{"id":152,"date":"2018-03-19T17:53:27","date_gmt":"2018-03-19T17:53:27","guid":{"rendered":"http:\/\/sites.rochester.edu\/paradine\/?page_id=152"},"modified":"2026-03-05T16:24:09","modified_gmt":"2026-03-05T21:24:09","slug":"publications","status":"publish","type":"page","link":"https:\/\/sites.rochester.edu\/paradine\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n

* indicates authors contributed equally; \u2020 indicates undergraduate co-author<\/p>\n\n\n\n

O\u2019Neil, S.E.; Monteferrante, O.E.; Stanley, B.M.;\u2020 Paradine, S.M. \u201cGeneration of Polysubstituted Tetrahydrofurans via Urea-Enabled, Pd-Catalyzed Olefin Heteroannulation.\u201d Organic Letters<\/em> 2026<\/strong>, 28<\/em>, ASAP. [Full Text<\/a>]<\/p>\n\n\n

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McNichol, C.P.; Borrego, L.; Ertekin, E.;\u2020 Paradine, S.M. \u201cCatalyst-Controlled, Regiodivergent Aminooxygenation Reactions of Dienes.\u201d Journal of Organic Chemistry<\/em> 2026<\/strong>, 91<\/em>, 749-753. [Full Text<\/a>]<\/p>\n\n\n

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Paradine, S.M. \u201cUreas and their derivatives as ligands in transition metal catalysis.\u201d Tetrahedron<\/em>, 2025<\/strong>, 184<\/em>, 134781. [Full Text<\/a>] invited contribution to special issue in honor of Prof. Eric Jacobsen, 2024 Tetrahedron Prize for Creativity in Organic Chemistry<\/em><\/p>\n\n\n

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Monteferrante, O.E.; Houghtling, K.E.; Kropiwnicki, A.R.;\u2020 Paradine, S.M. \u201cUrea Ligand-Promoted Chainwalking Heteroannulation for the Synthesis of 6- and 7-Membered Azaheterocycles.\u201d Chemistry – A European Journal<\/em>, 2024<\/strong>, e202402587. [Full Text<\/a>]<\/p>\n\n\n

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DeCicco, E.M.; Tlapale-Lara, N.; Paradine, S.M. \u201cIncorporation of Azaheterocycle Functionality in Aerobic, Copper-Catalyzed Alkene Aminooxygenation.\u201d RSC Advances<\/em> 2024<\/strong>, 14<\/em>, 28822-28826. [Full Text<\/a>]<\/p>\n\n\n

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Rodina, D.*; Vaith, J.*; Paradine, S.M. “Ligand Control of Regioselectivity in Palladium-Catalyzed Heteroannulation Reactions of 1,3-Dienes.” Nature Communications<\/em> 2024<\/strong>, 15<\/em>, 5433. DOI: 10.1038\/s41467-024-49803-y [Full Text<\/a>]<\/p>\n\n\n

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Canfield, A.M.; Rodina, D.; Paradine, S.M. “Dienes as Versatile Substrates for Transition Metal-Catalyzed Reactions.” Angewandte Chemie International Edition<\/em> 2024<\/strong>, 63<\/em>, e202401550. DOI: 10.1002\/anie.202401550 [Full Text<\/a>]<\/p>\n\n\n

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McNichol, C.P.*; DeCicco, E.M.*; Canfield, A.M.; Carstairs, D.P.;\u2020 Paradine, S.M. “Copper-Catalyzed, Aerobic Aminooxygenation of Cinnamyl N<\/em>-Alkoxy Carbamates via Substrate-Promoted Catalyst Activation.” ACS Catalysis<\/em> 2023<\/strong>, 13<\/em>, 6568-6573. DOI: 10.1021\/acscatal.3c01431. [Full Text<\/a>]<\/p>\n\n\n

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Houghtling, K.E.; Canfield, A.M.; Paradine, S.M. \u201cConvergent Synthesis of Dihydrobenzofurans via Urea Ligand-Enabled Heteroannulation of o<\/em>-Bromophenols with 1,3-Dienes.\u201d Organic Letters<\/em> 2022<\/strong>, 24<\/em>, 5787-5790. [Full Text<\/a>]<\/p>\n\n\n

