{"id":61,"date":"2014-08-03T21:23:06","date_gmt":"2014-08-04T01:23:06","guid":{"rendered":"https:\/\/research.cbc.osu.edu\/nagib.1\/?page_id=61"},"modified":"2026-03-26T12:41:30","modified_gmt":"2026-03-26T16:41:30","slug":"publications","status":"publish","type":"page","link":"https:\/\/research.cbc.osu.edu\/nagib.1\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"61\" class=\"elementor elementor-61\">\n\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-2ef2d8e6 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"2ef2d8e6\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-4752e3d9\" data-id=\"4752e3d9\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-294396b1 elementor-widget elementor-widget-text-editor\" data-id=\"294396b1\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<p style=\"text-align: center;\"><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/myncbi\/david.nagib.1\/bibliography\/public\/\">PubMed<\/a> \u2022 <a href=\"https:\/\/scholar.google.com\/citations?user=t8h1sWIAAAAJ\">Google Scholar<\/a><\/p><table style=\"height: 4000; margin: auto;\"><tbody><tr><td style=\"width: 60px; background: #D8D9D9;\">\u00a0<\/td><td style=\"vertical-align: top; background: #d8d9d9; color: black; font-weight: normal; text-align: center;\"><strong>Key Publications<\/strong> (Graphic Summary):<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\">\u00a0<\/div><div style=\"text-align: left;\"><img fetchpriority=\"high\" decoding=\"async\" class=\"alignnone size-large wp-image-2933\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Research-Summary-2025-new-977x1024.jpeg\" alt=\"\" width=\"960\" height=\"1006\" srcset=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Research-Summary-2025-new-977x1024.jpeg 977w, https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Research-Summary-2025-new-286x300.jpeg 286w, https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Research-Summary-2025-new-768x805.jpeg 768w, https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Research-Summary-2025-new-1466x1536.jpeg 1466w, https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Research-Summary-2025-new-1955x2048.jpeg 1955w, https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Research-Summary-2025-new.jpeg 2018w\" sizes=\"(max-width: 960px) 100vw, 960px\" \/><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Chem-Dec-cover.jpg\" alt=\"\" width=\"57\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/www.cell.com\/chem\/abstract\/S2451-9294(26)00034-3\"> Skeletal editing by iron-catalyzed carbene insertion of trichloromethanes <\/a><br \/><\/strong>Bethany M. DeMuynck,\u2020 Ethan E. Hyland,\u2020 Hojin Kim,\u2020 Victoria L. Menches,\u2020 Anna M. M. Vernier, Zhang Wang, David E. Olson,* Mark D. Levin,*<br \/>and David A. Nagib*<br \/><em>Chem,<\/em> <strong>2026<\/strong>, <em> 389<\/em>, 183\u2013189 (<a href=\"https:\/\/authors.elsevier.com\/a\/1mqdE8jWHEStdN\">open access link<\/a>)<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/TOC-Graphical-Abstract-website.jpeg\" alt=\"\" width=\"400\" height=\"246\" \/><\/div><div>\u00a0<\/div><div style=\"text-align: left;\">\u00a0<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/organic-letters.jpg\" alt=\"\" width=\"57\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.orglett.5c05260\"> Deuterated Cyclopropanation of Alkenes by Iron Catalysis <\/a><br \/><\/strong>Ilias Khan Rana, Khue N. M. Nguyen, Duong T. Ngo, and David A. Nagib<br \/><em>Org. Lett.,<\/em> <strong>2026<\/strong>, <em> 28<\/em>, 1750\u20131754 (<a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.orglett.5c05260\">open access link<\/a>)<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\">\u00a0<\/div><div><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2998 aligncenter\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Deuterocyclopropanation-TOC-1024x709.jpeg\" alt=\"\" width=\"400\" height=\"400\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\">Top 10 <em><a href=\"https:\/\/pubs.acs.org\/action\/showMostReadArticles?journalCode=orlef7\">Most Read Articles<\/a> in OL<\/em>, Feb\/Mar 2026<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/synthesis.jpg\" alt=\"\" width=\"57\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2746-2256\">Iron-Mediated Methyl Esterification with Dibromomethane<\/a><br \/><\/strong> Emma K. Ralph, Bethany M. DeMuynck, and David A. Nagib<br \/><em> Synthesis,<\/em> <strong>2026<\/strong>, DOI: 10.1055\/a-2746-2256<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\">\u00a0<\/div><div><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2998 aligncenter\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Nagib-Esterification-TOC.jpeg\" alt=\"\" width=\"400\" height=\"400\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\">Special Issue: 2025 Women in Chemistry Award to Dr. Dani Schultz<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Science2025.jpg\" alt=\"\" width=\"57\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/www.science.org\/doi\/10.1126\/science.adw4177\"> Harnessing carbene polarity: Unified catalytic access to donor, neutral, and acceptor carbenes <\/a><\/strong><br \/>Khue N. M. Nguyen,\u2020 Xueling Mo,\u2020\u00a0Bethany M. DeMuynck,\u2020\u00a0Mohamed Elsayed, Jacob J. A. Garwood, Duong T. Ngo, Ilias Khan Rana, and David A Nagib<br \/><em>Science,<\/em> <strong>2025<\/strong>, <em> 389<\/em>, 183\u2013189 (<a href=\"https:\/\/www.science.org\/stoken\/author-tokens\/ST-2750\/full\">open access link<\/a>)<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Carbene-Polarity-TOC-1024x420.jpeg\" alt=\"\" width=\"600\" height=\"246\" \/><\/div><div>\u00a0<\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><p><em><a href=\"https:\/\/www.science.org\/doi\/10.1126\/science.adz2592\">Highlighted<\/a>\u00a0in Science<\/em>, &#8220;Electronically diverse carbenes&#8221; by Charette<br \/><em><a href=\"https:\/\/www.cell.com\/chem-catalysis\/abstract\/S2667-1093(25)00291-X\">Highlighted<\/a> in Chem Catalysis<\/em>, &#8220;A universal solution to the carbene electronics conundrum&#8221; by Teeples and Wilkerson-Hill<br \/><em><a