{"id":45,"date":"2014-07-10T21:48:18","date_gmt":"2014-07-10T21:48:18","guid":{"rendered":"http:\/\/blogs.cardiff.ac.uk\/wirth\/?page_id=45"},"modified":"2026-09-03T13:34:04","modified_gmt":"2026-09-03T13:34:04","slug":"publications-2013","status":"publish","type":"page","link":"https:\/\/blogs.cardiff.ac.uk\/wirth\/publications-2013\/","title":{"rendered":"Publications (all)"},"content":{"rendered":"
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      1. “Nucleophilic Additions to Acceptor-Substituted 2-Vinylindoles”\r\nS. Blechert, T. Wirth, Tetrahedron Lett.<\/em> 1991<\/strong>, 32<\/em>, 7237 – 7240.<\/li>\r\n \t
      2. “Proton-induced Diels-Alder Reactions of 2-Vinylindoles”\r\nS. Blechert, T. Wirth, Tetrahedron Lett.<\/em> 1992<\/strong>, 33<\/em>, 6621 – 6624.<\/li>\r\n \t
      3. “Synthesis of 2,3-Disubstituted Indoles”\r\nT. Wirth, S. Blechert, Synlett <\/em>1994<\/strong>, 717 – 718.<\/li>\r\n \t
      4. “Direct Asymmetric alpha-Alkylation of Phenylalanine Derivatives Using No External Chiral Source”\r\nT. Kawabata, T. Wirth, K. Yahiro, H. Suzuki, K.Fuji, J. Am. Chem. Soc. <\/em>1994<\/strong>, 116<\/em>, 10809 – 10810.<\/li>\r\n \t
      5. “Domino Reactions – New Concepts in the Synthesis of Indole Alkaloids and Other Polycyclic Indole Derivatives”\r\nS. Blechert, R. Knier, H. Schroers, T. Wirth, Synthesis <\/em>1995<\/strong>, 592 – 604.<\/li>\r\n \t
      6. “Asymmetric Reaction of Arylalkenes with Diselenides”\r\nT. Wirth, Angew. Chem. <\/em>1995<\/strong>, 107<\/em>, 1872 – 1873; Angew. Chem. Int. Ed. Engl. <\/em>1995<\/strong>, 34<\/em>, 1726 – 1728.<\/li>\r\n \t
      7. “Enantioselective Alkylation of Aldehydes Catalyzed by New Chiral Diselenides”\r\nT. Wirth, Tetrahedron Lett.<\/em> 1995<\/strong>, 36<\/em>, 7849 – 7852.<\/li>\r\n \t
      8. “Memory of Chirality: Direct Asymmetric alpha-Alkylation of Phenylalanine Derivatives”\r\nT. Kawabata, T. Wirth, K. Yahiro, H. Suzuki, K.Fuji, ICR Ann. Rep.<\/em> 1996<\/strong>, 3<\/em>, 36 –\u00a037.<\/li>\r\n \t
      9. “‘New’ Reagents for the ‘Old’ Pinacol Coupling Reaction”\r\nT. Wirth, Angew. Chem.<\/em> 1996<\/strong>, 108<\/em>, 65 – 67; Angew. Chem. Int. Ed. Engl. <\/em>1996<\/strong>, 35<\/em>, 61 – 63.<\/li>\r\n \t
      10. “Vom Periodensystem zum genetischen Code” (book review)\r\nT. Wirth, Nachr. Chem. Tech. Lab.<\/em> 1996<\/strong>, 44<\/em>, 407 – 408.<\/li>\r\n \t
      11. “Chiral Diselenides in the Total Synthesis of (+)-Samin”\r\nT. Wirth, K. J. Kulicke, G. Fragale, J. Org. Chem.<\/em> 1996<\/strong>, 61<\/em>, 2686 – 2689.<\/li>\r\n \t