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Vaith, J.; Rodina, D.; Spaulding, G.S.; Paradine, S.M. “Pd-Catalyzed Heteroannulation Using N<\/em>-Arylureas as a Sterically Undemanding Ligand Platform.” Journal of the American Chemical Society<\/em> 2022<\/strong>, 144<\/em>, 6667\u20136673. DOI: 10.1021\/jacs.2c01019 [Full Text<\/a>]<\/p>\n\n\n

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Prior to Rochester:<\/span><\/span><\/h3>\n

Ronchi, E.*; Paradine, S.M.*;<\/strong> Jacobsen, E.N. \u201cEnantioselective, multicomponent synthesis of homoallylic amines enabled by hydrogen bonding and dispersive interactions.\u201d Journal of the American Chemical Society<\/em>\u00a02021<\/strong>, 143<\/em>, 7272-7278. [Full Text<\/a>]<\/p>\n

Paradine, S.M.*<\/b>; Griffin, J.R.*; Zhao, J.; Petronico, A.L.; Miller, S.; White, M.C. \u201cA Manganese Catalyst for Highly Reactive yet Selective Intramolecular C(sp3<\/span><\/sup>)\u2013<\/span>H Amination.\u201d Nature Chemistry<\/em>, 2015<\/strong>, 7, 987-994.\u00a0<\/span><\/b>[Full Text]<\/a><\/span><\/p>\n

Paradine, S.M.<\/b>; White, M.C. \u201cIron-Catalyzed Intramolecular Allylic C\u2013<\/span>H Amination.\u201d Journal of the American Chemical Society<\/em>, 2012<\/strong>, 134, 2036-2039.\u00a0[Full Text]<\/a><\/span><\/p>\n

Altermann, S.M.; Richardson, R.D.; Page, T.K.; Schmidt, R.K.; Holland, E.; Mohammed, U.; Paradine, S.M.<\/strong>; French, A.N.; Richter, C.; Bahar, A.M.; Witulski, B.; Wirth, T. \u201cCatalytic Enantioselective \u03b1-Oxysulfonylation of Ketones Mediated by Iodoarenes.\u201d <\/span>European Journal of Organic Chemistry<\/span><\/em>, 2008<\/strong><\/span>, <\/span>5315-5328.<\/span>\u00a0[Full Text]<\/a><\/span><\/p>\n

Richardson, R.D.; Page, T.K.; Altermann, S.; <\/span>Paradine, S.M.<\/span><\/strong>; <\/span>French, A.N.; Wirth, T. \u201cEnantioselective \u03b1-Oxytosylation of Ketones Catalysed by Iodoarenes.\u201d <\/span>Synlett<\/span><\/em>, 2007<\/strong><\/span>,<\/span> 538-542.<\/span>\u00a0[Full Text]<\/a><\/span><\/p>\n\n\n

Patents<\/strong><\/h3>\n\n\n\n

White, M.C.; Paradine, S.M.<\/strong>; Griffin, J.R.; Zhao, J.; Petronico, A.L. \u201cGeneral Catalyst for C\u2013H Functionalization.\u201d U.S. Patent 9,770,711, 2017<\/strong>.<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"

* indicates authors contributed equally; \u2020 indicates undergraduate co-author O\u2019Neil, S.E.; Monteferrante, O.E.; Stanley, B.M.;\u2020 Paradine, S.M. \u201cGeneration of Polysubstituted Tetrahydrofurans via Urea-Enabled, Pd-Catalyzed Olefin Heteroannulation.\u201d Organic Letters 2026, 28,…<\/p>\n","protected":false},"author":12,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":"","_members_access_role":[],"_members_access_error":""},"class_list":["post-152","page","type-page","status-publish","hentry"],"acf":{"lead_in":"","display_title":"","subtitle":"","call_to_action":"","hero_image_placement":"no_image","hero_media":"images","hero_pattern_option":"","hero_video":"","hero_image_landing":"","hero_image_landing_two":"","hero_image_landing_three":"","content_modules":null},"yoast_head":"\nPublications - Paradine Research Group<\/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.rochester.edu\/paradine\/publications\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Publications - Paradine Research Group\" \/>\n<meta property=\"og:description\" content=\"* indicates authors contributed equally; 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