Professor Thomas Wirth

Articles

• Boruah, T., Ishizeki, R., Roldan, A., Melen, R. L. and Wirth, T. 2024. Flow electrosynthesis of phosphinamides and phosphoramidates through P–N coupling †. Green Chemistry (10.1039/d4gc04450a)
• Becerra-Ruiz, M., Winterson, B., Pérez, E. and Wirth, T. 2024. Hydrofluoroether synthesis through one‐pot anodic iodoalkoxylation of alkenes. Advanced Synthesis & Catalysis (10.1002/adsc.202401108)
• Patra, T., Arepally, S., Seitz, J. and Wirth, T. 2024. Electrocatalytic continuous flow chlorinations with iodine(I/III) mediators. Nature Communications 15(1), article number: 6329. (10.1038/s41467-024-50643-z)
• Pramanik, M., Das, S., Babaahmadi, R., Pahar, S., Wirth, T., Richards, E. and Melen, R. L. 2024. B(C6F5)3-catalyzed selective C-H chalcogenation of arenes and heteroarenes. Chem (10.1016/j.chempr.2024.05.025)
• Edwards, L., Kariuki, B. M., Didsbury, M., Jones, C. D. and Wirth, T. 2024. Deville rebooted – practical N 2 O 5 synthesis †. Chemical Communications 60(46), pp. 5920-5923. (10.1039/d4cc01403k)
• Alzaidi, O. and Wirth, T. 2024. Continuous flow electroselenocyclization of allylamides and Unsaturated Oximes to selenofunctionalized oxazolines and isoxazolines. ACS Organic & Inorganic Au 4(3), pp. 350-355. (10.1021/acsorginorgau.4c00008)
• Pahar, S., van Ingen, Y., Babaahmadi, R., Kariuki, B. M., Wirth, T., Richards, E. and Melen, R. L. 2024. Diverse reactivity of amidinate-supported boron centers with the hypersilyl anion and access to a monomeric secondary boron hydride. Inorganic Chemistry 63(18), pp. 8302–8311. (10.1021/acs.inorgchem.4c00612)
• Ali, R., Wolfe, C. S. and Wirth, T. 2024. Non‐conventional methodologies for the synthesis of N‐Nntrosamines. Chemistry ‐ Methods 4(4), article number: e202300053. (10.1002/cmtd.202300053)
• Mizar, P., Arepally, S. and Wirth, T. 2024. Biphasic organic synthesis with continuous electro-flow. Current Opinion in Green and Sustainable Chemistry 46, article number: 100896. (10.1016/j.cogsc.2024.100896)
• Alotaibi, N. et al. 2024. B(C6F5)3-catalysed alkylation of imidazo[1,2-a]pyridines using α,β-unsaturated ketones. European Journal of Organic Chemistry 27(12), article number: e202400022. (10.1002/ejoc.202400022)
• Guerzoni, M. G., van Ingen, Y., Babaahmadi, R., Wirth, T., Richards, E. and Melen, R. L. 2024. An un-forgotten classic: the nitro-Mannich reaction between nitrones and silyl nitronates catalysed by B(C6F5)3 †. Chemical Science 15(7) (10.1039/d3sc05672d)
• Khan, M. N., van Ingen, Y., Boruah, T., McLauchlan, A., Wirth, T. and Melen, R. L. 2023. Advances in CO2 activation by frustrated Lewis pairs: from stoichiometric to catalytic reactions. Chemical Science 14(47), pp. 13661-13695. (10.1039/d3sc03907b)
• Ali, R., Patra, T. and Wirth, T. 2023. Alkene reactions with superoxide radical anions in flow electrochemistry. Faraday Discussions 247, pp. 297-301. (10.1039/D3FD00050H)
• Avanthay, M. et al. 2023. New strategies in organic electrosynthesis: General discussion. Faraday Discussions 247, pp. 125-131. (10.1039/D3FD90039H)
• Alkayal, A. et al. 2023. Flow cells and reactor design: General discussion. Faraday Discussions 247, pp. 333-341. (10.1039/D3FD90042H)
• Gutiérrez López, M. ?., Ali, R., Tan, M., Sakai, N., Wirth, T. and Matile, S. 2023. Electric field–assisted anion-π catalysis on carbon nanotubes in electrochemical microfluidic devices. Science Advances 9(41), article number: eadj5502. (10.1126/sciadv.adj5502)
• Boruah, T., Melen, R. L. and Wirth, T. 2023. Isodesmic metathesis chemistry: A novel way to recycle P(V). Chem Catalysis 3(8), article number: 100731. (10.1016/j.checat.2023.100731)
• Winterson, B., Bhattacherjee, D. and Wirth, T. 2023. Hypervalent halogen compounds in electrochemical reactions: advantages and prospects. Advanced Synthesis & Catalysis 365(16), pp. 2676-2689. (10.1002/adsc.202300412)
• Alkahtani, R. and Wirth, T. 2023. Synthesis of Chiral Iodoaniline-Lactate Based Catalysts for the α-Functionalization of Ketones. ACS Organic & Inorganic Au 3(4), pp. 209-216. (10.1021/acsorginorgau.3c00012)
• Ali, R., Babaahmadi, R., Didsbury, M., Stephens, R., Melen, R. L. and Wirth, T. 2023. Flow electrochemistry for the N‐Nitrosation of secondary amines. Chemistry - A European Journal 29(32), article number: e202300957. (10.1002/chem.202300957)
• Wirth, T. 2023. Hypervalent iodine in electrochemical reactions: advantages and prospects. SIS Letters(24)
• Alotaibi, N. et al. 2023. B(3,4,5-F3H2C6)3 Lewis acid-catalysed C3-allylation of indoles. Dalton Transactions 52(16) (10.1039/d3dt00745f)
• Spils, J., Wirth, T. and Nachtsheim, B. J. 2023. Two-step continuous-flow synthesis of 6-membered cyclic iodonium salts via anodic oxidation. Beilstein Journal of Organic Chemistry 19, pp. 27-32. (10.3762/bjoc.19.2)
• Patra, T. and Wirth, T. 2022. Oxidative cleavage of alkenes by photosensitized nitroarenes. Angewandte Chemie International Edition 61(47), article number: e202213772. (10.1002/anie.202213772)
• Singh, F. V., Shetgaonkar, S. E., Krishnan, M. and Wirth, T. 2022. Progress in organocatalysis with hypervalent iodine catalysts. Chemical Society Reviews 51(18), pp. 8102-8139. (10.1039/D2CS00206J)
• Khan, N., Itaya, K. and Wirth, T. 2022. Chiral iodotriptycenes: synthesis and catalytic applications. ChemistryOpen 11(8), article number: e202200158. (10.1002/open.202200158)
• Khan, N., Itaya, K. and Wirth, T. 2022. Chiral iodotriptycenes: Synthesis and catalytic applications. ChemistryOpen 11(7), article number: e202200145. (10.1002/open.202200145)
• Hareram, M. D. et al. 2022. Electrochemical deconstructive functionalization of cycloalkanols via alkoxy radicals enabled by proton-coupled Electron transfer. Organic Letters 24(21), pp. 3890-3895. (10.1021/acs.orglett.2c01552)
• Kaehler, T. et al. 2022. Borane promoted aryl transfer reaction for the synthesis of α-aryl functionalised β-hydroxy and β-keto esters. Organic and Biomolecular Chemistry 20(21), pp. 4298-4302. (10.1039/D2OB00643J)
• Xiong, Z., Weidlich, F., Sanchez, C. and Wirth, T. 2022. Biomimetic total synthesis of (−)-galanthamine via intramolecular anodic aryl–phenol coupling. Organic and Biomolecular Chemistry 20(20), pp. 4123-4127. (10.1039/D2OB00669C)
• Soldatova, N. S. et al. 2022. Zwitterionic iodonium species afford halogen bond-based porous organic frameworks. Chemical Science 13(19), pp. 5650-5658. (10.1039/D2SC00892K)