      12. “Chiral Diselenides from Benzylamines as Catalysts in the Diethylzinc Addition to Aldehydes”\r\nT. Wirth, K. J. Kulicke, G. Fragale, Helv. Chim. Acta <\/em> 1996<\/strong>, 79<\/em>, 1957 – 1966.<\/li>\r\n \t
      13. “Bioorganische Chemie” (conference report)\r\nM. Kalesse, T. Wirth, Nachr. Chem. Tech. Lab.<\/em>1996<\/strong> , 44<\/em>, 1178 – 1181.<\/li>\r\n \t
      14. “Chiral Hypervalent Iodine Compounds”\r\nT. Wirth, U. H. Hirt, Tetrahedron: Asymmetry<\/em> 1997<\/strong>, 8<\/em>, 23 – 26.<\/li>\r\n \t
      15. “New Strategies to alpha-Alkylated alpha-Aminoacids”\r\nT. Wirth, Angew. Chem.<\/em> 1997<\/strong>, 109<\/em>, 235 – 237; Angew. Chem. Int. Ed. Engl.<\/em> 1997<\/strong>, 36<\/em>, 225 – 227.<\/li>\r\n \t
      16. “Trendbericht 1996: Metallorganische Chemie” (review)\r\nT. Wirth, Nachr. Chem. Tech. Lab. <\/em>1997<\/strong>, 45<\/em>, 148 – 152.<\/li>\r\n \t
      17. “First Total Synthesis of (+)-Membrine”\r\nT. Wirth, Liebigs Ann.\/Recueil <\/em>1997<\/strong>, 1155 – 1158.<\/li>\r\n \t
      18. “Vom Mond zur Erde: vom Selen zum Tellur” (conference report)\r\nT. Wirth, Nachr. Chem. Tech. Lab.<\/em> 1997<\/strong>, 45<\/em>, 987.<\/li>\r\n \t
      19. “Asymmetric Addition Reactions with Optimized Selenium Electrophiles”\r\nT. Wirth, G. Fragale, Chem. Eur. J. <\/em>1997<\/strong>, 3<\/em>, 1894 – 1902.<\/li>\r\n \t
      20. “Chiral Selenium Compounds: Versatile Reagents in Organic Synthesis”\r\nT. Wirth, Liebigs Ann.\/Recueil<\/em> 1997<\/strong>, 2189 – 2196.<\/li>\r\n \t
      21. “Syntheseplanung – aber wie?” (book)<\/a>\r\nT. Wirth, Spektrum Akademischer Verlag, Heidelberg 1998<\/strong>, 206 pages.<\/li>\r\n \t
      22. “Stereoselective Isoquinoline Alkaloid Synthesis with New Diselenides”\r\nT. Wirth, G. Fragale, Synthesis<\/em> 1998<\/strong>, 162 – 166.<\/li>\r\n \t
      23. “‘New’ Reagents for the ‘Old’ Pinacol Coupling Reaction” (book chapter)\r\nT. Wirth in Organic Synthesis Highlights III, Eds.: H. Waldmann, J. Mulzer, VCH, Weinheim 1998<\/strong>, 113 – 118.<\/li>\r\n \t
      24. “Catalytic Asymmetric Oxyselenenylation – Elimination Reactions using Chiral Selenium Compounds”\r\nT. Wirth, S. H\u00e4uptli, M. Leuenberger, Tetrahedron: Asymmetry <\/em>1998<\/strong>, 9<\/em>, 547 – 550.<\/li>\r\n \t
      25. “Mechanistic Course of the Asymmetric Methoxyselenenylation Reaction”\r\nT. Wirth, G. Fragale, M. Spichty, J. Am. Chem. Soc. <\/em> 1998<\/strong>, 120<\/em>, 3376 – 3381.<\/li>\r\n \t
      26. “Chiral Diselenides in Asymmetric Cyclization Reactions”\r\nG. Fragale, T. Wirth, Eur. J. Org. Chem. <\/em>1998<\/strong>, 1361 – 1369.<\/li>\r\n \t
      27. “Glutathione Peroxidase-like Activities of Oxygen-Containing Diselenides”\r\nT. Wirth, Molecules<\/em> 1998<\/strong>, 3<\/em>, 164 – 166.<\/li>\r\n \t
