{"id":82,"date":"2021-11-15T16:00:59","date_gmt":"2021-11-15T16:00:59","guid":{"rendered":"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/?page_id=82"},"modified":"2026-03-11T10:56:37","modified_gmt":"2026-03-11T10:56:37","slug":"publications","status":"publish","type":"page","link":"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n<p><strong>55. Maximizing the benefits of competition: combining CHEMmunicate with post-game quizzes to support undergraduate students\u2019 learning of organic chemistry<\/strong><br>C. Navarro,* M. N. Hopkinson*<br><em>Chem. Teach. Int. <\/em><strong>2026<\/strong>, DOI: 10.1515\/cti-2026-0005.<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"827\" height=\"360\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2026\/03\/Website-TOC.jpg\" alt=\"\" class=\"wp-image-303\" style=\"width:535px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2026\/03\/Website-TOC.jpg 827w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2026\/03\/Website-TOC-300x131.jpg 300w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2026\/03\/Website-TOC-768x334.jpg 768w\" sizes=\"auto, (max-width: 827px) 100vw, 827px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/www.degruyterbrill.com\/document\/doi\/10.1515\/cti-2026-0005\/html\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>54. A General Group Testing Strategy for Discovering Chemical Cooperativity<\/strong><br>P. M. Pfl\u00fcger, F. Katzenburg, F. Sandfort, M. Teders, A. G\u00f3mez-Su\u00e1rez, E. A. Standley, M. N. Hopkinson, C. G. Daniliuc, A. Heuer*, F. Glorius*<br><em>Angew. Chem. Int. Ed. <\/em><strong>2026<\/strong>, <em>65<\/em>, e25278.<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"742\" height=\"172\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2026\/03\/Cooperativity-Screen-TOC.jpg\" alt=\"\" class=\"wp-image-300\" style=\"width:587px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2026\/03\/Cooperativity-Screen-TOC.jpg 742w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2026\/03\/Cooperativity-Screen-TOC-300x70.jpg 300w\" sizes=\"auto, (max-width: 742px) 100vw, 742px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202525278\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>53. A Reductive Mechanochemical Approach Enabling Direct Upcycling of Fluoride from Polytetrafluoroethylene (PTFE) into Fine Chemicals<\/strong><br>M. E. Lowe, B. M. Gallant, N. Davison, M. N. Hopkinson, D. J. Kubicki,* E. Lu,* R. J. Armstrong*<br><em>J. Am. Chem. Soc. <\/em><strong>2025<\/strong>, <em>147<\/em>, 40895\u201340899.<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"631\" height=\"214\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2025\/10\/PTFE-JACS-for-Website.jpg\" alt=\"\" class=\"wp-image-293\" style=\"width:519px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2025\/10\/PTFE-JACS-for-Website.jpg 631w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2025\/10\/PTFE-JACS-for-Website-300x102.jpg 300w\" sizes=\"auto, (max-width: 631px) 100vw, 631px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.5c14052\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>52. Photochemical reduction of acylimidazolium salts<\/strong><br>M. Jakob, N. Bechler, H. Abdelwahab, F. Weber, J. Wasternack, L. Kleebauer, J. P. G\u00f6tze, M. N. Hopkinson*<br><em>Beilstein J. Org. Chem.<\/em>&nbsp;<strong>2025,<\/strong>&nbsp;<em>21,<\/em>&nbsp;1973\u20131983.<br>(Part of the thematic issue \u201cModern radical chemistry\u201d; Guest Editor: Prof. H.-M. Huang).<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"833\" height=\"252\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2025\/09\/BJOC-Acylimid-GA-for-Website.jpg\" alt=\"\" class=\"wp-image-285\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2025\/09\/BJOC-Acylimid-GA-for-Website.jpg 833w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2025\/09\/BJOC-Acylimid-GA-for-Website-300x91.jpg 300w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2025\/09\/BJOC-Acylimid-GA-for-Website-768x232.jpg 768w\" sizes=\"auto, (max-width: 833px) 100vw, 833px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure>\n\n\n\n<p><a href=\"https:\/\/www.beilstein-journals.org\/bjoc\/articles\/21\/153\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>51. C=O Methylenation mediated by organo-alkali metal reagents: metal identity and ligand effects<\/strong><br>X. Yang, N. Davison,* M. E. Lowe, P. G. Waddell, R. J. Armstrong,* C. L. McMullin,* M. N. Hopkinson, E. Lu*<br><em>Chem. Sci. <\/em><strong>2025<\/strong>, <em>16<\/em>, 11151\u201311160.<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"1111\" height=\"847\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2025\/05\/Lu-Chem-Sci-2025-for-website.jpg\" alt=\"\" class=\"wp-image-278\" style=\"width:357px;height:auto\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/sc\/d5sc02313k\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>50. CHEMmunicate: A chemical structure drawing game for building scientific communications skills and enhancing social interactions among first year undergraduate students<\/strong><br>C. Navarro,* M. N. Hopkinson*<br><em>J. Chem. Educ. <\/em><strong>2025<\/strong>, <em>102<\/em>, 1839\u20131847.