href=\"https:\/\/www.chemistryworld.com\/news\/clever-carbene-chemistry-offers-unified-way-to-make-cyclopropanes\/4021937.article\">Highlighted<\/a> in Chemistry World<\/em>, &#8220;Clever carbene chemistry offers unified way to make cyclopropanes&#8221; by Mason Wakley<br \/><em><a href=\"https:\/\/news.osu.edu\/new-chemical-tool-may-improve-development-of-key-drug-components\/\">Highlighted<\/a> in OSU News,<\/em> &#8220;New tools for development of key drugs&#8221; by Tatyana Woodall<\/p><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Chem-Cover.tif.jpg\" alt=\"Chem\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S2667109324003427?dgcid=author\"> Chiral pyrrolidines via an enantioselective Hofmann-L\u00f6ffler-Freytag reaction <\/a><\/strong><br \/>Pavitra Laohapaisan,\u2020 Ipshita Roy,\u2020 and David A. Nagib<br \/><em>Chem Catalysis,<\/em> <strong>2024<\/strong>, <em>4<\/em>, 101149\u2013101158 (<a href=\"https:\/\/authors.elsevier.com\/a\/1jxh-9URZ7rPXZ\">open access<\/a>)<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\">\u00a0<\/div><div style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Chiral-HLF-TOC.jpeg\" alt=\"\" width=\"400\" height=\"399\" \/><\/div><div><em>Featured\u00a0as <a href=\"https:\/\/www.cell.com\/chem-catalysis\/issue?pii=S2667-1093(23)X0013-X#fullCover\">Cover Art<\/a><\/em><em> (Chem Catalysis<\/em>, Vol 4, <a href=\"https:\/\/www.cell.com\/chem-catalysis\/issue?pii=S2667-1093(23)X0013-X#\">Issue 12<\/a>)<\/div><div><em><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2467-4674\">Highlighted<\/a> in Synfacts,<\/em> \u201cEnantioselective, Catalytic HFL Reaction\u201d Dec 2024<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/JACS.gif\" alt=\"\" width=\"57\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.4c06774\"> Radical Polarity<\/a><\/strong><br \/>Jacob J. A. Garwood, Andrew D. Chen, and David A. Nagib<br \/><em> J. Am. Chem. Soc.,<\/em> <strong>2024<\/strong>, <em>146<\/em>, 28034\u201328059<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Radical-Polarity-TOC.jpeg\" alt=\"\" width=\"400\" height=\"170\" \/><\/div><div style=\"text-align: left;\">#1 <em><a href=\"https:\/\/pubs.acs.org\/action\/showMostReadArticles?journalCode=jacsat\">Most Read Article<\/a> in JACS<\/em> for entire year<\/div><div><em><a href=\"https:\/\/www.chemistryworld.com\/news\/new-database-unlocks-predictive-power-of-radical-polarity\/4020355.article\">Highlighted<\/a> in Chemistry World<\/em>, \u201cNew database unlocks predictive power of radical polarity&#8221; by Rupali Dabas<\/div><div><em><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.4c00352\">Highlighted<\/a> in OPRD<\/em>, \u201cSome Items of Interest to Process R&amp;D Chemists and Engineers\u201d <em>Org. Process Res. Dev.<\/em>, 2024, DOI: 10.1021\/acs.oprd.4c00352<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/JACS.gif\" alt=\"\" width=\"57\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.4c07388\"> Cyclopropanation with Non-Stabilized Carbenes via Ketyl Radicals<\/a><\/strong><br \/>Duong T. Ngo \u2020, Jacob J. A. Garwood \u2020, and David A. Nagib<br \/><em> J. Am. Chem. Soc.,<\/em> <strong>2024<\/strong>, <em>146<\/em>, 24009\u201324015<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Ketyl-Cyclopropanation-TOC-1024x586.jpeg\" alt=\"\" width=\"480\" height=\"275\" \/><\/div><div style=\"text-align: left;\"><em>Featured\u00a0as <a href=\"https:\/\/pubs.acs.org\/cms\/10.1021\/jacsat.2024.146.issue-34\/asset\/jacsat.2024.146.issue-34.xlargecover-5.jpg\">cover art<\/a><\/em><em> (JACS<\/em>, Vol 146, <a href=\"https:\/\/pubs.acs.org\/toc\/jacsat\/146\/34\">Issue 34<\/a>)<\/div><div style=\"text-align: left;\">Top 10\u00a0<em><a href=\"https:\/\/pubs.acs.org\/action\/showMostReadArticles?journalCode=jacsat\">Most Read Articles<\/a>\u00a0in JACS<\/em>, Jul\/Aug 2023<\/div><div><em><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.4c00352\">Highlighted<\/a> in OPRD<\/em>, \u201cSome Items of Interest to Process R&amp;D Chemists and Engineers\u201d <em>Org. Process Res. Dev.<\/em>, 2024, DOI: 10.1021\/acs.oprd.4c00352<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Chem-Dec-cover.jpg\" alt=\"Chem\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/www.cell.com\/chem\/fulltext\/S2451-9294(24)00010-X\">Cyclopropanation of unactivated alkenes with non-stabilized iron carbenes<\/a><\/strong><br \/>Bethany M. DeMuynck, Lumin Zhang, Emma K. Ralph, and David A. Nagib<br \/><em>Chem,<\/em> <strong>2024<\/strong>, <em>10<\/em>,\u00a01015\u20131027 (<a href=\"https:\/\/authors.elsevier.com\/a\/1iXM1_tm1kEx8A\">open access<\/a>)<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\">\u00a0<\/div><div style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/TOC-Graphical-Abstract-TOC.jpeg\" alt=\"\" width=\"628\" height=\"250\" \/><\/div><div>\u00a0<\/div><div style=\"text-align: left;\"><em><a href=\"https:\/\/www.chemistryworld.com\/news\/iron-salts-catalyse-the-creation-of-carbenes-for-cyclopropanation\/4018982.article\">Highlighted<\/a>\u00a0in Chemistry World, &#8220;Iron salts catalyse the creation of carbenes for cyclopropanation&#8221; by Fernando Gomoll\u00f3n-Bel<\/em><\/div><div><em><a href=\"https:\/\/www.nature.com\/articles\/s44160-024-00505-9\">Highlighted<\/a> in Nature\u00a0<\/em><i>Synth<\/i><em>esis, &#8220;Cyclopropanes from iron carbenes&#8221; by Peter Seavill<\/em><\/div><div><em><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.4c00127\">Highlighted<\/a> in OPRD<\/em>, \u201cSome Items of Interest to Process R&amp;D Chemists and Engineers\u201d <em>Org. Process Res. Dev.<\/em>, 2024, DOI: 10.1021\/acs.oprd.4c00127<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/6.png\" alt=\"Nature Chemistry\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/www.nature.com\/articles\/s41557-023-01333-8\"> Carbonyl cross-metathesis via deoxygenative gem-di-metal catalysis <\/a><\/strong><br \/>Lumin Zhang and David A. Nagib<br \/><em> Nature Chem.