      28. “Stereoselection at the Steady State: The Design of New Asymmetric Reactions”\r\nT. Wirth, Angew. Chem. <\/em>1998<\/strong>, 110<\/em>, 2179 – 2181; Angew. Chem. Int. Ed. Engl. <\/em>1998<\/strong>, 37<\/em>, 2069 – 2071.<\/li>\r\n \t
      29. “New and Efficient Selenium Reagents for Stereoselective Selenenylation Reactions”\r\nG. Fragale, T. Wirth, Chem. Commun.<\/em> 1998<\/strong>, 1867 – 1868.<\/li>\r\n \t
      30. “New Chiral Hypervalent Iodine Compunds in Asymmetric Synthesis”\r\nU. H. Hirt, B. Spingler, T. Wirth, J. Org. Chem. <\/em>1998<\/strong>, 63<\/em>, 7674 – 7679. DOI<\/a><\/li>\r\n \t
      31. “Synthesis of a New Chiral Nitrogen Containing Diselenide as a Precursor for Selenium Electrophiles”\r\nC. Santi, G. Fragale, T. Wirth, Tetrahedron: Asymmetry <\/em>1998<\/strong>, 9<\/em>, 3625 – 3628.<\/li>\r\n \t
      32. “Asymmetric Synthesis with Chiral Diselenides”\r\nT. Wirth, Phosphorus Sulfur<\/em> 1998<\/strong>, 136<\/em>, 235 – 238.<\/li>\r\n \t
      33. “Chiral Selenium Compounds in Organic Synthesis”\r\nT. Wirth, Tetrahedron<\/em> 1999<\/strong>, 55<\/em>, 1 – 28.<\/li>\r\n \t
      34. “Synthesis of Non Racemic Nitrogen Containing Diselenides as Efficient Precursor Catalysts in the Diethylzinc Addition to Benzaldehyde”\r\nC. Santi, T. Wirth, Tetrahedron: Asymmetry<\/em> 1999<\/strong>, 10<\/em>, 1019 – 1023.<\/li>\r\n \t
      35. “Stereoselective Oxidation Reactions”\r\nT. Wirth, Chimia<\/em> 1999<\/strong>, 53<\/em>, 230 – 231.<\/li>\r\n \t
      36. “Hypervalent Iodine Compounds: Recent Advances in Synthetic Applications” (review)\r\nT. Wirth, U. H. Hirt, Synthesis <\/em>1999<\/strong>, 1271 – 1287.<\/li>\r\n \t
      37. “The Origin of Stereoselectivities in Asymmetric Alkoxyselenenylations”\r\nX. Wang, K. N. Houk, M. Spichty, T. Wirth, J. Am. Chem. Soc. <\/em>1999<\/strong>, 121<\/em>, 8567 – 8576.<\/li>\r\n \t
      38. “Selenium Compounds in Chemical and Biological Oxidation Reactions”\r\nG. Fragale, S. H\u00e4uptli, M. Leuenberger, T. Wirth in New Aspects in Bioorganic Chemistry<\/em>, Eds.: U. Diederichsen, T. K. Lindhorst, L. Wessjohann, B. Westermann, VCH, Weinheim, 1999<\/strong>, 48 – 52.<\/li>\r\n \t
      39. “Organoselenium Chemistry: Modern Developments in Organic Synthesis”\r\nTop. Curr. Chem.<\/em>, Ed.: T. Wirth, 2000<\/strong>, 208.<\/em><\/a><\/li>\r\n \t
      40. “Introduction and General Aspects”\r\nT. Wirth, Top. Curr. Chem.<\/em> 2000<\/strong>, 208<\/em>, 1 – 5.<\/li>\r\n \t
      41. “New Strategies to alpha-Alkylated alpha-Aminoacids” (book chapter)\r\nT. Wirth in Organic Synthesis Highlights IV<\/em>, Ed.: H.-G. Schmalz, VCH, Weinheim, 2000<\/strong>, 26 – 33. <\/span><\/li>\r\n \t