<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"505\" height=\"373\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2025\/04\/CHEMmunicate-website-image.jpg\" alt=\"\" class=\"wp-image-267\" style=\"width:320px;height:auto\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jchemed.4c00845\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>49. <strong>Dual N-Heterocyclic Carbene\/Photoredox-Catalyzed Coupling of Acyl Fluorides and Alkyl Silanes<\/strong><\/strong><br>M. Jakob, L. Steiner, M. G\u00f6bel, J. P. G\u00f6tze, M. N. Hopkinson*<br><em>ACS Catal.<\/em> <strong>2024<\/strong>, <em>14<\/em>, 17642\u201317653.<\/p>\n\n\n<div class=\"wp-block-image is-resized is-style-default\">\n<figure class=\"aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"985\" height=\"388\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2024\/11\/TOC-Graphic-for-Website-Jakob-ACS-Catal.jpg\" alt=\"\" class=\"wp-image-256\" style=\"width:420px;height:auto\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2024\/11\/TOC-Graphic-for-Website-Jakob-ACS-Catal.jpg 985w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2024\/11\/TOC-Graphic-for-Website-Jakob-ACS-Catal-300x118.jpg 300w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2024\/11\/TOC-Graphic-for-Website-Jakob-ACS-Catal-768x303.jpg 768w\" sizes=\"auto, (max-width: 985px) 100vw, 985px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.4c03103\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity is-style-wide\" \/>\n\n\n\n<p><strong>48. <strong>Direct Synthesis of Acyl Fluorides from Carboxylic Acids using Benzothiazolium Reagents<\/strong><\/strong><br>L. M. Maas,\u2020 A. Haswell,\u2020 R. Hughes, M. N. Hopkinson*<br><em>Beilstein J. Org. Chem.<\/em> <strong>2024<\/strong>, <em>20<\/em>, 921-930. <br>(Part of the thematic issue \u201cOrgano-fluorine Chemistry VI\u201d; Guest Editor: Prof. D. O\u2019Hagan).<\/p>\n\n\n<div class=\"wp-block-image is-resized is-style-default\">\n<figure class=\"aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"756\" height=\"219\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2024\/04\/Acid-Fluorides-BJOC-GA.png\" alt=\"\" class=\"wp-image-235\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2024\/04\/Acid-Fluorides-BJOC-GA.png 756w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2024\/04\/Acid-Fluorides-BJOC-GA-300x87.png 300w\" sizes=\"auto, (max-width: 756px) 100vw, 756px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/www.beilstein-journals.org\/bjoc\/articles\/20\/82\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>47. C\u2212F Bond Insertion: An Emerging Strategy for Constructing Fluorinated Molecules<\/strong><br>A. Garg, A. Haswell, M. N. Hopkinson*<br><em>Chem. Eur. J.<\/em> <strong>2024<\/strong>, <em>30<\/em>, e202304229.<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"489\" height=\"241\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2024\/01\/TOC-for-Website.jpg\" alt=\"\" class=\"wp-image-225\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2024\/01\/TOC-for-Website.jpg 489w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2024\/01\/TOC-for-Website-300x148.jpg 300w\" sizes=\"auto, (max-width: 489px) 100vw, 489px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/chem.202304229\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>46. Catalyst-Free Trifluoromethoxylation of Silyl Enol Ethers and Allyl Silanes with Bis(trifluoromethyl)peroxide<\/strong><br>L. M. Maas, C. Fasting, P. Vo\u00dfnacker, N. Limberg, P. Golz, C. M\u00fcller, S. Riedel,* M. N. Hopkinson*<br><em>Angew. Chem. Int. Ed. <\/em><strong>2024<\/strong>, <em>63<\/em>, e202317770.<br>(Hot Paper)<\/p>\n\n\n<div class=\"wp-block-image is-resized is-style-default\">\n<figure class=\"aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"1021\" height=\"189\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/12\/OCF3-ACIE-TOC.jpg\" alt=\"\" class=\"wp-image-216\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/12\/OCF3-ACIE-TOC.jpg 1021w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/12\/OCF3-ACIE-TOC-300x56.jpg 300w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/12\/OCF3-ACIE-TOC-768x142.jpg 768w\" sizes=\"auto, (max-width: 1021px) 100vw, 1021px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202317770\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p> <strong>45. Deoxygenative Perfluoroalkylthiolation of Carboxylic Acids with Benzothiazolium Reagents<\/strong><br>A. Haswell, M. Tironi, H. Wang, M. N. Hopkinson* <br><em>J. Fluorine Chem.<\/em> <strong>2024<\/strong>, <em>273<\/em>, 110231. <br>(Part of the Special Issue honouring Prof. Dr. Beate Koksch, Freie Universit\u00e4t Berlin \u2013 Recipient of the 2021 American Chemical Society Award for Creative Work in Fluorine Chemistry; Editor: J. Thrasher).