• Zhang, H. and Wirth, T. 2022. Oxidation of BINOLs by hypervalent iodine reagents: facile synthesis of xanthenes and lactones. Chemistry - A European Journal 28(21) (10.1002/chem.202200181)
• Wirth, T., Patra, T. and Winterson, B. 2022. Hypervalent bromine(III) compounds: synthesis, applications, prospects. Synthesis: Journal of Synthetic Organic Chemistry 54(5), pp. 1261-1271. (10.1055/a-1675-8404)
• Zhang, H., Cormanich, R. A. and Wirth, T. 2022. Chiral ligands in hypervalent iodine compounds: synthesis and structures of binaphthyl-based λ3-iodanes. Chemistry - A European Journal 28(5), article number: e202103623. (10.1002/chem.202103623)
• Amri, N. and Wirth, T. 2021. Flow electrosynthesis of sulfoxides, sulfones, and sulfoximines without supporting electrolytes. Journal of Organic Chemistry 86(22), pp. 15961-15972. (10.1021/acs.joc.1c00860)
• Amri, N. and Wirth, T. 2021. Recent advances in the electrochemical synthesis of organosulfur compounds. Chemical Record 21(9), pp. 2526-2537. (10.1002/tcr.202100064)
• Wirth, T. 2021. Iodine(III) mediators in electrochemical batch and flow reactions. Current Opinion in Electrochemistry 28, article number: 100701. (10.1016/j.coelec.2021.100701)
• Seitz, J. and Wirth, T. 2021. Electrochemical bromofunctionalization of alkenes in a flow reactor. Organic and Biomolecular Chemistry 19(31), pp. 6892-6896. (10.1039/D1OB01302E)
• Winterson, B., Rennigholtz, T. and Wirth, T. 2021. Flow electrochemistry: a safe tool for fluorine chemistry. Chemical Science 12(26), pp. 9053-9059. (10.1039/D1SC02123K)
• Dasgupta, A., Thiehoff, C., Newman, P. D., Wirth, T. and Melen, R. L. 2021. Reactions promoted by hypervalent iodine reagents and boron Lewis acids. Organic and Biomolecular Chemistry 19(22), pp. 4852-4865. (10.1039/D1OB00740H)
• Khan, M. N. and Wirth, T. 2021. Chiral Triptycenes: concepts, progress and prospects. Chemistry - A European Journal 27(24), pp. 7059-7068. (10.1002/chem.202005317)
• Alharbi, H., Elsherbini, M., Qurban, J. and Wirth, T. 2021. C−N axial chiral hypervalent iodine reagents: catalytic stereoselective α‐oxytosylation of ketones. Chemistry - A European Journal 27(13), pp. 4317-4321. (10.1002/chem.202005253)
• Yamamoto Raynbird, M., Khokhar, S., Neef, D., Evans, G. and Wirth, T. 2021. Synthesis of ajoene analogues by novel synthetic strategies. Chemistry - A European Journal 27(9), pp. 3008-3012. (10.1002/chem.202005023)
• Wirth, T. and Zhang, H. 2021. Recent advances in asymmetric functionalization of olefins induced by chiral hypervalent iodine reagents. Chinese Journal of Organic Chemistry 41(1), pp. 65-70. (10.6023/cjoc202006013)
• Elsherbini, M., Osi, A., Alharbi, H., Karam, F. and Wirth, T. 2021. Sulfur-based chiral iodoarenes: an underexplored class of chiral hypervalent iodine reagents. Synthesis: Journal of Synthetic Organic Chemistry 55, pp. 307-314. (10.1055/a-1508-9593)
• Singh, F. V. and Wirth, T. 2021. Hypervalent iodine chemistry and light: photochemical reactions involving hypervalent iodine Chemistry. ARKIVOC 2021(7), pp. 12-47. (10.24820/ark.5550190.p011.483)
• Wirth, T. and Amri, N. 2020. Accelerating electrochemical synthesis through automated flow: efficient synthesis of chalcogenophosphites. SYNLETT 31(19), pp. 1894-1898. (10.1055/s-0040-1707141)
• Hardwick, T., Cicala, R., Wirth, T. and Ahmed, N. 2020. Memory of chirality in a room temperature flow electrochemical reactor. Scientific Reports 10(1), article number: 16627. (10.1038/s41598-020-73957-6)
• Huynh, F., Tailby, M., Finniear, A., Stephens, K., Allemann, R. K. and Wirth, T. 2020. Accelerating biphasic biocatalysis through new process windows. Angewandte Chemie International Edition 59(38), pp. 16490-16495. (10.1002/anie.202005183)
• Elsherbini, M., Huynh, F., Dunbabin, A., Allemann, R. and Wirth, T. 2020. Selective hydroboration - oxidation of terminal alkenes under flow conditions. Chemistry - A European Journal 26(50), pp. 11423-11425. (10.1002/chem.202001650)
• Wirth, T. and Hokamp, T. 2020. Hypervalent iodine(III)‐catalysed enantioselective α‐acetoxylation of ketones. Chemistry - A European Journal 26(46), pp. 10417-10421. (10.1002/chem.202000927)
• Raynbird, M. Y., Silva, F., Smallman, H., Khokhar, S. S., Neef, D., Evans, G. J. S. and Wirth, T. 2020. Short total synthesis of ajoene, (E ,Z )‐4,5,9‐Trithiadodeca‐1,6,11‐triene 9‐oxide, in batch and (E ,Z )‐4,5,9‐Trithiadodeca‐1,7,11‐triene in continuous flow. Chemistry - A European Journal 26(38), pp. 8363-8367. (10.1002/chem.202001598)
• Valikhani, D., Srivastava, P. L., Allemann, R. K. and Wirth, T. 2020. Immobilised enzymes for sesquiterpene synthesis in batch and flow systems. ChemCatChem 12(8), pp. 2194-22197. (10.1002/cctc.201902135)
• Gazis, T. et al. 2020. 1,3-Carboboration of iodonium ylides. Chemical Communications 56, pp. 3345-3348. (10.1039/C9CC08749D)
• Amri, N. and Wirth, T. 2020. Automated electrochemical selenenylations. Synthesis 52(12), pp. 1751-1761. (10.1055/s-0039-1690868)
• Santi, M., Seitz, J., Cicala, R., Hardwick, T., Ahmed, N. and Wirth, T. 2019. Memory of chirality in flow electrochemistry: fast optimisation with DoE and online 2D-HPLC. Chemistry - A European Journal 25(71), pp. 16230-16235. (10.1002/chem.201904711)
• Elsherbini, M. and Wirth, T. 2019. Electroorganic synthesis under flow conditions. Accounts of Chemical Research 52(12), pp. 3287-3296. (10.1021/acs.accounts.9b00497)
• Allen, B. D. W., Mishra, D., Seastram, A. C., McBride, T., Wirth, T., Browne, D. L. and Morrill, L. C. 2019. Manganese-catalyzed electrochemical deconstructive chlorination of cycloalkanols via alkoxy radicals. Organic Letters 21(22), pp. 9241-9246. (10.1021/acs.orglett.9b03652)
• Elsherbini, M., Allemann, R. K. and Wirth, T. 2019. 'Dark' singlet oxygen made easy. Chemistry - A European Journal 25(54), pp. 12486-12490. (10.1002/chem.201903505)
• Gazis, T. A., Dasgupta, A., Hill, M. S., Rawson, J. M., Wirth, T. and Melen, R. L. 2019. Reactions of hydrazones and hydrazides with Lewis acidic boranes. Dalton Transactions(33), pp. 12391-12395. (10.1039/C9DT01359H)
• Elsherbini, M., Winterson, B., Alharbi, H., Folgueiras Amador, A. A., Genot, C. and Wirth, T. 2019. Continuous electrochemical generator of hypervalent iodine reagents: synthetic applications in flow. Angewandte Chemie International Edition 58(29), pp. 9811-9815. (10.1002/anie.201904379)