<\/em>, <strong>2024<\/strong>, 16, 107\u2013113 (<a href=\"https:\/\/rdcu.be\/dlRQ2\">open access<\/a>)<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Metathesis-TOC-Graphic-1024x284.png\" alt=\"\" width=\"850\" height=\"236\" \/><\/div><div>\u00a0<\/div><div style=\"text-align: left;\"><em><a href=\"https:\/\/www.chemistryworld.com\/news\/transformative-carbonyl-cross-metathesis-used-to-synthesise-alkenes\/4018110.article\">Highlighted<\/a>\u00a0in Chemistry World, &#8220;\u2018Transformative\u2019 carbonyl cross-metathesis used to synthesise alkenes&#8221; by B\u00e1rbara Pinho<\/em><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/science2022.webp\" alt=\"\" width=\"57\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/www.science.org\/doi\/10.1126\/science.abo6443\">Carbene reactivity from alkyl and aryl aldehydes <\/a><\/strong><br \/>Lumin Zhang, Bethany M. DeMuynck \u2020, Alyson N. Paneque \u2020, Joy E. Rutherford \u2020, and David A. Nagib<br \/><em> Science,<\/em> <strong>2022<\/strong>, <em> 377<\/em>, 649\u2013654<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/TOC-2.png\" alt=\"\" width=\"600\" height=\"254\" \/><\/div><div>\u00a0<\/div><div style=\"text-align: left;\"><em><a href=\"https:\/\/www.science.org\/doi\/10.1126\/science.abq8253\">Highlighted<\/a>\u00a0in Science<\/em>, &#8220;Safe, selective, and scalable carbenes&#8221; by West and Rousseaux<\/div><div><em><a href=\"https:\/\/www.chemistryworld.com\/news\/clever-carbene-synthesis-replaces-notoriously-hazardous-chemistry\/4016067.article\">Highlighted<\/a>\u00a0in Chemistry World,<\/em> &#8220;Carbenes, but without the explosives&#8221; by Kira Welter<\/div><div><em><a href=\"https:\/\/news.osu.edu\/an-easier-and-safer-way-to-synthesize-medicines\/\">Highlighted<\/a>\u00a0in OSU News<\/em>, &#8220;An easier and safer way to synthesize medicines&#8221; by Tatyana Woodall<br \/><em><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.2c00309\">Highlighted<\/a> in OPRD<\/em>, \u201cSome Items of Interest to Process R&amp;D Chemists and Engineers\u201d <em>Org. Process Res. Dev.<\/em>, 2022, 26, 2789<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/JACS.gif\" alt=\"\" width=\"57\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.2c05266\">\u03b3 C\u2013H Functionalization of Amines via Triple H-Atom Transfer of a Vinyl Sulfonyl Radical Chaperone<\/a><\/strong><br \/>James H. Herbort \u2020, Taylor N. Bednar \u2020, Andrew D. Chen, T. V. RajanBabu, and David A. Nagib<br \/><em> J. Am. Chem. Soc.,<\/em> <strong>2022<\/strong>, <em>144<\/em>, 13366\u201313373<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Triple-HAT-TOC-1024x433.jpeg\" alt=\"\" width=\"473\" height=\"200\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\">Top 10\u00a0<em><a href=\"https:\/\/pubs.acs.org\/action\/showMostReadArticles?journalCode=jacsat\">Most Read Articles<\/a>\u00a0in JACS<\/em>, Jul\/Aug 2022<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/ACS-Catalysis-cover.jpg\" alt=\"\" width=\"57\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.2c00804\"> Radical Aza-Heck Cyclization of Imidates via Energy Transfer, Electron Transfer, and Cobalt Catalysis<\/a><\/strong><br \/>Allen F. Prusinowski, Henry C. Sise, Taylor N. Bednar, and David A. Nagib<br \/><em> ACS Catal.,<\/em> <strong>2022<\/strong>, <em>12<\/em>, 4327\u22124332<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/aza-Heck-TOC-1024x249.png\" alt=\"\" width=\"556\" height=\"135\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div>\u00a0<\/div><div style=\"text-align: left;\">Top 5\u00a0<em><a href=\"https:\/\/pubs.acs.org\/action\/showMostReadArticles?journalCode=accacs\">Most Read Articles<\/a>\u00a0in ACS Catalysis<\/em>, Apr 2022<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Chem-Dec-cover.jpg\" alt=\"Chem\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/www.cell.com\/chem\/fulltext\/S2451-9294(21)00528-3\"> Aza-heterocycles via copper-catalyzed, remote C\u2013H desaturation of amines<\/a><\/strong><br \/>Leah M. Stateman \u2020, Ross M. Dare \u2020, Alyson N. Paneque, and David A. Nagib<br \/><em>Chem,<\/em> <strong>2022<\/strong>, <em>8<\/em>, 210\u2013224 (<a href=\"https:\/\/authors.elsevier.com\/a\/1e5I28jWHE9q7Z\">open access<\/a>)<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\">\u00a0<\/div><div style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Desaturation-TOC-horizontal-1024x203.jpeg\" alt=\"\" width=\"756\" height=\"150\" \/><\/div><div>\u00a0<\/div><div style=\"text-align: left;\">\u00a0<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/JACS.gif\" alt=\"JACS\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.1c00886\"> Cross-Selective Aza-Pinacol Coupling via Atom Transfer Catalysis<\/a><\/strong><br \/>Sean M. Rafferty \u2020, Joy E. Rutherford \u2020, Lumin Zhang, Lu Wang, and David A. Nagib<br \/><em>J. Am. Chem. Soc.,<\/em> <strong>2021<\/strong>, <em>143<\/em>, 5622\u20135628<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\">\u00a0<\/div><div style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/aza-pinacol-TOC-1024x295.png\" alt=\"\" width=\"450\" height=\"130\" \/><\/div><div>\u00a0<\/div><div style=\"text-align: left;\">Top 5\u00a0<em><a href=\"https:\/\/pubs.acs.org\/action\/showMostReadArticles?journalCode=jacsat\">Most Read Articles<\/a>\u00a0in JACS<\/em>, Apr\/May 2021<\/div><div style=\"text-align: left;\"><em><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.1c00300\">Highlighted<\/a> in OPRD,<\/em> \u201cSome Items of Interest to Process R&amp;D Chemists and Engineers\u201d Org. Process Res. Dev., <strong>2021<\/strong>, <em>25<\/em>, 1701<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/ACS-Catalysis-cover.jpg\" alt=\"\" width=\"57\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acscatal.1c00404\"> Regioselective Radical Amino-Functionalizations of Allyl Alcohols via Dual Catalytic Cross-Coupling<\/a><\/strong><br \/>Zuxiao Zhang, Duong T. Ngo, and David A. Nagib<br \/><em> ACS Catal.,<\/em> <strong>2021<\/strong>, <em>11<\/em>, 3473\u22123477<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/carboamination-TOC-1024x269.png\" alt=\"\" width=\"450\" height=\"118\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div>Top 5\u00a0<em><a href=\"https:\/\/pubs.acs.org\/action\/showMostReadArticles?topArticlesType=month&amp;journalCode=accacs\">Most