<\/p>\n\n\n<div class=\"wp-block-image is-resized is-style-default\">\n<figure class=\"aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"395\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/12\/Haswell-Hopkinson-BTSRF-Esters-JFC-GA-1-1024x395.jpg\" alt=\"\" class=\"wp-image-207\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/12\/Haswell-Hopkinson-BTSRF-Esters-JFC-GA-1-1024x395.jpg 1024w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/12\/Haswell-Hopkinson-BTSRF-Esters-JFC-GA-1-300x116.jpg 300w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/12\/Haswell-Hopkinson-BTSRF-Esters-JFC-GA-1-768x296.jpg 768w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/12\/Haswell-Hopkinson-BTSRF-Esters-JFC-GA-1.jpg 1239w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S002211392300146X?via%3Dihub\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p> <strong>44. Formal Insertion of Alkenes Into C(<em>sp<sup>3<\/sup><\/em>)\u2212F Bonds Mediated by Fluorine-Hydrogen Bonding<\/strong><br>A. Garg, N. J. Gerwien, C. Fasting, A. Charlton, M. N. Hopkinson* <br><em>Angew. Chem. Int. Ed.<\/em> <strong>2023<\/strong>, <em>62<\/em>, e202302860. <br>(Hot Paper)<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"709\" height=\"175\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/04\/TOC-for-Website.png\" alt=\"\" class=\"wp-image-188\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/04\/TOC-for-Website.png 709w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/04\/TOC-for-Website-300x74.png 300w\" sizes=\"auto, (max-width: 709px) 100vw, 709px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202302860\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p> <strong>43. A (TD-)DFT Study on Photo-NHC-Catalysis: Photoenolization\/Diels-Alder Reaction of Acid Fluorides Catalyzed by N-Heterocyclic Carbenes<\/strong><br>A. Mavroskoufis, M. Lohani, M. Weber, M. N. Hopkinson,* J. P. G\u00f6tze* <br><em>Chem. Sci.<\/em> <strong>2023<\/strong>, <em>14<\/em>, 4027-4037.<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"535\" height=\"178\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/toc_scheme_PEDA_TDDFT_Final-small.png\" alt=\"\" class=\"wp-image-165\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/toc_scheme_PEDA_TDDFT_Final-small.png 535w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/toc_scheme_PEDA_TDDFT_Final-small-300x100.png 300w\" sizes=\"auto, (max-width: 535px) 100vw, 535px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2023\/SC\/D2SC04732B\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p> <strong>42. Silver-Catalyzed Nucleophilic Deoxydifluoromethylthiolation of Activated Aliphatic Alcohols with BT-SCF<sub>2<\/sub>H<\/strong><br>M. Tironi, M. N. Hopkinson*<br><em>Eur. J. Org. Chem.<\/em> <strong>2022<\/strong>, e202101557.<\/p>\n\n\n<div class=\"wp-block-image is-resized is-style-default\">\n<figure class=\"aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"217\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2022\/04\/image-3-1024x217.png\" alt=\"\" class=\"wp-image-140\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2022\/04\/image-3-1024x217.png 1024w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2022\/04\/image-3-300x63.png 300w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2022\/04\/image-3-768x163.png 768w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2022\/04\/image-3-1536x325.png 1536w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2022\/04\/image-3-940x198.png 940w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2022\/04\/image-3.png 1824w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><figcaption class=\"wp-element-caption\">Image Credit: Wiley-VCH<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/ejoc.202101557\">Link to Full Text <\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>41. Activation of Tetrahydrofuran with 2-((Fluoroalkyl)thio)Benzothiazolium Reagents<\/strong><br>L. M. Maas, J. R. Schmid, C. Fasting, P. Vo\u00dfnacker, A. Mavroskoufis, M. N. Hopkinson*<br><em>Tetrahedron<\/em> <strong>2021<\/strong>, <em>101<\/em>, 132512. <br>(Part of the article collection &#8220;Fluorine and Chalcogens&#8221;; Guest Editors: E. Magnier &amp; G. Dagousset).<\/p>\n\n\n<div class=\"wp-block-image is-resized is-style-default\">\n<figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/www.bcp.fu-berlin.de\/en\/chemie\/chemie\/forschung\/OrgChem\/hopkinson\/publications\/Publication-41\/TOC-THF-Opening-Tetrahedron.png?width=2000\" alt=\"TOC THF Opening Tetrahedron\" \/><figcaption class=\"wp-element-caption\">Image Credit: Elsevier<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402021007973\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>40. Norrish Type II Reactions of Acyl Azolium Salts<\/strong><br>A. Mavroskoufis, A. Rieck, M. N. Hopkinson*<br><em>Tetrahedron<\/em> <strong>2021<\/strong>, <em>100<\/em>, 132497. <br>(Part of the article collection &#8220;System-Oriented Development of Organocatalysis&#8221;; Guest Editor: H. Ohmiya)<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-large\"><img decoding=\"async\" src=\"https:\/\/ars.els-cdn.com\/content\/image\/1-s2.0-S0040402021007821-ga1_lrg.jpg\" alt=\"Norrish Type II Reactions of Acyl Azolium Salts\" \/><figcaption class=\"wp-element-caption\">Image Credit: Elsevier<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402021007821\">Link to Full Text<\/a> <\/p>\n\n\n\n<p><a href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2022\/12September.shtm\">Featured in Org. Chem. Highlights (12th September 2022)<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>39. Deoxygenative Nucleophilic Difluoromethylselenylation of Carboxylic Acids and Alcohols with BT-SeCF<sub>2<\/sub>H<\/strong><br>M. Tironi, S. Dix, M. N. Hopkinson*<br><em>Org. Chem. Front.