• Qurban, J., Elsherbini, M., Alharbi, H. and Wirth, T. 2019. Synthesis, characterisation, and reactivity of novel pseudocyclic hypervalent iodine reagents with heteroaryl carbonyl substituents. Chemical Communications 55, pp. 7998-8000. (10.1039/C9CC03905H)
• Yusubov, M. S. et al. 2019. 2-Iodoxybenzoic acid ditriflate: the most powerful hypervalent iodine(v) oxidant. Chemical Communications 55, pp. 7760-7763. (10.1039/C9CC04203B)
• Hokamp, T. and Wirth, T. 2019. Structurally defined α-Tetralol-Based chiral hypervalent iodine reagents. Journal of Organic Chemistry 84(13), pp. 8674-8682. (10.1021/acs.joc.9b01315)
• Santi, M., Ould, D. M. C., Wenz, J., Soltani, Y., Melen, R. L. and Wirth, T. 2019. Metal-free tandem rearrangement/lactonization: Access to 3,3-disubstituted benzofuran-2-(3H)-ones. Angewandte Chemie International Edition 58(23), pp. 7861-7865. (10.1002/anie.201902985)
• Wirth, T. and Knight, D. 2019. Morpholin-2-one derivatives via intramolecular acid-catalyzed hydroamination. SYNTHESIS 51(7), pp. 1643-1648. (10.1055/s-0037-1610674)
• Amri, N., Skilton, R., Guthrie, D. and Wirth, T. 2019. Efficient flow electrochemical alkoxylation of N-formylpyrrolidine. SYNLETT 30(10), pp. 1183-1186. (10.1055/s-0037-1611774)
• Soldatova, N. S., Postnikov, P. S., Yusubov, M. S. and Wirth, T. 2019. Flow synthesis of iodonium trifluoroacetates through direct oxidation of iodoarenes by Oxone®. European Journal of Organic Chemistry 2019(10), pp. 2081-2088. (10.1002/ejoc.201900220)
• Singh, F. V. and Wirth, T. 2019. Selenium reagents as catalysts. Catalysis Science & Technology 9(5), pp. 1073-1091. (10.1039/C8CY02274G)
• Islam, M., Kariuki, B. M., Shafiq, Z., Wirth, T. and Ahmed, N. 2018. Efficient electrosynthesis of thiazolidin-2-imines via oxysulfurization of thiourea-tethered terminal alkenes using the flow microreactor. European Journal of Organic Chemistry (10.1002/ejoc.201801688)
• Wirth, T., Gao, W., Xiong, Z. and Pirhaghani, S. 2018. Enantioselective electrochemical lactonization using chiral iodoarenes as mediators. Synthesis (Stuttgart) (10.1055/s-0037-1610373)
• Silva, F., Khokhar, S. S., Williams, D. M., Saunders, R., Evans, G. J. S., Graz, M. and Wirth, T. 2018. Short total synthesis of ajoene. Angewandte Chemie International Edition 57(38), pp. 12290-12293. (10.1002/anie.201808605)
• Elsherbini, M. and Wirth, T. 2018. Hypervalent iodine reagents by anodic oxidation: a powerful green synthesis. Chemistry - a European Journal 24(51), pp. 13399-13407. (10.1002/chem.201801232)
• Mironova, I. A. et al. 2018. Preparation and X-ray structure of 2-iodoxybenzenesulfonic acid (IBS) - a powerful hypervalent iodine(V) oxidant. Beilstein Journal of Organic Chemistry 14, pp. 1854-1858. (10.3762/bjoc.14.159)
• Hokamp, T., Mollari, L., Wilkins, L. C., Melen, R. L. and Wirth, T. 2018. Alternative strategies with iodine: fast access to previously inaccessible iodine(III) compounds. Angewandte Chemie International Edition 57(27), pp. 8306-8309. (10.1002/anie.201804642)
• Elsherbini, M. and Wirth, T. 2018. Mechanochemical synthesis of N-tert-butanesulfinyl imines under metal-free conditions. Tetrahedron 74(25), pp. 3101-3106. (10.1016/j.tet.2017.11.028)
• Silva, F. et al. 2018. Selective oxidation of sulfides in flow chemistry. European Journal of Organic Chemistry 2018(18), pp. 2134-2137. (10.1002/ejoc.201800339)
• Soldatova, N., Postnikov, P., Kukurina, O., Zhdankin, V. V., Yoshimura, A., Wirth, T. and Yusubov, M. S. 2018. One-pot synthesis of diaryliodonium salts from arenes and aryl iodides with Oxone-sulfuric acid. Beilstein Journal of Organic Chemistry 14, pp. 849-855. (10.3762/bjoc.14.70)
• Yusubov, M. et al. 2018. Reactions of 1-arylbenziodoxolones with azide anion: Experimental and computational study of substituent effects. European Journal of Organic Chemistry 2018(5), pp. 640-647. (10.1002/ejoc.201701595)
• Folgueiras-Amador, A. A., Qian, X., Xu, H. and Wirth, T. 2018. Catalyst- and supporting electrolyte-free electrosynthesis of benzothiazoles and thiazolopyridines in continuousf flow. Chemistry - A European Journal 24(2), pp. 487-491. (10.1002/chem.201705016)
• Wirth, T., Hokamp, T., Storm, A. and Yusubov, M. 2018. Iodine monoacetate for efficient oxyiodinations of alkenes and alkynes. Synlett 29(4), pp. 415-418. (10.1055/s-0036-1589119)
• Wirth, T. 2017. Integration of flow chemistry in multistep syntheses. European Journal of Organic Chemistry 2017(44), pp. 6464. (10.1002/ejoc.201701543)
• Folgueiras-Amador, A. A., Philipps, K., Guilbaud, S., Poelakker, J. and Wirth, T. 2017. An easy-to-machine electrochemical flow microreactor: efficient synthesis of isoindolinone and flow functionalization. Angewandte Chemie International Edition 56(48), pp. 15446-15450. (10.1002/anie.201709717)
• Wirth, T. 2017. Thomas Wirth. European Journal of Organic Chemistry 2017(44), pp. 6465-6464. (10.1002/ejoc.201701545)
• Wirth, T. 2017. Organic synthesis in flow for medicinal chemistry. Bioorganic & Medicinal Chemistry 25(23), pp. 6179. (10.1016/j.bmc.2017.11.013)
• Aldmairi, A. H., Knight, D. and Wirth, T. 2017. Acid-catalyzed tandem process for the one-pot synthesis of oxazolidines. Synlett 28(20), pp. 2976-2978. (10.1055/s-0036-1591513)
• Qurban, J., Elsherbini, M. and Wirth, T. 2017. Electron-deficient chiral lactic acid-based hypervalent iodine reagents. Journal of Organic Chemistry 82(22), pp. 11872-11876. (10.1021/acs.joc.7b01571)
• Folgueiras-Amador, A. and Wirth, T. 2017. Perspectives in flow electrochemistry. Journal of Flow Chemistry 7(3-4), pp. 94-95. (10.1556/1846.2017.00020)
• Santi, M., Müller, S. T. R., Folgueiras-Amador, A., Uttry, A., Hellier, P. and Wirth, T. 2017. Enantioselective synthesis of trans-2,3-Dihydro-1H-indoles through C-H Insertion of a-Diazocarbonyl compounds. European Journal of Organic Chemistry 2017(14), pp. 1889-1893. (10.1002/ejoc.201700412)
• Tang, X., Demiray, M., Wirth, T. and Allemann, R. K. 2017. Concise synthesis of artemisinin from a farnesyl diphosphate analogue. Bioorganic & Medicinal Chemistry 26(7), pp. 1314-1319. (10.1016/j.bmc.2017.03.068)
• Demiray, M., Tang, X., Wirth, T., Faraldos, J. A. and Allemann, R. K. 2017. An efficient chemoenzymatic synthesis of dihydroartemisinic aldehyde. Angewandte Chemie International Edition 56(15), pp. 4347-4350. (10.1002/anie.201609557)
• Demiray, M., Tang, X., Wirth, T., Faraldos, J. A. and Allemann, R. K. 2017. Effiziente chemoenzymatische Synthese von dhydroartemisinaldehyd. Angewandte Chemie 129(15), pp. 4411-4415. (10.1002/ange.201609557)