      42. “Stereoselection at the Steady State: The Design of New Asymmetric Reactions” (book chapter)\r\nT. Wirth in Organic Synthesis Highlights IV<\/em>, Ed.: H.-G. Schmalz, VCH, Weinheim, 2000<\/strong>, 67 – 70.<\/li>\r\n \t
      43. “Oxygen and Osmium – A New Alliance for Dihydroxylations?” (Highlight)\r\nT. Wirth, Angew. Chem. <\/em>2000<\/strong>, 112<\/em>, 342 – 343; Angew. Chem. Int. Ed. Engl. <\/em>2000<\/strong>, 39<\/em>, 334 – 335.<\/li>\r\n \t
      44. Organoselenium Chemistry (book review)\r\nT. Wirth, Angew. Chem.<\/em> 2000<\/strong>, 112<\/em>, 3859 – 3860, Angew. Chem. Int. Ed. <\/em>2000<\/strong>, 39<\/em>, 1515.<\/li>\r\n \t
      45. “Tagungen im Netz: Zukunft oder Spielerei?”\r\nT. Wirth, Nachr. Chem. <\/em>2000<\/strong>, 48<\/em>, 925.<\/li>\r\n \t
      46. “Organoselenium Chemistry in Stereoselective Synthesis”\r\nT. Wirth, Angew. Chem.<\/em> 2000<\/strong>, 112<\/em>, 3890 – 3900, Angew. Chem. Int. Ed. <\/em>2000<\/strong>, 39<\/em> , 3742 – 3751.<\/li>\r\n \t
      47. “Theoretical Investigations on the Stereoselective Selenenylation Reaction of Alkenes”\r\nM. Spichty, G. Fragale, T. Wirth, J. Am. Chem. Soc.<\/em> 2000<\/strong>, 122<\/em>, 10914 – 10916.<\/li>\r\n \t
      48. “Chiral Selenium Electrophiles on Solid-Support”\r\nL. Uehlin, T. Wirth, Chimia\u00a0<\/em>2001<\/strong>, 55<\/em>, 65 – 67.<\/li>\r\n \t
      49. “Chiral Hypervalent Organo-Iodine(III) Compounds”\r\nU. H. Hirt, M. F. H. Schuster, A. N. French, O. G. Wiest, T. Wirth, Eur. J. Org. Chem. <\/em>2001<\/strong>, 1569 – 1579.<\/li>\r\n \t
      50. “Novel Polymer-Bound Chiral Selenium-Electrophiles”\r\nL. Uehlin, T. Wirth, Org. Lett.<\/em> 2001<\/strong>, 3<\/em>, 2931 – 2933.<\/li>\r\n \t
      51. “Mixed Acetals as New Precursors for Selenium Electrophiles”\r\nL. Uehlin, T. Wirth, Phosphorus Sulfur<\/em> 2001<\/strong>, 172<\/em>, 189 \u0096 194.<\/li>\r\n \t
      52. “IBX \u0096 New Reactions with an Old Reagent” (highlight)\r\nT. Wirth, Angew. Chem. <\/em>2001<\/strong>, 113<\/em>, 2893 – 2895, Angew. Chem. Int. Ed. <\/em>2001<\/strong>, 40<\/em>, 2812 – 2814.<\/li>\r\n \t
      53. “Hypervalentes Iod” (conference report)\r\nT. Wirth, Nachr. Chem. <\/em>2001<\/strong>, 49<\/em>, 1450.<\/li>\r\n \t
      54. “Reagent-Controlled Stereoselective Halolactonizations”\r\nJ. Haas, S. Piguel, T. Wirth, Org. Lett. <\/em>2002<\/strong>, 4<\/em>, 297 – 300.<\/li>\r\n \t
      55. “New and Efficient Chiral Selenium Electrophiles”\r\nL. Uehlin, G. Fragale, T. Wirth, Chem. Eur. J.<\/em> 2002<\/strong>, 8<\/em>, 1125 – 1133.<\/li>\r\n \t