<\/em> <strong>2021<\/strong>, <em>8<\/em>, 6026-6031.<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"541\" height=\"127\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/TOC-for-website-3.png\" alt=\"\" class=\"wp-image-173\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/TOC-for-website-3.png 541w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/TOC-for-website-3-300x70.png 300w\" sizes=\"auto, (max-width: 541px) 100vw, 541px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2021\/qo\/d1qo01104a\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>38. Recent advances in the chemistry and applications of N-heterocyclic carbenes<\/strong><br>P. Bellotti, M. Koy, M. N. Hopkinson,* F. Glorius*<br><em>Nat. Rev. Chem.<\/em> <strong>2021<\/strong>, <em>5<\/em>, 711-725.<\/p>\n\n\n<div class=\"wp-block-image is-resized is-style-default\">\n<figure class=\"aligncenter\"><img decoding=\"async\" src=\"https:\/\/media.springernature.com\/lw685\/springer-static\/image\/art%3A10.1038%2Fs41570-021-00321-1\/MediaObjects\/41570_2021_321_Figa_HTML.png\" alt=\"\" \/><figcaption class=\"wp-element-caption\">Image Credit: Springer Nature<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/www.nature.com\/articles\/s41570-021-00321-1\">Link to Full Text<\/a><br><a href=\"https:\/\/rdcu.be\/cBodE\">Free SharedIt-Link<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>37. Radical C-H Trifluoromethoxylation of (Hetero)arenes with Bis(trifluoromethyl)peroxide<br><\/strong>S. Dix, P. Golz, J. R. Schmid, S. Riedel,* M. N. Hopkinson*<br><em>Chem. Eur. J.<\/em> <strong>2021<\/strong>, <em>27<\/em>, 11554-11558.<br>(Hot Paper)<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-large is-resized\"><img decoding=\"async\" src=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/cms\/asset\/cb094249-11c5-45e4-b639-2b2a47623354\/chem202101621-toc-0001-m.jpg\" alt=\"Radical C-H Trifluoromethoxylation of (Hetero)arenes with Bis(trifluoromethyl)peroxide\" style=\"width:508px;height:auto\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/chem.202101621\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>36. Benzothiazolium Salts as Reagents for the Deoxygenative Perfluoroalkylthiolation of Alcohols<\/strong><br>A. Ariamajd,\u2020 N. J. Gerwien,\u2020 B. Schwabe, S. Dix, M. N. Hopkinson*<br><em>Beilstein J. Org. Chem.<\/em> <strong>2021<\/strong>, <em>17<\/em>, 83-88.<br>(Part of the thematic issue &#8220;Organo-fluorine chemistry V&#8221;; Guest Editor: D. O&#8217;Hagan)<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-large is-resized\"><img decoding=\"async\" src=\"https:\/\/www.beilstein-journals.org\/bjoc\/content\/figures\/1860-5397-17-8-graphical-abstract.svg?max-width=550&amp;background=ffffff\" alt=\"Benzothiazolium Salts as Reagents for the Deoxygenative Perfluoroalkylthiolation of Alcohols\" style=\"width:570px;height:auto\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/www.beilstein-journals.org\/bjoc\/articles\/17\/8\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>35. Deoxygenative Tri- and Difluoromethylthiolation of Carboxylic Acids with Benzothiazolium Reagents<\/strong><br>M. Tironi,\u2020 L. M. Maas,\u2020 A. Garg, S. Dix, J. P. G\u00f6tze, M. N. Hopkinson*<br><em>Org. Lett.<\/em> <strong>2020<\/strong>, <em>22<\/em>, 8925-8930.<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-large is-resized\"><img decoding=\"async\" src=\"https:\/\/pubs.acs.org\/cms\/10.1021\/acs.orglett.0c03328\/asset\/images\/medium\/ol0c03328_0005.gif\" alt=\"Deoxygenative Tri- and Difluoromethylthiolation of Carboxylic Acids with Benzothiazolium Reagents\" style=\"width:408px;height:auto\" \/><figcaption class=\"wp-element-caption\">Image Credit: Reprinted with permission from Org. Lett. 2020, DOI: 10.1021\/acs.orglett.0c03328. Copyright 2020 American Chemical Society.<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.0c03328\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>34. Photo-NHC Catalysis: Accessing Ketone Photochemistry with Carboxylic Acid Derivatives<\/strong><br>M. N. Hopkinson,* A. Mavroskoufis<br><em>Synlett<\/em> <strong>2021<\/strong>, <em>32<\/em>, 95-101.