• Wirth, T. 2017. Novel organic synthesis through ultrafast chemistry. Angewandte Chemie - International Edition 56(3), pp. 682-684. (10.1002/anie.201609595)
• Wirth, T. 2017. Neue organische synthesen durch ultraschnelle chemie. Angewandte Chemie 129(3), pp. 698-700. (10.1002/ange.201609595)
• Tang, X., Allemann, R. K. and Wirth, T. 2017. Optimising terpene synthesis with flow biocatalysis. European Journal of Organic Chemistry 2017(2), pp. 414-418. (10.1002/ejoc.201601388)
• Malmedy, F. and Wirth, T. 2017. Cyclization of malonate derivatives with iodine(III) reagents. European Journal of Organic Chemistry (10.1002/ejoc.201601587)
• Wirth, T. and Mizar, P. 2017. Iodoaminations of alkenes. Synthesis 49(5), pp. 981-986. (10.1055/s-0036-1588630)
• Soldatova, N., Postnikov, P., Kukurina, O., Zhdankin, V. V., Yoshimura, A., Wirth, T. and Yusubov, M. S. 2016. Facile one-pot synthesis of diaryliodonium salts from arenes and aryl iodides with oxone. ChemistryOpen (10.1002/open.201600129)
• Hutchings, M. and Wirth, T. 2016. Safe use of nitromethane for aldol reactions in flow. Journal of Flow Chemistry 6(3), pp. 202-205. (10.1556/1846.2016.00022)
• Malmedy, F. and Wirth, T. 2016. Stereoselective ketone rearrangements with hypervalent iodine reagents. Chemistry - a European Journal 22(45) (10.1002/chem.201603022)
• Malmedy, F. and Wirth, T. 2016. Frontispiece: stereoselective ketone rearrangements with hypervalent iodine reagents. Chemistry - a European Journal 22(45), pp. 16072-16077. (10.1002/chem.201684562)
• Wilkins, L. C., Gunther, B. A. R., Walther, M., Lawson, J. R., Wirth, T. and Melen, R. L. 2016. Contrasting frustrated Lewis pair reactivity with selenium- and boron-based Lewis acids. Angewandte Chemie International Edition 55(37), pp. 11292-11295. (10.1002/anie.201605239)
• Wilkins, L., Günther, B. A., Walther, M., Lawson, J., Wirth, T. and Melen, R. 2016. Gegensätzliche Reaktivität frustrierter Lewis-Paare mit Selen- und Bor-basierten Lewis-Säuren. Angewandte Chemie 128(37), pp. 11462-11465. (10.1002/ange.201605239)
• Müller, S. T. R., Hokamp, T., Ehrmann, S., Hellier, P. and Wirth, T. 2016. Ethyl lithiodiazoacetate: extremely unstable intermediate handled efficiently in flow. Chemistry: A European Journal 22(34), pp. 11940-11942. (10.1002/chem.201602133)
• Wirth, T. and Hutchings, M. 2016. A simple setup for transfer hydrogenations in flow chemistry. Synlett 27(12), pp. 1832-1835. (10.1055/s-0035-1561624)
• Brown, M., Kumar, R., Rehbein, J. and Wirth, T. 2016. Enantioselective oxidative rearrangements with chiral hypervalent iodine reagents. Chemistry - a European Journal 22(12), pp. 4030-4035. (10.1002/chem.201504844)
• Mueller, S. T. R., Murat, A., Hellier, P. and Wirth, T. 2016. Toward a large-scale approach to milnacipran analogues using diazo compounds in flow chemistry. Organic Process Research and Development 20(2), pp. 495-502. (10.1021/acs.oprd.5b00308)
• Mizar, P., Niebuhr, R., Hutchings, M., Farooq, U. and Wirth, T. 2016. Thioamination of alkenes with hypervalent iodine reagents. Chemistry - a European Journal 22(5), pp. 1614-1617. (10.1002/chem.201504636)
• Edwards, R., de Vries, W., Westwell, A. D., Daniels, S. and Wirth, T. 2015. Solid-supported iodonium salts for fluorinations. European Journal of Organic Chemistry 2015(31), pp. 6909-6916. (10.1002/ejoc.201500992)
• Muller, S. T. R., Murat, A., Hellier, P. and Wirth, T. 2015. Safe handling of diazo reagents through inline analytics and flow chemistry. Chimica Oggi 33(5), pp. 74-77.
• Wirth, T. 2015. Kleine Organoselenverbindungen: mehr als nur Mimetika der Glutathion-Peroxidase. Angewandte Chemie 127(35), pp. 10212-10214. (10.1002/ange.201505056)
• Wirth, T. 2015. Small organoselenium compounds: more than just glutathione peroxidase mimics. Angewandte Chemie - International Edition 54(35), pp. 10074-10076. (10.1002/anie.201505056)
• Baker, A., Graz, M., Saunders, R., Evans, G. J. S., Pitotti, I. and Wirth, T. 2015. Flow alkylation of thiols, phenols, and amines using a heterogenous base in a packed-bed reactor. Journal of Flow Chemistry 5(2), pp. 65. (10.1556/1846.2015.00009)
• Tancock, J. and Wirth, T. 2015. Selenium-mediated synthesis of tetrasubstituted naphthalenes through rearrangement. Molecules 20(6), pp. 10866-10872. (10.3390/molecules200610866)
• Kumar, R. and Wirth, T. 2015. Asymmetric synthesis with hypervalent iodine reagents. Topics in Current Chemistry, pp. 1-19. (10.1007/128_2015_639)
• Edwards, R. and Wirth, T. 2015. [18F]6-fluoro-3,4-dihydroxy-l-phenylalanine - recent modern syntheses for an elusive radiotracer. Journal of Labelled Compounds and Radiopharmaceuticals 58(5), pp. 183-187. (10.1002/jlcr.3285)
• Muller, S. T. R., Murat, A., Maillos, D., Lesimple, P., Hellier, P. and Wirth, T. 2015. Rapid generation and safe use of carbenes enabled by a novel flow protocol with in-line IR spectroscopy. Chemistry - A European Journal 21(19), pp. 7016-7020. (10.1002/chem.201500416)
• Müller, S. T. R. and Wirth, T. 2015. Diazo compounds in continuous-flow technology. Chemsuschem 8(2), pp. 245-250. (10.1002/cssc.201402874)
• Edwards, R., Westwell, A. D., Daniels, S. and Wirth, T. 2015. Convenient synthesis of diaryliodonium salts for the production of [18F]F-DOPA. European Journal of Organic Chemistry 2015(3), pp. 625-630. (10.1002/ejoc.201403378)
• Wirth, T., Brown, M., Delorme, M., Malmedy, F., Malmgren, J. and Olofsson, B. 2015. Synthesis of new chiral diaryliodonium salts. Synlett 26(11), pp. 1573-1577. (10.1055/s-0034-1380687)
• Attah Egu, S., Okoro, U. and Wirth, T. 2014. Synthesis of quinolinequinone derivatives and related carbocyclic compounds. ScienceOpen Research (10.14293/S2199-1006.1.SOR-CHEM.AALL9P.v1)
• Ambreen, N. and Wirth, T. 2014. High-temperature synthesis of amides from alcohols or aldehydes by using flow chemistry. European Journal of Organic Chemistry 2014(34), pp. 7590-7593. (10.1002/ejoc.201403280)
• Elsherbini, M. S., Hamama, W. S., Zoorob, H. H., Bhowmick, D., Mugesh, G. and Wirth, T. 2014. Synthesis and antioxidant activities of novel chiral ebselen analogues. Heteroatom Chemistry 25(5), pp. 320-325. (10.1002/hc.21164)
• Mizar, P., Burrelli, A., Gunther, E., Softje, M., Farooq, U. and Wirth, T. 2014. Organocatalytic stereoselective iodoamination of alkenes. Chemistry - a European Journal 20(41), pp. 13113-13116. (10.1002/chem.201404762)