      56. A cellular model for Friedreich Ataxia reveals an impaired selenium homeostasis that can be overcome by small-molecule GPX-mimetics\r\nM. Jauslin, T. Wirth, T. Meier, F. Schoumacher, Hum. Mol. Gen.<\/em> 2002<\/strong>, 11<\/em>, 3055 – 3063.<\/li>\r\n \t
      57. “Hypervalent Iodine Compounds” (book)\r\nTop. Curr. Chem.<\/em> Ed.: T. Wirth, 2003<\/strong>, 224<\/em>.<\/li>\r\n \t
      58. “Introduction and General Aspects” (book chapter)\r\nT. Wirth, Top. Curr. Chem.<\/em> 2003<\/strong>, 224<\/em>, 1 – 4.<\/li>\r\n \t
      59. “Oxidations and Rearrangements” (book chapter)\r\nT. Wirth, Top. Curr. Chem.<\/em> 2003<\/strong>, 224<\/em>, 185 – 208.<\/li>\r\n \t
      60. “Organic Synthesis Highlights V<\/em>” (book)\r\nEds.: H.-G. Schmalz, T. Wirth, VCH, Weinheim, 2003<\/strong>. online book<\/a><\/li>\r\n \t
      61. “IBX \u0096 New Reactions with an Old Reagent” (book chapter)\r\nT. Wirth in “Organic Synthesis Highlights V<\/em>“, Eds.: H.-G. Schmalz, T. Wirth, VCH, Weinheim, 2003<\/strong>, 144 – 150.<\/li>\r\n \t
      62. “Novel Lactonization with Phenonium Ion Participation Induced by Hypervalent Iodine Reagents”\r\nA. C. Boye, D. Meyer, C. K. Ingison, A. N. French, T. Wirth, Org. Lett.<\/em> 2003<\/strong>, 5<\/em>, 2157-2159. DOI<\/a><\/li>\r\n \t
      63. “Cyclopropanation of Alkenes using Hypervalent Iodine Reagents”\r\nA. S. Biland, S. Altermann, T. Wirth, ARKIVOC<\/em> 2003<\/strong>, 6<\/em>, 164-169.<\/li>\r\n \t
      64. “Direct Iodination of Alkanes”\r\nR. Montoro, T. Wirth, Org. Lett.<\/em> 2003<\/strong>, 5<\/em>, 4729-4731.<\/li>\r\n \t
      65. “Selenocyclizations: Control by Coordination and by the Counterion”\r\nS. S. Khokhar, T. Wirth, Angew. Chem.<\/em> Int. Ed. <\/em>2004<\/strong>, 43<\/em>, 631 – 633.<\/li>\r\n \t
      66. “Iodine Electrophiles in Stereoselective Reactions: Recent Developments and Synthetic Applications”\r\nA. N. French, S. Bissmire, T. Wirth, Chem. Soc. Rev. <\/em>2004<\/strong>, 33<\/strong>, 354-362.<\/li>\r\n \t
      67. “Tetrahydrofuranylation of Alcohols using Hypervalent Iodine Reagents”\r\nA. N. French, J. Cole, T. Wirth, Synlett<\/em> 2004<\/strong>, 2291-2293.<\/li>\r\n \t
      68. “Nucleophile-selective Selenocyclizations”\r\nS. S. Khokhar, T. Wirth, Eur. J. Org. Chem.<\/em> 2004<\/strong>, 4567-4581.<\/li>\r\n \t
      69. “Fluorinations of alpha-Seleno Carboxylic Acid Derivatives with Hypervalent (Difluoroiodo)toluene”\r\nM. A. Arrica, T. Wirth, Eur. J. Org. Chem.<\/em> 2005<\/strong>, 395-403.<\/li>\r\n \t
      70. “Solvent-free Reactions with Hypervalent Iodine Reagents”\r\nM. S. Yusubov, T. Wirth, Org. Lett.<\/em> 2005<\/strong>, 7<\/em>, 519-521.<\/li>\r\n \t
      71. “Synthesis of a Selenium-Substituted Diselenide”\r\nM. Cox, T. Wirth,Phosphorus Sulfur <\/em>2005<\/strong>, 180<\/em>, 659-666.<\/li>\r\n \t