Read Articles<\/a>\u00a0in ACS Catalysis<\/em>, Mar\/Apr 2021<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/6.png\" alt=\"Nature Chemistry\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/www.nature.com\/articles\/s41557-020-0482-8\">Enantioselective Radical C\u2013H Amination for the Synthesis of \u03b2-Amino Alcohols<\/a><\/strong><br \/>Kohki M. Nakafuku \u2020, Zuxiao Zhang \u2020, Ethan A. Wappes \u2020, Leah M. Stateman, Andrew D. Chen, and David A. Nagib<br \/><em>Nature Chem.,<\/em> <strong>2020<\/strong>, <em>12<\/em>, 697\u2013704 (<a href=\"https:\/\/rdcu.be\/b46tX\">open access<\/a>)<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\">\u00a0<\/div><div style=\"text-align: left;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/TOC-Nat-Chem-1024x379.png\" alt=\"\" width=\"400\" height=\"148\" \/><\/div><div style=\"text-align: left;\"><em><a href=\"https:\/\/news.osu.edu\/turning-alcohol-into-key-ingredients-for-new-medicines\/\">Highlighted<\/a> in<\/em><em>\u00a0OSU News,\u00a0<\/em>&#8220;Turning alcohol into key ingredients for new medicines&#8221; by Laura Arenschield<br \/><em><a href=\"https:\/\/www.youtube.com\/watch?v=woCzdumGlIk\">Featured<\/a> on<\/em><em> Ohio 24\/7 Now,\u00a0<\/em>&#8220;Alcohol &amp; Amino Acids&#8221; by Myles Harris<\/div><div><em><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/html\/10.1055\/s-0040-1706864\">Highlighted<\/a> in<\/em><i> Synfacts<\/i>, &#8220;Synthesis of \u03b2-Amino Alcohols&#8230;&#8221; <em>Synfacts<\/em>, <strong>2020<\/strong>, 16, 1057<\/div><div><em><a href=\"https:\/\/chemistrycommunity.nature.com\/posts\/radical-c-h-amination\">Behind the Paper<\/a> in<\/em><i> Nature\u00a0Chemistry\u00a0Communities<\/i><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/JACS.gif\" alt=\"JACS\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.0c01318\">Vicinal, Double C\u2013H Functionalization of Alcohols via an Imidate Radical-Polar Crossover Cascade<\/a><\/strong><br \/>Allen F. Prusinowski, Raymond K. Twumasi, Ethan A. Wappes, and David A. Nagib<br \/><em>J. Am. Chem. Soc.,<\/em> <strong>2020<\/strong>,\u00a0<em>142<\/em>, 5429\u22125438<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/vicinal-TOC-1024x297.png\" alt=\"\" width=\"350\" height=\"101\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><em><a href=\"http:\/\/pubs.acs.org\/action\/showMostReadArticles?topArticlesType=month&amp;journalCode=jacsat\">Most Read Article<\/a><\/em>\u00a0in <em>JACS<\/em>, Mar\/Apr 2020<br \/><em><a href=\"https:\/\/cen.acs.org\/synthesis\/Adding-two-functional-groups-aliphatic\/98\/i12\">Highlighted<\/a> in<\/em><em>\u00a0C&amp;E News,\u00a0<\/em>&#8220;Adding two functional groups to an aliphatic alcohol in one shot&#8221; by Fernando Gomoll\u00f3n-Bel, <em>C&amp;E News<\/em>, <strong>2020<\/strong>, <em>98<\/em>\u00a0(12), 7<br \/><em><a href=\"https:\/\/www.chemistryviews.org\/details\/news\/11226955\/Double_Functionalization_of_Alcohols.html\">Highlighted<\/a> in<\/em><em> ChemistryViews,\u00a0<\/em>&#8220;Double Functionalization of Alcohols&#8221; Mar 2020<\/div><div><a style=\"font-size: 12px;\" href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2020\/26October.shtm\" target=\"_blank\" rel=\"noopener\"><i>Highlighted<\/i><\/a><span style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: italic;\">\u00a0in Organic Chemistry Portal, Oct 2020<\/span><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/chemsci-cover.jpeg\" alt=\"\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2020\/SC\/C9SC06239D#!divAbstract\">Radical Cascade Synthesis of Azoles via Tandem Hydrogen Atom Transfer<\/a><\/strong><br \/>Andrew D. Chen \u2020, James H. Herbort \u2020, Ethan A. Wappes, Kohki M. Nakafuku, Darsheed N. Mustafa, and David A. Nagib<br \/><em> Chem. Sci.,<\/em> <strong>2020<\/strong>,\u00a0<em>11<\/em>, 2479\u22122486<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/oxazole-1024x288.png\" alt=\"\" width=\"400\" height=\"112\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><span style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: italic;\"><a style=\"font-size: 12px; color: #a31500;\" href=\"https:\/\/www.thieme-connect.de\/products\/ejournals\/abstract\/10.1055\/s-0040-1707667\">Highlighted<\/a>\u00a0in Synfacts<\/span>, &#8220;Radical Cascade Synthesis of Azoles&#8221;\u00a0<span style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: italic;\">Synfacts<\/span><span style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: normal;\">,\u00a0<\/span><strong style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: normal;\">2020<\/strong><span style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: normal;\">,\u00a0<\/span><span style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: italic;\">16<\/span><span style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: normal;\">, 429<\/span><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Chem-Dec-cover.jpg\" alt=\"\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/www.cell.com\/chem\/fulltext\/S2451-9294(19)30427-9\">Chiral Piperidines from Acyclic Amines via Enantioselective, Radical-Mediated \u03b4 C\u2013H Cyanation<\/a><\/strong><br \/>Zuxiao Zhang, Xin Zhang, and David A. Nagib<br \/><em> Chem,<\/em> <strong>2019<\/strong>, <em>5<\/em>, 3127\u22123134\u00a0<span style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: normal;\">\u00a0(<\/span><a href=\"https:\/\/papers.ssrn.com\/sol3\/papers.cfm?abstract_id=3429297\" target=\"_blank\" rel=\"noopener\">Open Access\u00a0Pre-Print<\/a><span style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: normal;\">)<\/span><\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/TOC-website-1-1024x316.png\" alt=\"\" width=\"400\" height=\"123\" \/><\/div><div style=\"text-align: left;\"><em><a href=\"https:\/\/www.cell.com\/chem\/fulltext\/S2451-9294(19)30522-4\">Highlighted<\/a> in Chem,<\/em> &#8220;Copper Interrupts N-Radical Reactivity and Enables Access to Enantiopure Piperidines&#8221; by McMillan and Leonori, <em>Chem<\/em>, <strong>2019<\/strong>, <em>5<\/em>, 3008\u22122010<\/div><div><em><a