• Mizar, P., Laverny, A., El-Sherbini, M., Farid, U., Brown, M., Malmedy, F. and Wirth, T. 2014. Enantioselective diamination with novel chiral hypervalent iodine catalysts. Chemistry - A European Journal 20(32), pp. 9910-9913. (10.1002/chem.201403891)
• Arai, K. and Wirth, T. 2014. Rapid electrochemical deprotection of the isonicotinyloxycarbonyl group from carbonates and thiocarbonates in a microfluidic reactor. Organic Process Research and Development, article number: 140708073813000. (10.1021/op500155f)
• Mizar, P. and Wirth, T. 2014. Flexible stereoselective functionalizations of ketones through umpolung with hypervalent iodine reagents. Angewandte Chemie International Edition 53(23), pp. 5993-5997. (10.1002/anie.201400405)
• Mizar, P. and Wirth, T. 2014. Flexible stereoselektive Funktionalisierung von Ketonen durch Umpolung mit hypervalenten Iodreagentien. Angewandte Chemie 126(23), pp. 6103-6107. (10.1002/ange.201400405)
• Muller, S. T. R., Smith, D., Hellier, P. and Wirth, T. 2014. Safe generation and direct use of diazoesters in flow chemistry. Synlett 25(6), pp. 871-875. (10.1055/s-0033-1340835)
• Arai, K., Watts, K. and Wirth, T. 2014. Difluoro- and trifluoromethylation of electron-deficient alkenes in an electrochemical microreactor. ChemistryOpen 3(1), pp. 23-28. (10.1002/open.201300039)
• Watts, K., Baker, A. R. and Wirth, T. 2014. Electrochemical synthesis in microreactors. Journal of Flow Chemistry 4(1), pp. 2-11. (10.1556/JFC-D-13-00030)
• Singh, F. V. and Wirth, T. 2014. 7.29 oxidative functionalization with hypervalent halides. Reference Module in Chemistry, Molecular Sciences and Chemical Engineering 7, pp. 880-933. (10.1016/B978-0-08-097742-3.00735-7)
• Singh, F. V. and Wirth, T. 2014. Hypervalent iodine-catalyzed oxidative functionalizations including stereoselective reactions. Chemistry - An Asian Journal 9(4), pp. 950-971. (10.1002/asia.201301582)
• Baker, A. R., Graz, M., Saunders, R., Evans, G. J. S., Kaul, S. and Wirth, T. 2013. Flow synthesis of symmetrical di- and trisulfides using phase-transfer catalysis. Journal of Flow Chemistry 3(4), pp. 118-121. (10.1556/JFC-D-13-00013)
• Cascón, O., Richter, G., Allemann, R. K. and Wirth, T. 2013. Efficient terpene synthase catalysis by extraction in flow. ChemPlusChem 78(11), pp. 1334-1337. (10.1002/cplu.201300303)
• Singh, F. V. and Wirth, T. 2013. Oxidative rearrangements with hypervalent iodine reagents. Synthesis (Stuttgart) 45(18), pp. 2499-2511. (10.1055/s-0033-1339679)
• Farid, U., Malmedy, F., Claveau, R., Albers, L. and Wirth, T. 2013. Stereoselective rearrangements with chiral hypervalent iodine reagents. Angewandte Chemie - International Edition 52(27), pp. 7018-7022. (10.1002/anie.201302358)
• König, B., Kreitmeier, P., Hilgers, P. and Wirth, T. 2013. Flow chemistry in undergraduate organic chemistry education. Journal of Chemical Education 90(7), pp. 934-936. (10.1021/ed3006083)
• Brown, M., Farid, U. and Wirth, T. 2013. Hypervalent iodine reagents as powerful electrophiles. Synlett 24(4), pp. 424-431. (10.1055/s-0032-1318103)
• Farid, U., Malmedy, F., Claveau, R., Albers, L. and Wirth, T. 2013. Stereoselektive Umlagerungen mit chiralen hypervalenten Iodreagentien. Angewandte Chemie 125(27), pp. 7156-7160. (10.1002/ange.201302358)
• Ambreen, N., Kumar, R. and Wirth, T. 2013. Hypervalent iodine/TEMPO-mediated oxidation in flow systems: a fast and efficient protocol for alcohol oxidation. Beilstein Journal of Organic Chemistry 9, pp. 1437-1442. (10.3762/bjoc.9.162)
• Singh, F. V., Rehbein, J. and Wirth, T. 2012. Facile oxidative rearrangements using hypervalent iodine reagents. ChemistryOpen 1(6), pp. 245-250. (10.1002/open.201200037)
• Gabriele, E., Singh, F. V., Freudendahl, D. M. and Wirth, T. 2012. Selenenylations of alkenes with styrene nucleophiles. Tetrahedron 68(51), pp. 10573-10576. (10.1016/j.tet.2012.08.034)
• Santi, C., Di Lorenzo, R., Tidei, C., Bagnoli, L. and Wirth, T. 2012. Stereoselective selenium catalyzed dihydroxylation and hydroxymethoxylation of alkenes. Tetrahedron 68(51), pp. 10530-10535. (10.1016/j.tet.2012.08.078)
• Farid, U. and Wirth, T. 2012. 5,6,7,8-Tetrafluoro-1-hydroxy-1-oxobenziodoxol-3(1H)one (Tetrafluoro-IBX). e-EROS: Encyclopedia of Reagents for Organic Synthesis, article number: rn01489. (10.1002/047084289X.rn01489)
• Wirth, T. 2012. Flow chemistry: enabling technology in drug discovery and process research [Editorial]. ChemSusChem 5(2), pp. 215-216. (10.1002/cssc.201200061)
• Singh, F. V. and Wirth, T. 2012. Hypervalent iodine mediated oxidative cyclization of o-hydroxystilbenes into benzo- and naphthofurans. Synthesis (Stuttgart) 44(8), pp. 1171-1177. (10.1055/s-0031-1290588)
• Martínez-Máñez, R. and Wirth, T. 2012. Opening up the world of chemistry [Editorial]. ChemistryOpen 1(1), pp. 4. (10.1002/open.201100009)
• Audiger, L. E., Watts, K., Elmore, S. C., Robinson, R. I. and Wirth, T. 2012. Ritter reactions in flow. ChemSusChem 5(2), pp. 257-260. (10.1002/cssc.201100372)
• Zhao, L., Li, J., Li, Y., Liu, J., Wirth, T. and Li, Z. 2012. Selenium-containing naphthalimides as anticancer agents: Design, synthesis and bioactivity. Bioorganic and Medicinal Chemistry 20(8), pp. 2558-2563. (10.1016/j.bmc.2012.02.049)
• Farid, U. and Wirth, T. 2012. Highly stereoselective metal-free oxyaminations using chiral hypervalent iodine reagents. Angewandte Chemie. International Edition 51(14), pp. 3462-3465. (10.1002/anie.201107703)
• Farid, U. and Wirth, T. 2012. Innenrücktitelbild: stereoselektive metallfreie oxyaminierungen mit chiralen hypervalenten iodreagentien (Angew. Chem. 14/2012). Angewandte Chemie 124(14), pp. 3549. (10.1002/ange.201201230)
• Farid, U. and Wirth, T. 2012. Inside back cover: highly stereoselective metal-free oxyaminations using chiral hypervalent iodine reagents (Angew. Chem. Int. Ed. 14/2012). Angewandte Chemie - International Edition 51(14), pp. 3491. (10.1002/anie.201201230)
• Zhao, L., Li, Z. and Wirth, T. 2011. Asymmetric Methoxyselenenylations with Chiral Selenium Electrophiles. European Journal of Organic Chemistry 2011(35), pp. 7080-7082. (10.1002/ejoc.201101373)
• Watts, K., Gattrell, W. and Wirth, T. 2011. A practical microreactor for electrochemistry in flow. Beilstein Journal of Organic Chemistry 7, pp. 1108-1114. (10.3762/bjoc.7.127)
• Rasheed, M. and Wirth, T. 2011. Fast optimisation of a Diels-Alder reaction in a flow microreactor by in-line HPLC analysis. Chimica Oggi - Chemistry Today 29(3), pp. 53-55.