      72. “Direct Bromination and Iodination of Non-activated Alkanes by Hypohalite Reagents”\r\nR. Montoro, T. Wirth, Synthesis<\/em> 2005<\/strong>, 1473-1478.<\/li>\r\n \t
      73. “Selenocarboxylic Acids and Derivatives” (book chapter)\r\nT. Wirth in Science of Synthesis, Vol. 22<\/em>, Ed. A. Charette, Thieme, Stuttgart, 2005<\/strong>, 181-212.<\/li>\r\n \t
      74. “Hypervalent Iodine Chemistry in Synthesis: Scope and New Directions”\r\nT. Wirth, Angew. Chem. <\/em>2005<\/strong>, 117<\/em>, 3722-3731; Angew. Chem. Int. Ed. <\/em>2005<\/strong>, 44<\/em>, 3656-3665.<\/li>\r\n \t
      75. “Iodine Monochloride – Amine Complexes: An Experimental and Computational Approch to New Chiral Electrophiles”\r\nJ. Haas, S. Bissmire, T. Wirth, Chem. Eur. J. <\/em>2005<\/strong>, 11<\/em>, 5777-5785.<\/li>\r\n \t
      76. “Electrochemical Generation and Catalytic Use of Selenium Electrophiles”\r\nO. Niyomura, M. Cox, T. Wirth, Synlett<\/em> 2006<\/strong>, 251-254.<\/li>\r\n \t
      77. “Enhancement of Reaction Rates by Segmented Fluid Flow in Capillary Scale Reactors”\r\nB. Ahmed, D. Barrow, T. Wirth, Adv. Synth. Catal.<\/em> 2006<\/strong>, 348<\/em>, 1043-1048.<\/li>\r\n \t
      78. “Hypervalent Iodine goes Catalytic”\r\nR. D. Richardson, T. Wirth, Angew. Chem. <\/em>2006<\/strong>, 118<\/em>, 4510-4512; Angew. Chem. Int. Ed.<\/em> 2006<\/strong>, 45<\/em>, 4402-4404.<\/li>\r\n \t
      79. “(S,S)-Bis[2-(1-hydroxypropyl)phenyl] diselenide”\r\nT. Wirth in Electronic Encyclopedia of Reagents for Organic Synthesis, Ed. L. A. Paquette, John Wiley & Sons, 2006 DOI<\/a><\/li>\r\n \t
      80. “Simple Direct Synthesis of [Bis(trifluoroacetoxy)iodo]arenes”\r\nT. K. Page, T. Wirth, Synthesis<\/em> 2006<\/strong>, 3153-3155.<\/li>\r\n \t
      81. “Selenium”\r\nT. Wirth in Comprehensive Organometallic Chemistry III (COMC-3), Eds.: R. H. Crabtree, D. M. P. Mingos, P. Knochel, Elsevier, London, Vol. 9, 457-500.<\/li>\r\n \t
      82. “New Developments with Chiral Electrophilic Selenium Reagents”\r\nD. M. Browne, T. Wirth, Curr. Org. Chem<\/em>. 2006<\/strong>, 10, 1893-1903.<\/li>\r\n \t
      83. “Stereoselective Addition Reactions with Chalcogen Electrophiles”\r\nF. W. B\u00fcrgler, G. Fragale, T. Wirth, ARKIVOC<\/em> 2007<\/strong>, 21-28. PDF<\/a><\/li>\r\n \t
      84. “Enantioselective ?-Oxytosylation of Ketones Catalysed by Iodoarenes”\r\nR. D. Richardson, T. K. Page, S. Altermann, S. M. Paradine, A. N. French, T. Wirth, Synlett<\/em> 2007<\/strong>, 538-542. DOI<\/a><\/li>\r\n \t
