{"id":10,"date":"2014-07-01T07:49:03","date_gmt":"2014-07-01T07:49:03","guid":{"rendered":"http:\/\/blogs.cardiff.ac.uk\/wirth\/?page_id=10"},"modified":"2026-09-03T13:33:37","modified_gmt":"2026-09-03T13:33:37","slug":"publications","status":"publish","type":"page","link":"https:\/\/blogs.cardiff.ac.uk\/wirth\/publications\/","title":{"rendered":"Publications 2025\u20132026"},"content":{"rendered":"

2025<\/h1>\n

306. Hydrofluoroether Synthesis through One-Pot Anodic Iodoalkoxylation of Alkenes<\/strong>
\nM. Becerra-Ruiz, B. Winterson, E. G. P\u00e9rez, T. Wirth,\u00a0Adv. Synth. Catal.\u00a0<\/em>2025<\/strong>,\u00a0367<\/em>, e202401108. DOI<\/a><\/p>\n

307. B(C6<\/small>F5<\/small>)3<\/small> Catalyzed Regiodivergent Thioetherifications of Alkenes via Thiiranium Intermediates: Experimental and Computational Insights<\/strong>
\nN. Alotaibi, R. Babaahmadi, S. Das, E. Richards, M. Pramanik, T. Wirth, R. L. Melen, Chem. Eur. J. <\/em>2025<\/strong>, 31<\/i>, e202404236. DOI<\/a><\/p>\n

308. Raman Study of Intermediates Formed During the Electrochemical N<\/em>-Nitrosation of Secondary Amines<\/strong>
\nS. Richardson, R. Babaahmadi, L. Edwards, R. Ali, R. L. Melen, D. Roy, T. Wirth, Chem. Meth. <\/em>2025<\/strong>, 5<\/i>, e202400067. DOI<\/a><\/p>\n

309. Synthesis and Reactivity of Six-Membered Cyclic Diaryl \u03bb3<\/small>-Bromanes and \u03bb3<\/small>-Chloranes<\/strong>
\nD. Bhattacherjee, B. M. Kariuki, B. A. Piscelli, R. A. Cormanich, T. Wirth, Angew. <\/em>Chem. Int. Ed. <\/em>2025<\/strong>, 64<\/em>, e202424559. DOI<\/a><\/p>\n

\u00a0 \u00a0 \u00a0 Synthese und Reaktivit\u00e4t sechsgliedriger zyklischer Diaryl<\/span> \u03bb3<\/small><\/span>–<\/span><\/strong>Bromane und<\/span> \u03bb3-<\/small><\/span>Chlorane
\n<\/span><\/strong>\u00a0 \u00a0 \u00a0 D. Bhattacherjee, B. M. Kariuki, B. A. Piscelli, R. A. Cormanich, T. Wirth, <\/span>Angew. <\/em><\/span>Chem. <\/em><\/span>2025<\/strong>, 137<\/em>, e202424559.<\/i><\/span>\u00a0DOI<\/a><\/p>\n

310. Electrochemical Fluorination of Proline Derivatives<\/strong>
\nP. Ryan, D. Bhattacherjee, T. Wirth, L. Hunter, G. Pascali,\u00a0Eur. J. Org. Chem. <\/em>2025<\/strong>, 28<\/em>, e202500264. DOI<\/a><\/p>\n

311. Electrolyte-Controlled Regiodivergent Continuous Flow Electroselenocyclisations<\/strong>
\nS. Arepally, H. Gieman, T. Wirth<\/span>, Angew. <\/em>Chem. Int. Ed. <\/em>2025<\/strong>, 64<\/em>, e202509811. DOI<\/a><\/p>\n

\u00a0 \u00a0 Elektrolytgesteuerte, regiodivergente, kontinuierliche Elektroselenozyklisierungen<\/span><\/strong>
\n<\/span><\/strong>\u00a0 \u00a0 \u00a0 S. Arepally, H. Gieman, T. Wirth, <\/span>Angew. <\/em><\/span>Chem. <\/em><\/span>2025<\/strong>, 137<\/em>, e202509811.<\/i><\/span>\u00a0DOI<\/a><\/p>\n