• Wirth, T. and Zanda, M. 2011. SYNTHESIS/SYNLETT Advisory Board Focus: Professor Thomas Wirth (Cardiff University, UK) [Interview]. Synthesis -Stuttgart-(5), pp. A26-A26. (10.1055/s-0030-1259586)
• Ahmed-Omer, B., Barrow, D. A. and Wirth, T. 2011. Multistep reactions using microreactor chemistry. Arkivoc Online Journal of Organic Chemistry(4), pp. 26-36.
• Zhao, L., Li, Z. and Wirth, T. 2011. Preparation of Novel Chiral Non-Racemic Diselenides and Applications in Asymmetric Synthesis. European Journal of Organic Chemistry(1), pp. 176-182. (10.1002/ejoc.201001272)
• Rasheed, M. and Wirth, T. 2011. Intelligent Microflow: Development of Self-Optimizing Reaction Systems. Angewandte Chemie - International Edition 50(2), pp. 357-358. (10.1002/anie.201006107)
• Wirth, T. 2011. Professor Siegfried Blechert: A Tribute. Arkivoc Online Journal of Organic Chemistry(4), pp. 1-5.
• Singh, F. V. and Wirth, T. 2011. Selenium-catalyzed regioselective cyclization of unsaturated carboxylic acids using hypervalent iodine oxidants. Organic Letters 13(24), pp. 6504-6507. (10.1021/ol202800k)
• Brandt, J. C., Elmore, S. C., Robinson, R. I. and Wirth, T. 2010. Safe and Efficient Ritter Reactions in Flow. Synlett(20), pp. 3099-3103. (10.1055/s-0030-1259075)
• Luk, Y., Allender, C. J. and Wirth, T. 2010. Molecular imprinted polymers binding low functionality templates. Tetrahedron Letters 51(45), pp. 5883-5885. (10.1016/j.tetlet.2010.08.108)
• Khan, Z. A., Iwaoka, M. and Wirth, T. 2010. Novel cyclization cascades to functionalized indanes and tetrahydronaphthalenes. Tetrahedron 66(33), pp. 6639-6646. (10.1016/j.tet.2010.03.062)
• Zhao, L. W., Li, Z. and Wirth, T. 2010. Triptycene Derivatives: Synthesis and Applications. Chemistry Letters 39(7), pp. 658-667.
• Freudendahl, D. M., Iwaoka, M. and Wirth, T. 2010. Synthesis of New Sulfoxide-Containing Diselenides and Unexpected Cyclization Reactions to 2,3-Dihydro-1,4-benzoselenothiine 1-Oxides. European Journal of Organic Chemistry(20), pp. 3934-3944. (10.1002/ejoc.201000514)
• Altermann, S., Schafer, S. and Wirth, T. 2010. New chiral hypervalent iodine(V) compounds as stoichiometric oxidants. Tetrahedron 66(31), pp. 5902-5907. (10.1016/j.tet.2010.05.079)
• Quideau, S. and Wirth, T. 2010. Hypervalent iodine chemistry-recent advances and applications [Preface]. Tetrahedron 66(31), pp. 5737-5738. (10.1016/j.tet.2010.06.026)
• Shahzad, S. A., Venin, C. and Wirth, T. 2010. Diselenide- and Disulfide-Mediated Synthesis of Isocoumarins. European Journal of Organic Chemistry(18), pp. 3465-3472. (10.1002/ejoc.201000308)
• Farooq, U., Schäfer, S., Shah, A., Freudendahl, D. M. and Wirth, T. 2010. Synthesis of new enantiomerically pure organoiodine catalysts and their application in the alpha-functionalization of ketones. Synthesis -Stuttgart-(6), pp. 1023-1029. (10.1055/s-0029-1218640)
• Shahzad, S. A., Vivant, C. and Wirth, T. 2010. Selenium-Mediated Synthesis of Biaryls through Rearrangement. Organic Letters 12(6), pp. 1364-1367. (10.1021/ol100274e)
• Schäfer, S. and Wirth, T. 2010. A versatile and highly reactive polyfluorinated hypervalent iodine(III) compound. Angewandte Chemie. International Edition 49(15), pp. 2786-2789. (10.1002/anie.200907134)
• Ahmed-Omer, B., Barrow, D. A. and Wirth, T. 2009. Heck reactions using segmented flow conditions. Tetrahedron Letters 50(26), pp. 3352-3355. (10.1016/j.tetlet.2009.02.133)
• Brandt, J. C. and Wirth, T. 2009. Controlling hazardous chemicals in microreactors: Synthesis with iodine azide. Beilstein Journal of Organic Chemistry 5(30) (10.3762/bjoc.5.30)
• Freudendahl, D. M., Shahzad, S. A. and Wirth, T. 2009. Recent Advances in Organoselenium Chemistry. European Journal of Organic Chemistry(11), pp. 1649-1664. (10.1002/ejoc.200801171)
• Khan, Z. A. and Wirth, T. 2009. Synthesis of Indene Derivatives via Electrophilic Cyclization. Organic Letters 11(1), pp. 229-231. (10.1021/ol8024956)
• Shah, A. et al. 2009. Iodoxolone-Based Hypervalent Iodine Reagents. Organic Letters 11(16), pp. 3578-3581. (10.1021/ol9014688)
• Shahzad, S. A. and Wirth, T. 2009. Fast synthesis of benzofluorenes by selenium-mediated carbocyclizations. Angewandte Chemie. International Edition 48(14), pp. 2588-2591. (10.1002/anie.200806148)
• Farooq, U., Shah, A. and Wirth, T. 2009. Hypervalent Bromine Compounds: Smaller, More Reactive Analogues of Hypervalent Iodine Compounds. Angewandte Chemie - International Edition 48(6), pp. 1018-1020. (10.1002/anie.200805027)
• Freudendahl, D. M., Santoro, S., Shahzad, S. A., Santi, C. and Wirth, T. 2009. Green Chemistry with Selenium Reagents: Development of Efficient Catalytic Reactions. Angewandte Chemie - International Edition 48(45), pp. 8409-8411. (10.1002/anie.200903893)
• Uehlin, L. and Wirth, T. 2009. Synthesis of Chiral Acetals by Asymmetric Selenenylations. Phosphorus Sulfur and Silicon and the Related Elements 184(6), pp. 1374-1385. (10.1080/10426500902930167)
• Altermann, S. M. et al. 2008. Catalytic Enantioselective alpha-Oxysulfonylation of Ketones Mediated by Iodoarenes. European Journal of Organic Chemistry(31), pp. 5315-5328. (10.1002/ejoc.200800741)
• Browne, D. M., Niyomura, O. and Wirth, T. 2008. Catalytic addition-elimination reactions towards butenolides. Phosphorus Sulfur and Silicon and the Related Elements 183(4), pp. 1026-1035. (10.1080/10426500801901053)
• Ahmed-Omer, B., Barrow, D. A. and Wirth, T. 2008. Effect of segmented fluid flow, sonication and phase transfer catalysis on biphasic reactions in capillary microreactors. Chemical Engineering Journal 135(S1), pp. S280-S283. (10.1016/j.cej.2007.07.017)
• Richardson, R. D. and Wirth, T. 2008. Tetraazafulvalene: "Organisches" Natrium. Chemie in unserer Zeit 42(3), pp. 190-191. (10.1002/ciuz.200890032)
• Browne, D. M., Niyomura, O. and Wirth, T. 2007. Catalytic use of selenium electrophiles in cyclizations. Organic Letters 9(16), pp. 3169-3171. (10.1021/ol071223y)
• Richardson, R. D., Zayed, J. M., Altermann, S., Smith, D. and Wirth, T. 2007. Tetrafluoro-IBA and -IBX: Hypervalent Iodine Reagents. Angewandte Chemie - International Edition 46(34), pp. 6529-6532. (10.1002/anie.200702313)
• Simmons, S. J., French, A. N., Richardson, R. D. and Wirth, T. 2007. Attempted aziridinations and sulfonilimations using simple iron catalysts and hypervalent iodine reagents. Abstracts of Papers of the American Chemical Society 233, pp. 253-253.