      85. “Advanced Organic Synthesis using Microreactor Technology”\r\nB. Ahmed, J. C. Brandt, T. Wirth, Org. Biomol. Chem. <\/em> 2007<\/strong>, 5, 733-740. DOI<\/a><\/li>\r\n \t
      86. “Hypervalent Iodine-Mediated Aziridination of Alkenes: Mechanistic Insights and Requirements for Catalysis”\r\nR. D. Richardson, M. Desaize, T. Wirth, Chem. Eur. J. <\/em> 2007<\/strong>, 13<\/em>, 6745-6754. DOI<\/a><\/li>\r\n \t
      87. “Tetrafluoro IBA and IBX: New Hypervalent Iodine Reagents”\r\nR. D. Richardson, J. M. Zayed, S. Altermann, D. Smith, T. Wirth, Angew. Chem. Int. Ed. <\/em> 2007<\/strong>, 46<\/em>, 6649-6652. DOI<\/a> Featured in SYNFORM<\/a><\/li>\r\n \t
      88. “Catalytic Use of Selenium Electrophiles in Cyclizations”\r\nD. M. Browne, O. Niyomura, T. Wirth, Org. Lett. <\/em> 2007<\/strong>, 9<\/em>, 3169-3171. DOI<\/a><\/li>\r\n \t
      89. “Cyclic Alkanesulfenic Acid Derivatives”\r\nT. Wirth, Science of Synthesis Vol. 39, 2007<\/strong>, 879-884.<\/li>\r\n \t
      90. “Alkaneselenenic Acids and Acyclic Derivatives”\r\nT. Wirth, Science of Synthesis Vol. 39, 2007<\/strong>, 1005-1012.<\/li>\r\n \t
      91. “Cyclic Alkaneselenenic Acid Derivatives”\r\nT. Wirth, Science of Synthesis Vol. 39, 2007<\/strong>, 1093-1096.<\/li>\r\n \t
      92. “Alkanetelluric Acids and Acyclic Derivatives”\r\nT. Wirth, Science of Synthesis Vol. 39, 2007<\/strong>, 1193-1196.<\/li>\r\n \t
      93. Cyclic Alkanetelluric Acids Derivatives”\r\nT. Wirth, Science of Synthesis Vol. 39, 2007<\/strong>, 1243-1244.<\/li>\r\n \t
      94. “Effect of Segmented Fluid Flow, Sonication and Phase Transfer Catalysis on Biphasic Reactions in Capillary Microreactors”\r\nB. Ahmed-Omer, D. Barrow, T. Wirth, Chem. Eng. J. <\/em> 2008<\/strong>, 135S<\/em>, S280-S283. DOI<\/a><\/li>\r\n \t
      95. “Microreactors in Organic Chemistry and Catalysis<\/a>” (book)\r\nEd.: T. Wirth, Wiley-VCH, 2008<\/strong>.<\/li>\r\n \t
      96. “Liquid – Liquid Biphasic Reactions” (book chapter)\r\nB. Ahmed-Omer, T. Wirth in Microreactors in Organic Chemistry and Catalysis, Ed.: T. Wirth, Wiley-VCH, Weinheim, 2008<\/strong>, 122-139.<\/li>\r\n \t
      97. “Catalytic addition-elimination reactions towards butenolides”\r\nD. M. Browne, O. Niyomura, T. Wirth, Phosphorus Sulfur<\/em> 2008<\/strong>, 183<\/em>, 1026-1035. DOI<\/a><\/li>\r\n \t
      98. “Tetraazafulvalene: Organisches Natrium”\r\nR. D. Richardson, T. Wirth, Chem. unserer Zeit<\/em> 2008<\/strong>, 42<\/em>, 190-191. DOI<\/a><\/li>\r\n \t
      99. “Diisobutylaluminium Phenyl Selenide”\r\nZ. A. Khan, T. Wirth in Electronic Encyclopedia of Reagents for Organic Synthesis, Ed. L. A. Paquette, John Wiley & Sons, 2008<\/strong>. DOI<\/a><\/li>\r\n \t