href=\"https:\/\/news.osu.edu\/a-simpler-way-to-make-some-medicines\/\"> Highlighted<\/a>\u00a0in OSU News<\/em>, &#8220;A simpler way to make some medicines&#8221; by Laura Arenschield<\/div><div><em><a href=\"https:\/\/www.cell.com\/chem\/issue?pii=S2451-9294(18)X0013-8#\"> Featured<\/a>\u00a0as cover art<\/em>, Dec 2019 issue of <em>Chem<\/em><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/JOC-226x300.jpg\" alt=\"\" width=\"57\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.joc.9b02052\">Development of an Imine Chaperone for Selective C\u2013H Functionalization of Alcohols via Radical Relay<\/a><\/strong><br \/>Kohki M. Nakafuku \u2020, Raymond K. Twumasi \u2020, Avassaya Vanitcha \u2020, Ethan A. Wappes, Kayambu Namitharan, Mathieu Bekkaye, and David A. Nagib<br \/><em> J. Org. Chem.,<\/em> <strong>2019<\/strong>, <em>84<\/em>, 13065\u221213072<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/TOC-1.png\" alt=\"\" width=\"400\" height=\"138\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><a style=\"font-size: 12px;\" href=\"https:\/\/pubs.acs.org\/toc\/joceah\/84\/20\" target=\"_blank\" rel=\"noopener\"><i>Featured<\/i><\/a>\u00a0in Special Issue on C-H Bond Functionalization<\/div><div><em><a href=\"https:\/\/pubs.acs.org\/action\/showMostReadArticles?journalCode=joceah\">Most Read Article<\/a>\u00a0in J. Org. Chem.<\/em>, Sept\/Oct 2019<\/div><div>Top 10\u00a0<em><a href=\"https:\/\/pubs.acs.org\/action\/showMostReadArticles?topArticlesType=recent&amp;journalCode=joceah\">Most Read Article<\/a><\/em>\u00a0of the Year, JOC 2019<\/div><div>Awarded\u00a0<em><a href=\"https:\/\/axial.acs.org\/2020\/03\/11\/joc-2020-outstanding-article-award\/\">Outstanding Article of the Year<\/a><\/em>, <em>JOC<\/em> 2020<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/ChemComm-cover.jpeg\" alt=\"\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2019\/CC\/C9CC03498F#!divAbstract\">Multi-component Heteroarene Couplings via Polarity-reversed Radical Cascades<\/a><\/strong><br \/>Jeremy M. Lear \u2020, J. Quentin Buquoi \u2020, Xin Gu, Kui Pan, Darsheed N. Mustafa, and David A. Nagib<br \/><em> Chem. Commun.,<\/em> <strong>2019<\/strong>, <em>55<\/em>, 8820\u22128823<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Polarity-reversal-TOC-2-1024x206.png\" alt=\"\" width=\"400\" height=\"80\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><em><a href=\"https:\/\/pubs.rsc.org\/en\/journals\/articlecollectionlanding?sercode=cc&amp;themeid=098a6b4f-a8eb-4a4c-9b65-588c121493d1\">Featured<\/a><\/em> in 2019\u00a0Emerging Investigators&#8217; Special Issue (<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlepdf\/2019\/cc\/c9cc90270h?page=search\">Profile<\/a>)<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/ACS-Catalysis-cover.jpg\" alt=\"\" width=\"57\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acscatal.9b01580\"> Heteroarene Phosphinylalkylation via a Catalytic, Polarity-Reversing Radical Cascade<\/a><\/strong><br \/>J. Quentin Buquoi \u2020, Jeremy M. Lear \u2020, Xin Gu, and David A. Nagib<br \/><em> ACS Catal.,<\/em> <strong>2019<\/strong>, <em>9<\/em>, 5330\u22125335<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Phosphinylalkylation-TOC-1024x296.png\" alt=\"\" width=\"400\" height=\"115\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div><div><em><a href=\"https:\/\/pubs.acs.org\/action\/showMostReadArticles?journalCode=accacs\">Most Read Article<\/a>\u00a0in ACS Catalysis<\/em>, May\/Jun 2019<\/div><div>Top 20\u00a0<em><a href=\"https:\/\/pubs.acs.org\/action\/showMostReadArticles?topArticlesType=recent&amp;journalCode=accacs\">Most Read Articles<\/a>\u00a0of the year, ACS Catalysis<\/em>, 2019<\/div><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/chemsci-cover.jpeg\" alt=\"\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/sc\/c8sc05685d#!divAbstract\">Catalytic \u03b2 C\u2013H amination via an imidate radical relay<\/a><\/strong><br \/>Leah M. Stateman, Ethan A. Wappes, Kohki M. Nakafuku, Kara M. Edwards, and David A. Nagib<br \/><em> Chem. Sci.,<\/em> <strong>2019<\/strong>, <em>10<\/em>, 2693\u22122699<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/catalysis-TOC-1024x327.png\" alt=\"\" width=\"400\" height=\"128\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><i>\u00a0<em><a href=\"https:\/\/pubs.rsc.org\/en\/journals\/articlecollectionlanding?sercode=sc&amp;themeid=b05e3a45-fb4e-49b6-93be-41559a52053d\">Highlighted<\/a> in Chem. Sci.<\/em><\/i>\u00a0&#8220;Editor\u2019s Choice&#8221; Collection, 2019<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Chem-231x300.jpg\" alt=\"\" width=\"58\" height=\"75\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/www.cell.com\/chem\/fulltext\/S2451-9294(18)30524-2\"> Site-Selective C\u2013H Functionalization of (Hetero)Arenes via Transient, Non-symmetric Iodanes<\/a><\/strong><br \/>Stacy C. Fosu \u2020, Chido M. Hambira \u2020, Andrew D. Chen, James R. Fuchs, and David A. Nagib<br \/><em> Chem,<\/em> <strong>2019<\/strong>, <em>5<\/em>, 417\u2212428 (<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC6481961\/\">Open Access<\/a>)<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/iodane-TOC-1024x361.png\" alt=\"\" width=\"400\" height=\"141\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><em><a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S2451929419300336\">Highlighted<\/a> in Chem,\u00a0<\/em>&#8220;More Than Just Acetates: PhI(OAc)<sub>2<\/sub> Enables C\u2013H Halogenation of Arenes&#8221; by Wengryniuk,\u00a0<em>Chem,<\/em> <strong>2019<\/strong>, <em>5<\/em>, 254\u2013262<\/div><div><em><a href=\"https:\/\/www.cell.com\/i3\/periodic-table-150th\">Highlighted<\/a> in Chem,\u00a0<\/em>&#8220;150th Anniversary of the Periodic Table: Breakthrough Research on Halogens&#8221;<\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/chemsci-cover.jpeg\" alt=\"\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2019\/SC\/C8SC04366C#!divAbstract\">\u03b4 C\u2212H (Hetero)Arylation via Cu-Catalyzed Radical Relay<\/a><\/strong><br \/>Zuxiao Zhang, Leah M. Stateman, and David A. Nagib<br \/><em> Chem. Sci.,<\/em> <strong>2019<\/strong>, <em>10<\/em>,\u00a01207\u22121211<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Delta-arylation-TOC-1024x303.png\" alt=\"\" width=\"400\" height=\"118\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div><em><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/pdf\/10.1055\/s-0037-1611991.pdf\">Highlighted<\/a>\u00a0in Synfacts<\/em>, &#8220;Copper-Catalyzed Remote Arylation&#8221;\u00a0<em>Synfacts<\/em>, <strong>2019<\/strong>,\u00a0<em>15<\/em>, 171<\/div><div><a style=\"font-size: 12px;\" href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2019\/28October.shtm\" target=\"_blank\" rel=\"noopener\"><i>Highlighted<\/i><\/a><span style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: italic;\">\u00a0in Organic Chemistry Portal, Oct 2019<\/span><\/div><div><a style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: normal;\" href=\"https:\/\/pubs.rsc.org\/en\/journals\/articlecollectionlanding?sercode=sc&amp;themeid=14eb3882-5155-4e60-861f-fb64ae72e109\" target=\"_blank\" rel=\"noopener\"><span style=\"font-style: italic;\">Highlighted<\/span><\/a><span style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px; font-style: italic;\">\u00a0in Chem. Sci.,<\/span> <span style=\"font-family: Arial, Helvetica, sans-serif; font-size: 12px;\">&#8220;Most popular 2018-2019 organic chemistry articles&#8221;<\/span><\/div><div><a href=\"https:\/\/scholar.google.com\/scholar?oi=bibs&amp;hl=en&amp;cites=2284491583590304272\"><em>&gt; 100 citations<\/em><\/a><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Science-2018-cover.gif\" alt=\"\" width=\"60\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"http:\/\/science.sciencemag.org\/content\/362\/6411\/225\"> Ketyl radical reactivity via atom transfer catalysis<\/a><\/strong><br \/>Lu Wang, Jeremy M. Lear, Sean M. Rafferty, Stacy C. Fosu and David A. Nagib<br \/><em>Science,<\/em> <strong>2018<\/strong>, <em>362<\/em>, 225\u2212229 (<a href=\"http:\/\/science.sciencemag.org\/cgi\/content\/full\/362\/6411\/225?ijkey=dCCE9ZXxg5E6k&amp;keytype=ref&amp;siteid=sci\">open access<\/a>)<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/ketyl-radicals-1024x456.png\" alt=\"\" width=\"300\" height=\"134\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div><div><em><a href=\"http:\/\/science.sciencemag.org\/content\/sci\/362\/6411\/157.full.pdf\">Highlighted<\/a> in Science,\u00a0<\/em>&#8220;Easy access to elusive radical reactions&#8221; by Blackburn and Roizen,\u00a0<em>Science,<\/em> <strong>2018<\/strong>,\u00a0<em>362<\/em>, 157\u2212158<\/div><div><em><a href=\"https:\/\/cen.acs.org\/synthesis\/catalysis\/Masked-aldehyde-makes-mild-radical\/96\/i42\">Highlighted<\/a> in C&amp;E News,\u00a0<\/em>&#8220;Masked aldehyde makes mild radical reaction possible&#8221; by\u00a0Tien Nguyen, <em>C&amp;E News<\/em>, <strong>2018<\/strong>, <em>96<\/em> (42), 7<\/div><div><em><a href=\"https:\/\/news.osu.edu\/a-new-way-to-create-molecules-for-drug-development\/\">Highlighted<\/a> in OSU News,\u00a0<\/em>&#8220;A new way to create molecules for drug development&#8221; by\u00a0Jeff Grabmeier<\/div><div><em><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.oprd.8b00396\">Highlighted<\/a> in OPRD,\u00a0<\/em>&#8220;Some Items of Interest to Process R&amp;D Chemists and Engineers&#8221; <em>Org. Process Res. Dev.<\/em>, <strong>2018<\/strong>, <em>22<\/em>, 1687<\/div><div><em><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/pdf\/10.1055\/s-0037-1611383.pdf\">Highlighted<\/a>\u00a0in Synfacts<\/em>, &#8220;Iodine Atom Transfer Catalysis via Ketyl Radicals&#8221; <em>Synfacts<\/em>, <strong>2019<\/strong>, <em>15<\/em>, 63<br \/><a href=\"https:\/\/scholar.google.com\/scholar?oi=bibs&amp;hl=en&amp;cites=2284491583590304272\"><em>&gt; 100 citations<\/em><\/a><\/div><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/JACS.gif\" alt=\"JACS\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.8b07578\">Catalytic Alkene Difunctionalization via Imidate Radicals<\/a><\/strong><br \/>Kohki M. Nakafuku \u2020, Stacy C. Fosu \u2020, and David A. Nagib<br \/><em>J. Am. Chem. Soc.,<\/em> <strong>2018<\/strong>, <em>140<\/em>, 11202\u221211205<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/TOC-Imidate-Radicals-1024x331.png\" alt=\"\" width=\"400\" height=\"129\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><em><a href=\"http:\/\/pubs.acs.org\/action\/showMostReadArticles?topArticlesType=month&amp;journalCode=jacsat\">One of the &#8220;Most Read&#8221; articles<\/a>\u00a0in JACS, Aug-Oct 2018.<\/em><\/div><div><div><em><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.8b00320\">Highlighted<\/a> in OPRD, Oct 2018.\u00a0<\/em>&#8220;Some Items of Interest to Process R&amp;D Chemists and Engineers&#8221; <em>Org. Process Res. Dev.<\/em>, <strong>2018<\/strong>, <em>22<\/em>, 1335<\/div><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/chemsci-cover.jpeg\" alt=\"\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2018\/SC\/C8SC01214H#!divAbstract\">\u03b2 C\u2013H di-halogenation via iterative hydrogen atom transfer<\/a><\/strong><br \/>Ethan A. Wappes \u2020, Avassaya Vanitcha \u2020, and David A. Nagib<br \/><em> Chem. Sci.,<\/em> <strong>2018<\/strong>, <em>9<\/em>, 4500\u20134504<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/TOC-1024x287.png\" alt=\"\" width=\"400\" height=\"112\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><div><em><a href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2018\/26November.shtm\">Highlighted<\/a> in Organic Chemistry Portal, Nov 2018<\/em><\/div><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/JACS.gif\" alt=\"nature2011\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.7b05214\">Directed \u03b2 C\u2013H Amination of Alcohols via Radical Relay Chaperones<\/a><\/strong><br \/>Ethan A. Wappes \u2020, Kohki M. Nakafuku \u2020, and David A. Nagib<br \/><em>J. Am. Chem. Soc.,<\/em> <strong>2017<\/strong>,\u00a0<em>139<\/em>, 10204\u201310207<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/ja-2017-05214e_0010.gif\" alt=\"\" width=\"450\" height=\"149\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><em><a href=\"http:\/\/pubs.acs.org\/action\/showMostReadArticles?topArticlesType=month&amp;journalCode=jacsat\">One of the &#8220;Most Read&#8221; articles<\/a>\u00a0in JACS, Aug 2017<\/em><\/div><div style=\"text-align: left;\"><em><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.oprd.7b00286\">Highlighted<\/a> in OPRD<\/em>, Sept 2017.