• Paradine, S. M., French, A. N., Page, T. K., Richardson, R. D. and Wirth, T. 2007. Catalytic enantioselective alpha-oxytosylation of propiophenone using chiral hypervalent iodine reagents. Abstracts of Papers of the American Chemical Society 233, pp. 211-211.
• Burgler, F. W., Fragale, G. and Wirth, T. 2007. Stereoselective addition reactions with chalcogen electrophiles. Arkivoc(x), pp. 21-28.
• Ahmed-Omer, B., Brandt, J. C. and Wirth, T. 2007. Advanced organic synthesis using microreactor technology. Organic & Biomolecular Chemistry 5(5), pp. 733-740. (10.1039/B615072A)
• Richardson, R. D., Desaize, M. and Wirth, T. 2007. Hypervalent iodine-mediated aziridination of alkenes: Mechanistic insights and requirements for catalysis. Chemistry - A European Journal 13(23), pp. 6745-6754. (10.1002/chem.200700306)
• Ahmed, B., Barrow, D. A. and Wirth, T. 2006. Enhancement of reaction rates by segmented fluid flow in capillary scale reactors. Advanced Synthesis & Catalysis 348(9), pp. 1043-1048. (10.1002/adsc.200505480)
• Niyomura, O., Cox, M. and Wirth, T. 2006. Electrochemical generation and catalytic use of selenium electrophiles. Synlett(2), pp. 251-254. (10.1055/s-2005-923585)
• Haas, J., Bissmire, S. and Wirth, T. 2005. Iodine Monochloride-Amine Complexes: An Experimental and Computational Approach to New Chiral Electrophiles. Chemistry - A European Journal 11(19), pp. 5777-5785. (10.1002/chem.200500507)
• Yusubov, M. S. and Wirth, T. 2005. Solvent-free reactions with hypervalent iodine reagents. Organic Letters 7(3), pp. 519-521. (10.1021/ol047363e)
• Wirth, T. 2005. Hypervalent iodine chemistry in synthesis: Scope and new directions. Angewandte Chemie - International Edition 44(24), pp. 3656-3665. (10.1002/anie.200500115)
• French, A. N., Cole, J. and Wirth, T. 2004. Tetrahydrofuranylation of alcohols using hypervalent iodine reagents. Synlett(13), pp. 2291-2294. (10.1055/s-2004-832810)
• Khokhar, S. S. and Wirth, T. 2004. Nucleophile-selective selenocyclizations. European Journal of Organic Chemistry(22), pp. 4567-4581. (10.1002/ejoc.200400526)
• Khokhar, S. S. and Wirth, T. 2004. Selenocyclizations: control by coordination and by the counterion. Angewandte Chemie - International Edition 43(5), pp. 631-633. (10.1002/anie.200352884)
• Jauslin, M. L., Wirth, T., Meier, T. and Schoumacher, F. 2002. A cellular model for Friedreich Ataxia reveals small-molecule glutathione peroxidase mimetics as novel treatment strategy. Human Molecular Genetics 11(24), pp. 3055-3063. (10.1093/hmg/11.24.3055)
• Schoumacher, F., Jauslin, M. L., Wirth, T. and Meier, T. 2002. A cellular model for Friedrich ataxia and its application in drug discovery. Neuromuscular Disorders 12(7-8), pp. 774-774.
• Uehlin, L., Fragale, G. and Wirth, T. 2002. New and Efficient Chiral Selenium Electrophiles. Chemistry - A European Journal 8(5), pp. 1125-1133. (10.1002/1521-3765(20020301)8:5<1125::AID-CHEM1125>3.0.CO;2-I)
• Uehlin, L. and Wirth, T. 2001. Novel polymer-bound chiral selenium electrophiles. Organic Letters 3(18), pp. 2931-2933. (10.1021/ol0164435)
• Burpee, S. J., French, A. N., Haas, J. and Wirth, T. 2001. Progress in a computational investigation of conformers of chiral hypervalent iodine compounds. Abstracts of Papers of the American Chemical Society 221, pp. U170-U171.
• Uehlin, L. and Wirth, T. 2001. Chiral selenium electrophiles on solid-support. Chimia 55(1-2), pp. 65-67.
• Wirth, T. 2001. IBX - New reactions with an old reagent. Angewandte Chemie - International Edition 40(15), pp. 2812-2814. (10.1002/1521-3773(20010803)40:15<2812::AID-ANIE2812>3.0.CO;2-X)
• Uehlin, L. and Wirth, T. 2001. Mixed acetals as new precursors for selenium electrophiles. Phosphorus, Sulfur and Silicon and the Related Elements 171(1), pp. 189-194. (10.1080/10426500108046650)
• Spichty, M., Fragale, G. and Wirth, T. 2000. Theoretical investigations on the stereoselective selenenylation reaction of alkenes. Journal of the American Chemical Society 122(44), pp. 10914-10916. (10.1021/ja001602l)
• Wirth, T. 2000. Organoselenium chemistry in stereoselective reactions. Angewandte Chemie - International Edition 39(21), pp. 3740-3749. (10.1002/1521-3773(20001103)39:21<3740::AID-ANIE3740>3.0.CO;2-N)

Book sections

• Singh, F. and Wirth, T. 2024. Selected Diastereoselective Reactions: Hypervalent iodine chemistry. In: Cossy, J. ed. Comprehensive Chirality Volume 1: Chiral Pool and Diastereoselective Synthesis. Elsevier
• Rahman, M. T. and Wirth, T. 2024. Sicherer Umgang mit gefährlichen Chemikalien im Durchfluss. In: Sharma, U. K. and Van der Eycken, E. V. eds. Flow-Chemie für die Synthese von Heterocyclen. Cham: Springer, pp. 375–408., (10.1007/978-3-031-51912-3_8)
• Winterson, B. and Wirth, T. 2020. Electrochemistry in flow for drug discovery. In: Topics in Medicinal Chemistry., Vol. 38. Springer, pp. 121-172., (10.1007/7355_2021_115)
• Folgueiras Amador, A. and Wirth, T. 2019. Electrochemistry under flow conditions. In: Luis, S. V. and Garcia-Verdugo, E. eds. Flow Chemistry: Integrated Approaches for Practical Applications. Green Chemistry Series Royal Society of Chemistry, pp. 153-198., (10.1039/9781788016094-00153)
• Singh, F. V. and Wirth, T. 2019. 7. Selenium and tellurium electrophiles in organic synthesis. In: Laitinen, R. and Oilunkaniemi, R. eds. Selenium and Tellurium Reagents: In Chemistry and Materials Science. De Gruyter, pp. 243-300., (10.1515/9783110529340-007)
• Wirth, T. 2018. Organoselenium chemistry. In: Encyclopedia of Inorganic and Bioinorganic Chemistry. Wiley, (10.1002/9781119951438.eibc2727)
• Singh, F. V. and Wirth, T. 2018. Stereoselective reactions. In: PATAI's Chemistry of Functional Groups. John Wiley, (10.1002/9780470682531.pat0957)
• Wirth, T. and Singh, F. V. 2017. 2.2 Catalytic oxidations with hypervalent iodine. In: Muniz, K. ed. Science of Synthesis: Catalytic Oxidation in Organic Synthesis. Thieme, pp. 29-62.