<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"349\" height=\"187\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/TOC-for-website.png\" alt=\"\" class=\"wp-image-167\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/TOC-for-website.png 349w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/TOC-for-website-300x161.png 300w\" sizes=\"auto, (max-width: 349px) 100vw, 349px\" \/><figcaption class=\"wp-element-caption\">Image Credit: Thieme<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/www.thieme-connect.de\/products\/ejournals\/abstract\/10.1055\/s-0040-1706472\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>33. Light-Promoted Organocatalysis with N-Heterocyclic Carbenes<br><\/strong>A. Mavroskoufis, M. Jakob, M. N. Hopkinson*<br><em>ChemPhotoChem<\/em> <strong>2020<\/strong>, <em>4<\/em>, 5147-5153.<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"520\" height=\"141\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/TOC-for-website-1.png\" alt=\"\" class=\"wp-image-169\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/TOC-for-website-1.png 520w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/TOC-for-website-1-300x81.png 300w\" sizes=\"auto, (max-width: 520px) 100vw, 520px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/cptc.202000120\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>32. Synthesis of Trifluoromethylthiolated Alkenes and Alkynes<\/strong><br>M. N. Hopkinson<br>In Emerging Fluorinated Motifs: Synthesis, Properties and Applications (Eds. D. Cahard, J.-A. Ma); Wiley-VCH: Weinheim, 2020, Volume 2, Chapter 14.<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-large\"><img decoding=\"async\" src=\"https:\/\/media.wiley.com\/product_data\/coverImage300\/13\/35273468\/3527346813.jpg\" alt=\"Emerging Fluorinated Motifs: Synthesis, Properties and Applications\" \/><figcaption class=\"wp-element-caption\">Image Credit: Wiley-VCH<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/www.wiley.com\/en-us\/Emerging+Fluorinated+Motifs%3A+Synthesis%2C+Properties+and+Applications%2C+2+Volume+Set-p-9783527346813\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>31. N-Heterocyclic Carbene Catalyzed Photoenolization\/Diels-Alder Reaction of Acid Fluorides<\/strong><br>A. Mavroskoufis, K. Rajes, P. Golz, A. Agrawal, V. Ru\u00df, J. P. G\u00f6tze, M. N. Hopkinson*<br><em>Angew. Chem. Int. Ed.<\/em> <strong>2020<\/strong>, <em>59<\/em>, 3190-3194; <em>Angew. Chem.<\/em> <strong>2020<\/strong>, <em>132<\/em>, 3216-3220.<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"537\" height=\"142\" src=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/TOC-for-website-2.png\" alt=\"\" class=\"wp-image-171\" srcset=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/TOC-for-website-2.png 537w, https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/files\/2023\/03\/TOC-for-website-2-300x79.png 300w\" sizes=\"auto, (max-width: 537px) 100vw, 537px\" \/><figcaption class=\"wp-element-caption\">Image Credit: The Authors<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201914456\">Link to Full Text in English<\/a><br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ange.201914456\">Link to Full Text in German<\/a><br><br><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0040-1707451\">Highlighted in &#8220;Synfacts&#8221; (B. List, V. K. Singh, <em>Synfacts<\/em> <strong>2020<\/strong>, <em>16<\/em>, 0584)<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>30. Deoxytrifluoromethylthiolation and Selenylation of Alcohols by using Benzothiazolium Reagents<\/strong><br>S. Dix, M. Jakob, M. N. Hopkinson*<br><em>Chem. Eur. J.<\/em> <strong>2019<\/strong>, <em>25<\/em>, 7635-7639.<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-large\"><img decoding=\"async\" src=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/cms\/asset\/f19c76d4-71b1-4570-bb2a-2d74e46ed4f5\/chem201901607-toc-0001-m.jpg\" alt=\"Deoxytrifluoromethylthiolation and Selenylation of Alcohols using Benzothiazolium Reagents\" \/><figcaption class=\"wp-element-caption\">Image Credit: Wiley-VCH<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/chem.201901607\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>29. An Overview of NHCs<\/strong><br>M. N. Hopkinson, F. Glorius<br>In N-Heterocyclic Carbenes in Organocatalysis (Ed. A. T. Biju); Wiley-VCH: Weinheim, 2019, Chapter 1, p. 1-36.<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-large\"><img decoding=\"async\" src=\"https:\/\/media.wiley.com\/product_data\/coverImage300\/05\/35273431\/3527343105.jpg\" alt=\"N-Heterocyclic Carbenes in Organocatalysis\" \/><figcaption class=\"wp-element-caption\">Image Credit: Wiley-VCH<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/www.wiley.com\/en-us\/N+Heterocyclic+Carbenes+in+Organocatalysis-p-9783527343102\"><\/a><a href=\"https:\/\/www.wiley.com\/en-us\/N+Heterocyclic+Carbenes+in+Organocatalysis-p-9783527343102\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>28. Gold in Photocatalysis<\/strong><br>S. Dix, M. N. Hopkinson<br>In Science of Synthesis: Photocatalysis in Organic Synthesis (Ed. B. K\u00f6nig); Thieme: Stuttgart, (2018), Chapter 9.