\u00a0&#8220;Some Items of Interest to Process R&amp;D Chemists and Engineers&#8221; <em>Org. Process Res. Dev.<\/em>, <strong>2017<\/strong>, <em>21<\/em>, 1196<\/div><div><div><em><a href=\"https:\/\/go.osu.edu\/synform2\">Highlighted<\/a> in Synform<\/em>,\u00a0Nov 2017<\/div><div style=\"text-align: left;\"><em><a href=\"https:\/\/www.organic-chemistry.org\/abstracts\/lit5\/949.shtm\">Highlighted<\/a>\u00a0(<a href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2018\/24September.shtm\">twice<\/a>) in Organic Chemistry Portal<\/em>, May 2018 and Sept 2018<\/div><div style=\"text-align: left;\"><div><em><a href=\"https:\/\/pubs.acs.org\/page\/jacsat\/vi\/young-investigator2018.html\">Highlighted<\/a> in ACS Select\u00a0&#8220;JACS <\/em>Young Investigators&#8221; virtual issue, Aug 2018<\/div><div><em><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.8b00363\">Highlighted<\/a> in OPRD<\/em>, Dec 2018. &#8220;Green Chemistry Articles of Interest to the Pharmaceutical Industry&#8221;\u00a0<em>Org. Process Res. Dev.<\/em> <strong>2018<\/strong>, <em>22<\/em>, 1699<\/div><div><a href=\"https:\/\/scholar.google.com\/scholar?oi=bibs&amp;hl=en&amp;cites=2284491583590304272\"><em>&gt; 150 citations<\/em><\/a><\/div><\/div><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/ACIE-2016.gif\" width=\"58\" height=\"75\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1002\/anie.201604704\/abstract\">Triiodide-Mediated \u03b4-Amination of Secondary C-H Bonds<\/a><\/strong><br \/>Ethan A. Wappes, Stacy C. Fosu, Trevor C. Chopko, and David A. Nagib<br \/><em>Angew. Chem. Int. Ed.,<\/em> <strong>2016<\/strong>, <em>55<\/em>, 9974\u20139978<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\">\u00a0<\/div><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/triiodideTOC-1024x281.png\" alt=\"\" width=\"638\" height=\"175\" \/><\/div><div style=\"text-align: right;\">\u00a0<\/div><div style=\"text-align: left;\"><em><a href=\"http:\/\/go.osu.edu\/synform\">Highlighted<\/a> in Synform, featured as <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0036-1589246\">cover<\/a> article, Nov 2016<\/em><\/div><div style=\"text-align: left;\"><em><a href=\"http:\/\/www.organic-chemistry.org\/Highlights\/2017\/25September.shtm\">Highlighted<\/a> in Organic Chemistry Portal, Sept 2017<\/em><\/div><div style=\"text-align: left;\"><a href=\"https:\/\/scholar.google.com\/scholar?oi=bibs&amp;hl=en&amp;cites=2284491583590304272\"><em>&gt; 200\u00a0citations<\/em><\/a><\/div><\/td><\/tr><\/tbody><\/table><p style=\"text-align: center;\"><b>Reviews<\/b><\/p><table style=\"height: 4000; margin: auto;\"><tbody><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Synthesis.jpg\" alt=\"\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/html\/10.1055\/s-0036-1591930\">Remote C\u2013H Functionalization via Selective Hydrogen Atom Transfer<\/a><\/strong><br \/>Leah M. Stateman, Kohki M. Nakafuku, and David A. Nagib<br \/><em> Synthesis,<\/em> <strong>2018<\/strong>, <em>50<\/em>, 1569\u20131586<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Synthesis-TOC.gif\" alt=\"\" width=\"400\" height=\"191\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><i>An essential guide to selective C-H functionalization by radicals (for experts\u00a0and beginners alike)<\/i><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/eros.webp\" alt=\"\" width=\"283\" height=\"397\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/047084289X.rn02431\">(<em>Z<\/em>)-N-Phenoxybenzimidoyl Chloride<\/a><\/strong><br \/>Ross M. Dare, and David A. Nagib<br \/><em>Encyclopedia of Reagents for Organic Synthesis (e-EROS),<\/em> <strong>2022<\/strong>, DOI: 10.1002\/047084289X.rn02431<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/Phenoxybenzimidoyl-Chloride.webp\" alt=\"\" width=\"120\" height=\"121\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><i>Explores the many uses of our imidate radical chaperone<\/i><\/div><\/td><\/tr><\/tbody><\/table><p style=\"text-align: center;\"><b>Perspectives &amp;\u00a0<strong>Highlights<\/strong><\/b><\/p><p><a href=\"https:\/\/www.nature.com\/articles\/s41557-022-01109-6\">Radical arenes<\/a><a href=\"https:\/\/www.nature.com\/articles\/s41557-019-0259-0\"><br \/><\/a>Taylor N. Bender and David A. Nagib<br \/><em>Nature Chem.,<\/em> <strong>2023<\/strong>,<em>\u00a0<\/em><em>15<\/em>, 3\u20134<\/p><p><a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.chemrev.2c00622\">Asymmetric Catalysis in Radical Chemistry<\/a><a href=\"https:\/\/www.nature.com\/articles\/s41557-019-0259-0\"><br \/><\/a>David A. Nagib<br \/><em>Chem. Rev.,<\/em> <strong>2022<\/strong>,<em>\u00a0122<\/em>, 15989\u201315992<\/p><p><a href=\"https:\/\/www.nature.com\/articles\/s41557-019-0259-0\">Nitrogen gets radical<\/a><a href=\"https:\/\/www.nature.com\/articles\/s41557-019-0259-0\"><br \/><\/a>David A. Nagib<br \/><em>Nature Chem.,<\/em> <strong>2019<\/strong>,<em>\u00a011<\/em>, 396\u2013398<\/p><p><a href=\"https:\/\/doi.org\/10.1016\/j.trechm.2019.03.014\">Radical Conversion of Acids to Alkenes via Dual Catalysis<\/a><br \/>Allen F. Prusinowski and David A. Nagib<br \/><em>Trends in Chemistry,<\/em> <strong>2019<\/strong>,<em>\u00a01,\u00a0<\/em>452-453<\/p><p><a href=\"https:\/\/doi.org\/10.1002\/anie.201703311\">Catalytic Desymmetrization by C-H Functionalization as a Solution to the Chiral Methyl Problem<\/a><br \/>David A. Nagib<br \/><em>Angew. Chem. Int. Ed.,<\/em> <strong>2017<\/strong>,<em>\u00a056,<\/em> 7354\u20137356<\/p><p><a href=\"http:\/\/www.cell.com\/chem\/fulltext\/S2451-9294(17)30186-9\">Catalytic, Asymmetric Alkylation via Excited-State Iminium Ions<\/a><br \/>David A. Nagib<br \/><em>Chem,<\/em> <strong>2017<\/strong>,<em>\u00a02<\/em>, 616\u2013618<\/p><p><strong>Pre-OSU<\/strong><\/p><table style=\"height: 4000; margin: auto;\"><tbody><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/JACS.gif\" alt=\"nature2011\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><strong><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.6b04204\">Seven Post-Synthetic Covalent Reactions in Tandem Leading to Enzyme-Like Complexity within Metal-Organic Framework Crystals<\/a><\/strong><br \/>Alejandro M. Fracaroli, Peter Siman, David A. Nagib, Mitsuharu Suzuki, Hiroyasu Furukawa, F. Dean Toste, and Omar M. Yaghi<br \/><em>J. Am. Chem. Soc.,<\/em> <strong>2016<\/strong>,\u00a0<em>138<\/em>, 8352\u20138355<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/MOF.png\" alt=\"\" width=\"400\" height=\"159\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div style=\"text-align: left;\"><em><a href=\"http:\/\/www.nature.com\/nnano\/reshigh\/2016\/0816\/full\/nnano.2016.145.html\">Highlighted<\/a>\u00a0in Nature\u00a0Nanotechnology, \u201cEnzyme pretenders\u201d by Bryden Le Bailly, Aug 2016. <\/em><\/div><div style=\"text-align: left;\"><a href=\"https:\/\/scholar.google.com\/scholar?oi=bibs&amp;hl=en&amp;cites=13357741139356435986\"><em>&gt; 150\u00a0citations<\/em><\/a><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/nature2011.jpg\" alt=\"nature2011\" width=\"58\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><a style=\"color: #800000;\" href=\"https:\/\/www.nature.com\/articles\/nature10647\" target=\"_self\" rel=\"noopener noreferrer\">Trifluoromethylation of Arenes and Heteroarenes by Means of Photoredox Catalysis<\/a><br \/>David A. Nagib\u00a0&amp;\u00a0David\u00a0W. C. MacMillan<br \/><em>Nature,<\/em> <strong>2011<\/strong>,\u00a0<em>480<\/em>, 224\u2013228<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/CF3-arene.png\" alt=\"\" width=\"500\" height=\"123\" \/><\/div><div style=\"text-align: left;\">\u00a0<\/div><div><em>Awarded highest ranking of \u201cExceptional\u201d by the <a href=\"https:\/\/f1000.com\/prime\/13411094\">Faculty of 1000<\/a><\/em><\/div><div><em> <a href=\"http:\/\/www.nature.com\/nature\/journal\/v480\/n7376\/full\/480184a.html\">Highlighted<\/a> by Parsons &amp; Buchwald,\u00a0Nature, 2011, 480, 184\u2013185<\/em><br \/><a href=\"https:\/\/scholar.google.com\/citations?view_op=view_citation&amp;hl=en&amp;user=t8h1sWIAAAAJ&amp;citation_for_view=t8h1sWIAAAAJ:u-x6o8ySG0sC\"><em>&gt;1000 citations<\/em><\/a><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/AngewCover2.gif\" alt=\"AngewCover2\" width=\"58\" height=\"75\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><a style=\"color: #800000;\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201101861\" target=\"_self\" rel=\"noopener noreferrer\">Photoredox Catalysis:\u00a0A Mild, Operationally Simple Approach to the Synthesis of \u03b1-Trifluoromethyl Carbonyl Compounds<br \/><\/a>Phong V. Pham, David A. Nagib, David W. C. MacMillan<br \/><em>Angew. Chem. Int. Ed.,<\/em> <strong>2011<\/strong>,<em>\u00a050<\/em>, 6119\u20136122<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\">\u00a0<\/div><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/CF3-ketone.png\" alt=\"\" width=\"400\" height=\"88\" \/><\/div><div style=\"text-align: right;\">\u00a0<\/div><div style=\"text-align: left;\"><p><em><em><br \/>Selected as a \u201cHot Paper\u201d by the editors of ACIE<br \/><\/em><\/em><a href=\"https:\/\/scholar.google.com\/citations?view_op=view_citation&amp;hl=en&amp;user=t8h1sWIAAAAJ&amp;citation_for_view=t8h1sWIAAAAJ:d1gkVwhDpl0C\"><em><em>&gt;400 citations<\/em><\/em><\/a><\/p><\/div><\/td><\/tr><tr><td style=\"width: 60px; background: #D8D9D9;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/JACS.gif\" alt=\"JACS\" width=\"59\" height=\"76\" \/><\/td><td style=\"vertical-align: top; background: #D8D9D9; color: black; font-weight: normal;\"><a style=\"color: #800000;\" href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja9053338\" target=\"_self\" rel=\"noopener noreferrer\">Enantioselective \u03b1-Trifluoromethylation of Aldehydes via Photoredox Organocatalysis<\/a><br \/>David A. Nagib, Mark\u00a0E. Scott, David W. C. MacMillan<br \/><em>J. Am. Chem. Soc.<\/em>, <strong>2009<\/strong>,\u00a0<em>131,<\/em> 10875\u201310877<\/td><\/tr><tr><td colspan=\"2\"><div style=\"margin: auto; text-align: center;\">\u00a0<\/div><div style=\"margin: auto; text-align: center;\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-content\/uploads\/2014\/08\/CF3-aldehyde.jpg\" alt=\"\" width=\"400\" height=\"118\" \/><\/div><div style=\"text-align: right;\">\u00a0<\/div><div style=\"text-align: left;\"><em><br \/>Most downloaded synthetic methods article in JACS for all of 2009<br \/><a href=\"https:\/\/scholar.google.com\/citations?view_op=view_citation&amp;hl=en&amp;user=t8h1sWIAAAAJ&amp;citation_for_view=t8h1sWIAAAAJ:u5HHmVD_uO8C\">&gt;1000\u00a0citations<\/a><br \/><\/em><\/div><div style=\"text-align: left;\">\u00a0<\/div><\/td><\/tr><\/tbody><\/table><p><!-- \/wp:html --><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>PubMed \u2022 Google Scholar \u00a0 Key Publications (Graphic Summary): \u00a0 Skeletal editing by iron-catalyzed carbene insertion of trichloromethanes Bethany M. DeMuynck,\u2020 Ethan E. Hyland,\u2020 Hojin Kim,\u2020 Victoria L. Menches,\u2020 Anna M. M. Vernier, Zhang Wang, David E. Olson,* Mark D. Levin,*and David A. Nagib*Chem, 2026, 389, 183\u2013189 (open access link) \u00a0\u00a0 Deuterated Cyclopropanation of Alkenes [&hellip;]<\/p>\n","protected":false},"author":5,"featured_media":0,"parent":0,"menu_order":5,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-61","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-json\/wp\/v2\/pages\/61","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-json\/wp\/v2\/users\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-json\/wp\/v2\/comments?post=61"}],"version-history":[{"count":626,"href":"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-json\/wp\/v2\/pages\/61\/revisions"}],"predecessor-version":[{"id":3038,"href":"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-json\/wp\/v2\/pages\/61\/revisions\/3038"}],"wp:attachment":[{"href":"https:\/\/research.cbc.osu.edu\/nagib.1\/wp-json\/wp\/v2\/media?parent=61"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}