. E.; Craske, M. L.; Meyer, T.; Wender, P. A.* &#8220;Simplified analogs of bryostatin with anti-cancer activity display greater potency for translocation of PKC-\u03b4 GFP.&#8221; <em>Chem. Biol.<\/em> <strong>2004<\/strong>, <em>11<\/em>, 1261-1267. <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S1074552104002285\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Wender, P. A.*; Baryza, J. L.; Brenner, S. E.; Clarke, M. O.; Craske, M. L.; Horan, J. C.; Meyer, T.* &#8220;Function oriented synthesis: The design, synthesis, PKC binding, and translocation activity of a new bryostatin analogue.&#8221; <em>Curr. Drug. Disc. Tech.<\/em> <strong>2004<\/strong>, <em>1<\/em>, 1-11. <a href=\"http:\/\/benthamscience.com\/journal\/abstracts.php?journalID=cddt&amp;articleID=91090\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">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. &#8220;Inspirations from nature: New reactions, new therapeutic leads, and new drug delivery systems.&#8221; <em>Pure Appl. Chem.<\/em> <strong>2003<\/strong>, <em>75<\/em>, 143-155. <a href=\"http:\/\/www.iupac.org\/publications\/pac\/75\/2\/0143\/\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Wender, P. A.*; Baryza, J. L.; Bennett, C. E.; Bi, F. C.; Brenner, S. E.; Clarke, M. O.; Horan, J. C.; Kan, C.; Lac\u00f4te, E.; Lippa, B.; Nell, P. G.; Turner, T. M. &#8220;The practical synthesis of a novel and highly potent analogue of bryostatin.&#8221; <em>J. Am. Chem. Soc.<\/em> <strong>2002<\/strong>, <em>124<\/em>, 13648-13649. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja027509%2B\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<li>\n<p class=\"\">Brown, H.; Vallabhaneni, S.; Solomon, S.; Mothi, S.; McGarvey, S.; Jackson, T.; Putcha, M.; Brenner, S.; Mate, K.; Cu-Uvin, S. &#8220;Attitudes towards prenatal HIV testing and treatment among pregnant women in southern India.&#8221; <em>Int. J. STD AIDS <\/em><strong>2001<\/strong>, <em>12<\/em>, 390-394. <a href=\"http:\/\/std.sagepub.com\/content\/12\/6\/390.abstract\" target=\"_blank\" rel=\"noopener\">(Abstract)<\/a><\/p>\n<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Liu, F.; Vicidomini, A.; Brenner-Moyer, S. E.* &#8220;Mild direct remote hydroxylation of enals in air.&#8221;\u00a0J. Org. Chem.\u00a02026,\u00a0ASAP.\u00a0 Invited commentary:\u00a0\u00a0Brenner-Moyer, S.* &#8220;Building bridged bicyclic scaffolds.&#8221;\u00a0Nat. Synth\u00a02025, DOI: 10.1038\/s44160-025-00798-4 Brenner-Moyer, S. E.* &hellip; <a href=\"https:\/\/sites.rutgers.edu\/stacey-brenner-moyer\/publications\/\" class=\"\">Read More<\/a><\/p>\n","protected":false},"author":21,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-363","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.5 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Publications - Stacey Brenner-Moyer<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/sites.rutgers.edu\/stacey-brenner-moyer\/publications\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Publications - Stacey Brenner-Moyer\" \/>\n<meta property=\"og:description\" content=\"Liu, F.; Vicidomini, A.; Brenner-Moyer, S. E.* &#8220;Mild direct remote hydroxylation of enals in air.&#8221;\u00a0J. Org. Chem.\u00a02026,\u00a0ASAP.\u00a0 Invited commentary:\u00a0\u00a0Brenner-Moyer, S.* &#8220;Building bridged bicyclic scaffolds.&#8221;\u00a0Nat. Synth\u00a02025, DOI: 10.1038\/s44160-025-00798-4 Brenner-Moyer, S. 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E.* &#8220;Mild direct remote hydroxylation of enals in air.&#8221;\u00a0J. Org. Chem.\u00a02026,\u00a0ASAP.\u00a0 Invited commentary:\u00a0\u00a0Brenner-Moyer, S.* &#8220;Building bridged bicyclic scaffolds.&#8221;\u00a0Nat. Synth\u00a02025, DOI: 10.1038\/s44160-025-00798-4 Brenner-Moyer, S. 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