<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-large\"><img decoding=\"async\" src=\"https:\/\/thieme-webshop.cstatic.io\/thumbnail\/c6\/48\/41\/1626400965\/9783132417021_400x400.jpg\" alt=\"Photocatalysis in Organic Synthesis\" \/><figcaption class=\"wp-element-caption\">Image Credit: Thieme<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/www.thieme.com\/books-main\/chemistry\/product\/5133-science-of-synthesis-photocatalysis-in-organic-synthesis\"><\/a><a href=\"https:\/\/www.thieme.com\/books-main\/chemistry\/product\/5133-science-of-synthesis-photocatalysis-in-organic-synthesis\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>27. A Radical Revolution for Trifluoromethoxylation<\/strong><br>B. Sahoo, M. N. Hopkinson*<br><em>Angew. Chem. Int. Ed. <\/em><strong>2018<\/strong>, <em>57<\/em>, 7942-7944; <em>Angew. Chem.<\/em> <strong>2018<\/strong>, <em>130<\/em>, 8070-8072.<\/p>\n\n\n<div class=\"wp-block-image is-style-default\">\n<figure class=\"aligncenter size-large\"><img decoding=\"async\" src=\"https:\/\/onlinelibrary.wiley.com\/cms\/asset\/a1e12c7a-b3fb-4069-84f2-7925491c2c3d\/anie201804939-toc-0001-m.jpg\" alt=\"A Radical Revolution for Trifluoromethoxylation\" \/><figcaption class=\"wp-element-caption\">Image Credit: Wiley-VCH<\/figcaption><\/figure><\/div>\n\n\n<p><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201804939\"><\/a><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201804939\">Link to Full Text in English<\/a><br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ange.201804939\">Link to Full Text in German<\/a> <\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>Pre-Independent Career (Master, PhD &amp; Postdoc)<\/strong><\/p>\n\n\n\n<p><strong>26. Diverse Visible-Light-Promoted Functionalizations of Benzotriazoles Inspired by Mechanism-Based Luminescence Screening<br><\/strong>M. Teders, A. G\u00f3mez-Su\u00e1rez, L. Pitzer, M. N. Hopkinson, F. Glorius*<br><em>Angew. Chem. Int. Ed. <\/em><strong>2017<\/strong>, <em>56<\/em>, 902-906; <em>Angew. Chem.<\/em> <strong>2017<\/strong>, <em>129<\/em>, 921-925.<br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201609393\"><\/a><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201609393\">Link to Full Text in English<\/a><br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ange.201609393\"><\/a><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ange.201609393\">Link to Full Text in German<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>25. Merging Visible Light Photoredox and Gold Catalysis<br><\/strong>M. N. Hopkinson,* A. Tlahuext-Aca, F. Glorius*<br><em>Acc. Chem. Res.<\/em> <strong>2016<\/strong>, <em>49<\/em>, 2261-2272.<br><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.accounts.6b00351\"><\/a><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.accounts.6b00351\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>24. Oxidative Addition to Gold(I) by Photoredox Catalysis: Straightforward Access to Diverse (C,N)-Cyclometalated Gold(III) Complexes<\/strong><br>A. Tlahuext-Aca, M. N. Hopkinson, C. G. Daniliuc, F. Glorius*<br><em>Chem. Eur. J. <\/em><strong>2016<\/strong>, <em>22<\/em>, 11587-11592.<br>(Very Important Paper)<br><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/chem.201602649\"><\/a><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/chem.201602649\">Link to Full Text<\/a><br><br><a href=\"https:\/\/www.chemistryviews.org\/details\/ezine\/9580391\/Easy_Access_to_Cyclometalated_Gold_Complexes.html\">Highlighted in &#8220;Chemistry Views&#8221;<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>23. Mild Metal-Catalyzed C\u2013H Activation: Examples and Concepts<br><\/strong>T. Gensch, M. N. Hopkinson, F. Glorius,* J. Wencel-Delord*<br><em>Chem. Soc. Rev.<\/em> <strong>2016<\/strong>, <em>45<\/em>, 2900-2936.<br><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2016\/cs\/c6cs00075d#!divAbstract\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>22. Accelerated Discovery in Photocatalysis using a Mechanism-based Screening Method<\/strong><br>M. N. Hopkinson, A. G\u00f3mez-Su\u00e1rez, M. Teders, B. Sahoo, F. Glorius*<br><em>Angew. Chem. Int. Ed. <\/em><strong>2016<\/strong>, <em>55<\/em>, 4361-4366; <em>Angew. Chem.<\/em> <strong>2016<\/strong>, <em>128<\/em>, 4434-4439.<br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201600995\">Link to Full Text in English<\/a><br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ange.201600995\">Link to Full Text in German<\/a><br><br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201602253\">Selected for Front Cover<\/a><br><a href=\"https:\/\/www.science.org\/content\/blog-post\/screening-mechanism-not-products\">Highlighted in &#8220;In the Pipeline&#8221; Blog<\/a><br><a href=\"https:\/\/www.forbes.com\/sites\/samlemonick\/2016\/03\/30\/to-find-useful-reactions-start-with-how-they-happen\/?sh=6e706f417485#1446f9cc45d1#1446f9cc45d1\">Highlighted in &#8220;Forbes&#8221; Magazine<\/a><br><a href=\"https:\/\/cen.acs.org\/articles\/94\/i13\/Mechanism-based-screening-accelerates-photocatalysis.html?type=paidArticleContent\">Highlighted in &#8220;Chemical &amp; Engineering News&#8221;<\/a><br><a href=\"https:\/\/www.chemie.de\/news\/157272\/speed-dating-fuer-den-katalysator.html\">Highlighted in &#8220;chemie.de&#8221;<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>21. Alkyne Difunctionalization by Dual Gold\/Photoredox Catalysis<br><\/strong>A. Tlahuext-Aca, M. N. Hopkinson,\u2020 R. A. Garza-Sanchez,\u2020 F. Glorius*<br><em>Chem. Eur. J.