312. Flow electrochemical oxidation of N<\/i>-nitrosamines to N<\/i>-nitramines<\/strong>
\nR. Ali, K. Matsui, J. \u0160adauskis, A. Catherall, T. Wirth, Chem. Commun. <\/em>2025<\/strong>, 61<\/em>, 13671\u201313674. DOI<\/a><\/p>\n

313. Imidazopyridine substituted cyclic selenonium(IV) salts as chalcogen bond catalyst<\/strong>
\nT. Kuzmera, P. Puylaert, T. Wirth, B. J. Nachtsheim, Chem. Commun. <\/em>2025<\/strong>, 61<\/em>, 14169\u201314172. DOI<\/a><\/p>\n

314. Electrochemical \u237a-C\u2013H Functionalization of Nitramines for Accessing Bifunctional Energetic Heterocycles<\/strong>
\nW.-C. C. Lee, L. F. T. Novaes, R. Ali, T. Wirth, S. Lin, Angew. Chem. Int. Ed. <\/em>2025<\/strong>, 64<\/em>, e202515252. DOI<\/a><\/p>\n

315. Electric-Field-Assisted Organic Synthesis: A New Frontier in Reactivity Control<\/strong>
\nH. Chadwick, G. Cocking, J. Westph\u00e4ling, R. L. Melen, T. Wirth,\u00a0SynOpen <\/em>2025<\/strong>, 9<\/em>, 282\u2013291. DOI<\/a><\/p>\n

2026<\/h1>\n

316. Oxidative Rearrangement of Alkynes to chiral \u03b1-Arylalkanoic Esters
\n<\/strong>R. Alkahtani, J. Westph\u00e4ling, A. Gorecka, R. Babaahmadi, H. Gieman, M. Finance, J. Lorente Martinez, D. Bhattacherjee, R. L. Melen, M.-H. Baik, T. Wirth,\u00a0Chem. Sci.\u00a0<\/em>2026<\/strong>, 17<\/em>, 1318\u20131324. DOI<\/a><\/p>\n

317. Thiol-Free Sulfenylation Redefined: A Single-Atom Transfer Pathway to Symmetrical Di(hetero)arylthioethers via B(C6<\/small><\/span>F5<\/small><\/span>)3<\/small><\/span> Catalysis
\n<\/strong>M. Pramanik, N. Alotaibi, T. Boruah, N. J. Buurma, R. Babaahmadi, T. Wirth, R. L. Melen,\u00a0J. Am. Chem. Soc.\u00a0<\/em>2026<\/strong>, 148<\/em>, 5325\u20135337. DOI<\/a><\/p>\n

318. Revealing the Mechanism of TEMPO-Hypervalent Iodine(III) Oxidation of Alcohols
\n<\/strong>M. Bingham, T. R. Pradhan, D. Bhattacherjee, R. Alkahtani, P. Kavanagh, T. Wirth, P. Dingwall, J. Am. Chem. Soc.\u00a0<\/em>2026<\/strong>, 148<\/em>, 8852\u20138862. DOI<\/a>
\n<\/strong><\/p>\n

319. Electrochemical Regioselective Chalcogenocyclizations of 2-Alkynylbenzamides in Flow<\/strong>
\nH. Gieman,\u00a0<\/span>S. Arepally,<\/span>\u00a0<\/span>T. Wirth<\/span>,\u00a0ChemElectroChem\u00a0<\/em>2026<\/strong>,\u00a013<\/em>, e202500471. DOI<\/a><\/span><\/p>\n

320<\/strong>. Synthesis and Structure of Group 13 POCOP Complexes
\n<\/strong>S. Pahar, T. Wilde, K. Agrawal, N. T. Coles, B. M. Kariuki, D. L. Kays, A. J. Logsdail, T. Wirth, E. Richards, R. L. Melen, Inorg. Chem.<\/em> 2026<\/strong>, 65<\/em>, 8289\u20138300. DOI<\/a><\/p>\n