• Wirth, T. 2017. 35.1.5.1.12 Synthesis of 1-Chloro-n-Heteroatom-Functionalized Alkanes (n ≥2) by Addition across C=C Bonds. In: Science of Synthesis Knowledge Updates 2017/1. Georg Thieme Verlag KG, pp. 403-442., (10.1055/sos-SD-135-00173)
• Wirth, T. 2017. 4.4.19.4 Silyl Sulfides and Selenides. In: Science of Synthesis Knowledge Updates 2017/1., Vol. 1. Georg Thieme Verlag KG, pp. 189-202., (10.1055/sos-SD-104-00365)
• Wirth, T. and Singh, F. V. 2015. Synthesis by substitution of other halogens. In: Science of Synthesis Knowledge Updates: 2015/2. Thieme, pp. 407-414.
• Wirth, T. and Singh, F. V. 2015. Synthesis by substitution of oxygen functionalities. In: Science of Synthesis Knowledge Updates: 2015/2. Thieme, pp. 415-435.
• Wirth, T. and Farid, U. 2012. Stereoselective synthesis with hypervalent iodine reagents. In: Christmann, M. and Bräse, S. eds. Asymmetric Synthesis II. Wiley-VCH, pp. 197-203.
• Singh, F. V. and Wirth, T. 2011. Selenium compounds as ligands and catalysts. In: Wirth, T. ed. Organoselenium Chemistry: Synthesis and Reactions. Weinheim: Wiley-VCH, pp. 321-360.
• Freudendahl, D. M. and Wirth, T. 2011. New selenium electrophiles and their reactivity. In: Woollins, J. D. and Laitinen, R. eds. Selenium and Tellurium Chemistry: From Small Molecules to Biomolecules and Materials. London: Springer, pp. 41-56.
• Rasheed, M., Elmore, S. C. and Wirth, T. 2011. Asymmetric reactions in flow reactors. In: Gruttadauria, M. and Giacalone, F. eds. Catalytic Methods in Asymmetric Synthesis: Advanced Materials, Techniques, and Applications. Hoboken: Wiley, pp. 345-371., (10.1002/9781118087992.ch8)
• Singh, F. V. and Wirth, T. 2011. Stereoselective reactions of organoselenium reagents including catalysis. In: Patai's Chemistry of Functional Groups. John Wiley & Sons, (10.1002/9780470682531.pat0573)
• Ogura, F., Otsubo, T., Wirth, T. and Khan, Z. A. 2010. Dimethyl selenoxide. In: Paquette, L. A. ed. E-EROS encyclopedia of reagents for organic synthesis. Chichester: Wiley
• Brandt, J. C. and Wirth, T. 2009. Homogeneous catalysis using microreactor technology. In: Benaglia, M. ed. Recoverable and Recyclable Catalysts. Oxford: Wiley, pp. 411-425., (10.1002/9780470682005.ch14)
• Choi, J., Shahzad, S. A. and Wirth, T. 2009. Dimethylaluminium methylselenolate. In: Paquette, L. A. ed. Encyclopedia of reagents for organic synthesis (e-EROS). Chichester: Wiley, (10.1002/047084289X.rd300.pub2)
• Marino, J. P., Holub, D. P., Shahzad, S. A. and Wirth, T. 2009. Diphenylselenium bis(trifluoroacetate). In: Paquette, L. A. ed. E-EROS Encyclopedia of Reagents for Organic Synthesis. Chichester: Wiley
• Simpkins, N. S. and Wirth, T. 2009. tert-Butyl Hypoiodite. In: Paquette, L. A. ed. Encyclopedia of Reagents for Organic Synthesis (EROS). 2nd ed.. Chichester: Wiley
• Ahmed-Omer, B. and Wirth, T. 2008. Liquid-liquid biphasic reactions. In: Wirth, T. ed. Microreactors in Organic Synthesis and Catalysis. Weinheim: Wiley-VCH, pp. 122-139., (10.1002/9783527622856.ch4)
• Maruoka, K., Yamamoto, H., Wirth, T. and Khan, Z. A. 2008. Diisobutylaluminium phenyl selenide. In: Paquette, L. A. ed. e-EROS encyclopedia of reagents for organic synthesis. Chichester: Wiley

Books

• Wirth, T. ed. 2011. Organoselenium chemistry: Synthesis and reactions. Weinheim: Wiley-VCH.
• Wirth, T. ed. 2008. Microreactors in organic synthesis and catalysis. Weinheim: Wiley-VCH.

Conferences

• Wirth, T. 2008. Enhancement of reaction rates by segmented flow technique: New aspects for organic synthesis. Presented at: 1st SynTOP conference, Potsdam, Germany, 1-13 June 2008Smart synthesis and technologies for organic processes : 1st SynTOP conference, Potsdam, June 11 - 13, 2008. VDI-Berichte Vol. 2039. Düsseldorf: VDI-Verl. pp. 103-104.

• Mizar, P. and Wirth, T. 2014. Flexible stereoselective functionalizations of ketones through umpolung with hypervalent iodine reagents. Angewandte Chemie International Edition 53(23), pp. 5993-5997. (10.1002/anie.201400405)
• Watts, K., Baker, A. R. and Wirth, T. 2014. Electrochemical synthesis in microreactors. Journal of Flow Chemistry 4(1), pp. 2-11. (10.1556/JFC-D-13-00030)
• Singh, F. V. and Wirth, T. 2014. Hypervalent iodine-catalyzed oxidative functionalizations including stereoselective reactions. Chemistry - An Asian Journal 9(4), pp. 950-971. (10.1002/asia.201301582)
• Farid, U., Malmedy, F., Claveau, R., Albers, L. and Wirth, T. 2013. Stereoselective rearrangements with chiral hypervalent iodine reagents. Angewandte Chemie - International Edition 52(27), pp. 7018-7022. (10.1002/anie.201302358)
• Farid, U. and Wirth, T. 2012. Highly stereoselective metal-free oxyaminations using chiral hypervalent iodine reagents. Angewandte Chemie. International Edition 51(14), pp. 3462-3465. (10.1002/anie.201107703)
• Schäfer, S. and Wirth, T. 2010. A versatile and highly reactive polyfluorinated hypervalent iodine(III) compound. Angewandte Chemie. International Edition 49(15), pp. 2786-2789. (10.1002/anie.200907134)
• Shahzad, S. A. and Wirth, T. 2009. Fast synthesis of benzofluorenes by selenium-mediated carbocyclizations. Angewandte Chemie. International Edition 48(14), pp. 2588-2591. (10.1002/anie.200806148)
• Farooq, U., Shah, A. and Wirth, T. 2009. Hypervalent Bromine Compounds: Smaller, More Reactive Analogues of Hypervalent Iodine Compounds. Angewandte Chemie - International Edition 48(6), pp. 1018-1020. (10.1002/anie.200805027)
• Freudendahl, D. M., Santoro, S., Shahzad, S. A., Santi, C. and Wirth, T. 2009. Green Chemistry with Selenium Reagents: Development of Efficient Catalytic Reactions. Angewandte Chemie - International Edition 48(45), pp. 8409-8411. (10.1002/anie.200903893)
• Richardson, R. D., Zayed, J. M., Altermann, S., Smith, D. and Wirth, T. 2007. Tetrafluoro-IBA and -IBX: Hypervalent Iodine Reagents. Angewandte Chemie - International Edition 46(34), pp. 6529-6532. (10.1002/anie.200702313)
• Wirth, T. 2005. Hypervalent iodine chemistry in synthesis: Scope and new directions. Angewandte Chemie - International Edition 44(24), pp. 3656-3665. (10.1002/anie.200500115)