<\/em> <strong>2016<\/strong>, <em>22<\/em>, 5909-5913.<br><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/chem.201600710\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>20. Visible Light-Promoted Trifluoromethylthiolation of Styrenes via Dual Photoredox\/Halide Catalysis<\/strong><br>R. Honeker,\u2020 R. A. Garza-Sanchez,\u2020 M. N. Hopkinson,* F. Glorius*<br><em>Chem. Eur. J.<\/em> <strong>2016<\/strong>, <em>22<\/em>, 4395-4399.<br>(Hot Paper)<br><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/chem.201600190\">Link to Full Text<\/a><br><br><a href=\"https:\/\/www.chemistryviews.org\/details\/ezine\/9056691\/Dual_PhotoredoxHalide_Catalysis.html\">Highlighted in &#8220;Chemistry Views&#8221;<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>19. Dual Gold\/Photoredox-Catalyzed C(sp)\u2212H Arylation of Terminal Alkynes with Diazonium Salts<\/strong><br>A. Tlahuext-Aca,\u2020 M. N. Hopkinson,\u2020 B. Sahoo, F. Glorius*<br><em>Chem. Sci.<\/em> <strong>2015<\/strong>, <em>7<\/em>, 89-93.<br><a href=\"https:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2016\/SC\/C5SC02583D#!divAbstract\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>18. External-Photocatalyst-Free Visible-Light-Mediated Synthesis of Indolizines<br><\/strong>B. Sahoo,\u2020 M. N. Hopkinson,\u2020 F. Glorius*<br><em>Angew. Chem. Int. Ed.<\/em> <strong>2015<\/strong>, <em>54<\/em>, 15545-15549; <em>Angew. Chem.<\/em> <strong>2015<\/strong>, <em>127<\/em>, 15766-15770.<br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201506868\">Link to Full Text in English<\/a><br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ange.201506868\">Link to Full Text in German<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>17. Dual Photoredox and Gold Catalysis: Intermolecular Multicomponent Oxyarylation of Alkenes<\/strong><br>M. N. Hopkinson, B. Sahoo, F. Glorius*<br><em>Adv. Synth. Catal.<\/em> <strong>2014<\/strong>, <em>356<\/em>, 2794-2800.<br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/adsc.201400580\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>16. An Overview of N-Heterocyclic Carbenes<br><\/strong>M. N. Hopkinson, C. Richter, M. Schedler, F. Glorius*<br><em>Nature<\/em> <strong>2014<\/strong>, <em>510<\/em>, 485-496.<br><a href=\"https:\/\/www.nature.com\/articles\/nature13384\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>15. Using Rh(III)-Catalyzed C\u2212H Activation as a Tool for the Selective Functionalization of Ketone-Containing Molecules<\/strong><br>M. Boultadakis-Arapinis, M. N. Hopkinson, F. Glorius*<br><em>Org. Lett.<\/em><strong> 2014<\/strong>, <em>16<\/em>, 1630-1633.<br><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol500258q\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>14. Dual Catalysis sees the Light: Combining Photoredox with Organo-, Acid and Transition Metal Catalysis<\/strong><br>M. N. Hopkinson,\u2020 B. Sahoo,\u2020 J.-L. Li, F. Glorius*<br><em>Chem. Eur. J. <\/em><strong>2014<\/strong>, <em>20<\/em>, 3874-3886.<br><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/chem.201304823\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>13. Combining Gold and Photoredox Catalysis: Visible Light-Mediated Oxy- and Aminoarylation of Alkenes<\/strong><br>B. Sahoo, M. N. Hopkinson, F. Glorius*<br><em>J. Am. Chem. Soc. <\/em><strong>2013<\/strong>, <em>135<\/em>, 5505-5508.<br><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja400311h\">Link to Full Text<\/a><br><br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/nadc.201390196\">Highlighted in &#8220;Nachrichten aus der Chemie&#8221;<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>12. Beyond Directing Groups: Transition Metal-Catalyzed C\u2013H Activation of Simple Arenes<\/strong><br>N. Kuhl, M. N. Hopkinson, J. Wencel-Delord, F. Glorius*<br><em>Angew. Chem. Int. Ed.<\/em> <strong>2012<\/strong>, <em>51<\/em>, 10236-10254; <em>Angew. Chem. <\/em><strong>2012<\/strong>, <em>124<\/em>, 10382-10401.<br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201203269\">Link to Full Text in English<\/a><br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ange.201203269\">Link to Full Text in German<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>11. Selective Rh(III)-Catalyzed Cross-Dehydrogenative Coupling of Furan and Thiophene Derivatives<\/strong><br>N. Kuhl, M. N. Hopkinson, F. Glorius*<br><em>Angew. Chem. Int. Ed. <\/em><strong>2012<\/strong>, <em>51<\/em>, 8230-8234; <em>Angew. Chem.<\/em> <strong>2012<\/strong>, <em>124<\/em>, 8354-8358.<br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201203792\">Link to Full Text in English<\/a><br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ange.201203792\">Link to Full Text in German<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>10. Metal-Free Oxidative Fluorination of Phenols with [<sup>18<\/sup>F]Fluoride<br><\/strong>Z. Gao, Y. H. Lim, M. Tredwell, L. Li, S. Verhoog, M. Hopkinson, W. Kaluza, T. L. Collier, J. Passchier, M. Huiban, V. Gouverneur*<br><em>Angew. Chem. Int. Ed.