321. Borane Catalysed Annulative Sulfenylation of Internal Alkynes: Towards the Synthesis and Study of Highly Unsaturated Heterocycles
\n<\/strong>S. Das, M. Pramanik, J. Westph\u00e4ling, A. K. Gupta, T. Wirth, E. Zysman-Colman, N. J. Buurma, M.-H. Baik, R. L. Melen, Chem. Sci.\u00a0<\/em>2026<\/strong>, 17<\/em>, 11682\u201311692.\u00a0DOI<\/a><\/p>\n

322. Numbering-Up Flow Electroreduction of \u03b1,\u03b2-Unsaturated Carbonyls from Gram to Pilot-Relevant Scale
\n<\/strong>T. Boruah, S. Arepally, R. L. Melen, <\/span>T. Wirth<\/span>,\u00a0Org. Process Res. Dev. <\/em>2026<\/strong>, 30<\/em>, 2067\u20132074. DOI<\/a><\/span>
\n<\/strong><\/p>\n

323. Hydrogen bonding interactions in HFIP enabling the cascade synthesis of sulfenylated 2H<\/em>-chromenes<\/strong>
\nD. H.-P. Mak, S. Das, J. Westph\u00e4ling, T. \u00a0Jeans, A. Gorecka, T. Wirth, M. Pramanik, M.-H. Baik, R. L. Melen, Chem. Commun. <\/em>2026<\/strong>,\u00a062<\/em>, 14821\u201314825.\u00a0<\/em>DOI<\/a><\/p>\n

324. Oxidative Flow Electrochemistry: A Platform for Generating Reactive Intermediates and Reaction Control
\n<\/strong>S. Arepally, T. Boruah, R. L. Melen, <\/span>T. Wirth<\/span>,\u00a0Acc. Chem. Res. <\/em>2026<\/strong>, 59,<\/em>\u00a02800\u20132815. DOI<\/a><\/span><\/p>\n

325. Continuous Flow Electrochemical Oxidation of Activated Methylarenes Using O2
\n<\/small><\/span><\/strong>N. Alqahtani, S. Iwai, T. Boruah, R. L. Melen, <\/span><\/small><\/span>T. Wirth<\/span><\/small><\/span>,\u00a0Org. Biomol. Chem.<\/em> 2026<\/strong>, 24<\/em>, 6754\u20136758. DOI<\/a><\/span><\/small><\/span>
\n<\/small><\/span><\/strong><\/p>\n

326. Condensing the Cage: Novel Insights into the Reaction Pathway of Isowurtzitane Cage Formation<\/strong>
\nC. S. Wolfe, P. F. N. Stewart, R. M. Campbell, J. R. White, A. M. Beardah,\u00a0 J. Fellows, T. Wirth, Propellants Explos. Pyrotech.<\/em>\u00a02026<\/strong>, in press<\/em>. DOI<\/a><\/span><\/small><\/span><\/p>\n

<\/h1>\n

 <\/p>\n","protected":false},"excerpt":{"rendered":"

2025 306. Hydrofluoroether Synthesis through One-Pot Anodic Iodoalkoxylation of Alkenes M. Becerra-Ruiz, B. Winterson, E. G. P\u00e9rez, T. Wirth,\u00a0Adv. Synth. Catal.\u00a02025,\u00a0367, e202401108. DOI 307. B(C6F5)3 Catalyzed Regiodivergent Thioetherifications of Alkenes via Thiiranium Intermediates: Experimental and Computational Insights N. Alotaibi, R. Babaahmadi, S. Das, E. Richards, M. Pramanik, T. Wirth, R. L. Melen, Chem. Eur. J. […]<\/p>\n","protected":false},"author":396,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"open","template":"","meta":{"footnotes":""},"class_list":["post-10","page","type-page","status-publish","hentry"],"jetpack_sharing_enabled":true,"jetpack_shortlink":"https:\/\/wp.me\/P4Odwu-a","meta_box":[],"_links":{"self":[{"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/pages\/10","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/users\/396"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/comments?post=10"}],"version-history":[{"count":390,"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/pages\/10\/revisions"}],"predecessor-version":[{"id":2068,"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/pages\/10\/revisions\/2068"}],"wp:attachment":[{"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/media?parent=10"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}