<\/em> <strong>2012<\/strong>, <em>51<\/em>, 6733-6737; <em>Angew. Chem.<\/em> <strong>2012<\/strong>, <em>124<\/em>, 6837-6841.<br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201201502\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>9. Gold-Catalyzed Coupling Reactions<br><\/strong>M. N. Hopkinson, V. Gouverneur<br>Science of Synthesis Knowledge Updates; Thieme: Stuttgart, (2011), Vol. 2011\/2, Section 3.6.13, p101.<br><a href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-103-00039\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>8. Au<sup>I<\/sup>\/Au<sup>III<\/sup> Catalysis: An Alternative Approach for C\u2212C Oxidative Coupling<\/strong><br>M. N. Hopkinson,* A. D. Gee, V. Gouverneur*<br><em>Chem. Eur. J.<\/em> <strong>2011<\/strong>, <em>17<\/em>, 8248-8262.<br><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/chem.201100736\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>7. Palladium-Catalyzed Allylic Fluorination<\/strong><br>C. Hollingworth, A. Hazari, M. N. Hopkinson, M. Tredwell, E. Benedetto, M. Huiban, A. D. Gee, J. M. Brown,* V. Gouverneur*<br><em>Angew. Chem. Int. Ed.<\/em> <strong>2011<\/strong>, <em>50<\/em>, 2613-2617; <em>Angew. Chem.<\/em> <strong>2011<\/strong>, <em>123<\/em>, 2661-2665.<br>(Hot Paper)<br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201007307\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>6. Convergent <sup>18<\/sup>F Radiosynthesis: A New Dimension for Radiolabelling<br><\/strong>L. Li, M. N. Hopkinson, R. Leuma Yona, R. Bejot, A. D. Gee, V. Gouverneur*<br><em>Chem. Sci.<\/em> <strong>2011<\/strong>, <em>2<\/em>, 123-131.<br><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2011\/sc\/c0sc00362j#!divAbstract\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>5. Gold Catalysis and Fluorine<br><\/strong>M. N. Hopkinson, A. D. Gee, V. Gouverneur*<br><em>Isr. J. Chem. <\/em><strong>2010<\/strong>, <em>50<\/em>, 675-690.<br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ijch.201000078\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>4. Gold-Catalyzed Cascade Cyclization-Oxidative Alkynylation of Allenoates<br><\/strong>M. N. Hopkinson, J. E. Ross, G. T. Giuffredi, A. D. Gee, V. Gouverneur*<br><em>Org. Lett.<\/em> <strong>2010<\/strong>, <em>12<\/em>, 4904-4907.<br><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol102061k?journalCode=orlef7&amp;quickLinkVolume=12&amp;quickLinkPage=4904&amp;selectedTab=citation&amp;volume=12\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>3. Gold-Catalyzed Diastereoselective Synthesis of \u03b1-Fluoroenones from Propargyl Acetates<br><\/strong>M. N. Hopkinson, G. T. Giuffredi, A. D. Gee, V. Gouverneur*<br><em>Synlett<\/em> <strong>2010<\/strong>, 2737-2742.<br><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0030-1258992\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>2. Gold-Catalyzed Intramolecular Oxidative Cross-Coupling of Non-Activated Arenes<br><\/strong>M. N. Hopkinson, A. Tessier, A. Salisbury, G. T. Giuffredi, L. E. Combettes, A. D. Gee, V. Gouverneur*<br><em>Chem. Eur. J. <\/em><strong>2010<\/strong>, <em>16<\/em>, 4739-4743.<br><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/chem.201000322\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p><strong>1. Diastereoselective Fluorination of Silylated 1,2-Oxazines to Access Fluorinated N,O-Heterocycles<\/strong><br>Y.-h. Lam, M. N. Hopkinson, S. J. Stanway, V. Gouverneur*<br><em>Synlett <\/em><strong>2007<\/strong>, 3022-3026.<br><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-2007-992361\">Link to Full Text<\/a><\/p>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-wide\" \/>\n\n\n\n<p class=\"has-text-align-center\"><em>\u2020 Denotes joint authorship. * Denotes corresponding authorship.<\/em><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>55. Maximizing the benefits of competition: combining CHEMmunicate with post-game quizzes to support undergraduate students\u2019 learning of organic chemistryC. Navarro,* M. N. Hopkinson*Chem. Teach. Int. 2026, DOI: 10.1515\/cti-2026-0005. Link to Full Text 54. A General Group Testing Strategy for Discovering &hellip; <a href=\"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/publications\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":10607,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-82","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/wp-json\/wp\/v2\/pages\/82","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/wp-json\/wp\/v2\/users\/10607"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/wp-json\/wp\/v2\/comments?post=82"}],"version-history":[{"count":57,"href":"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/wp-json\/wp\/v2\/pages\/82\/revisions"}],"predecessor-version":[{"id":304,"href":"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/wp-json\/wp\/v2\/pages\/82\/revisions\/304"}],"wp:attachment":[{"href":"https:\/\/blogs.ncl.ac.uk\/matthewhopkinson\/wp-json\/wp\/v2\/media?parent=82"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}