      100. “Dimethyl Selenoxide”\r\nZ. A. Khan, T. Wirth in Electronic Encyclopedia of Reagents for Organic Synthesis, Ed. L. A. Paquette, John Wiley & Sons, 2008<\/strong>. DOI<\/a><\/li>\r\n \t
      101. “Catalytic Enantioselective \u03b1-Oxysulfonylation of Ketones Mediated by Iodoarenes”S. M. Altermann, R. D. Richardson, T. K. Page, R. K. Schmidt, E. Holland, U. Mohammed, S. M. Paradine, A. N. French, C. Richter, A. M. Bahar, B. Witulski, T. Wirth, Eur. J. Org. Chem.<\/em> 2008<\/strong>, 5315-5328. DOI<\/a><\/li>\r\n \t
      102. “Dimethylaluminum Methylselenolate”\r\nS. A. Shahzad, T. Wirth in Electronic Encyclopedia of Reagents for Organic Synthesis, Ed. L. A. Paquette, John Wiley & Sons, 2009<\/strong>, DOI<\/a><\/li>\r\n \t
      103. “Diphenylselenium Bis(trifluoroacetate)”\r\nS. A. Shahzad, T. Wirth in Electronic Encyclopedia of Reagents for Organic Synthesis, Ed. L. A. Paquette, John Wiley & Sons, 2008<\/strong>, DOI<\/a><\/li>\r\n \t
      104. “tert-Butyl Hypoiodite”\r\nT. Wirth in Electronic Encyclopedia of Reagents for Organic Synthesis, Ed. L. A. Paquette, John Wiley & Sons, 2008<\/strong>, DOI<\/a><\/li>\r\n \t
      105. “Hypervalent Iodine Reagents: Synthesis and Catalysis”\r\nT. Wirth, SIS Report No. 11,<\/em> 2008<\/strong>, 116-123.<\/li>\r\n \t
      106. “Synthesis of Indene Derivatives via Electrophilic Cyclization”\r\nZ. A. Khan, T. Wirth, Org. Lett.<\/em> 2009<\/strong>, 11<\/em>, 229-231. DOI<\/a><\/li>\r\n \t
      107. “Recent Developments in Carbocation and Onium Chemistry” (book review)\r\nT. Wirth, Angew. Chem.<\/em> 2009<\/strong>, 121<\/em>, 443; Angew. Chem. Int. Ed. <\/em> 2009<\/strong>, 48<\/em>, 435. DOI<\/a><\/li>\r\n \t
      108. “Hypervalent Bromine Compounds: Smaller, More Reactive Analogues of Hypervalent Iodine Compounds”\r\nU. Farooq, A. A. Shah, T. Wirth, Angew. Chem.<\/em> 2009<\/strong>, 121<\/em>, 1036-1038; Angew. Chem. Int. Ed. <\/em> 2009<\/strong>, 48<\/em>, 1018-1020. DOI<\/a><\/li>\r\n \t
      109. “Fast Synthesis of Benzofluorenes by Selenium Mediated Carbocyclizations”\r\nS. A. Shahzad, T. Wirth, Angew. Chem.<\/em> 2009<\/strong>, 121<\/em>, 2626-2628; Angew. Chem. Int. Ed. <\/em> 2009<\/strong>, 48<\/em>, 2588-2591. DOI<\/a><\/li>\r\n \t
      110. “Recent Advances in Organoselenium Chemistry”\r\nD. M. Freudendahl, S. A. Shahzad, T. Wirth, Eur. J. Org. Chem.<\/em> 2009<\/strong>, 1649-1664. DOI<\/a><\/li>\r\n \t
      111. “Heck Reactions using Segmented Flow Conditions”\r\nB. Ahmed-Omer, D. A. Barrow, T. Wirth, Tetrahedron Lett.<\/em> 2009<\/strong>, 50<\/em>, 3352-3355. DOI<\/a><\/li>\r\n \t
      112. “Synthesis of Chiral Acetals by Asymmetric Selenenylations”\r\nL. Uehlin, T. Wirth, Phosphorus Sulfur<\/em> 2009<\/strong>, 184<\/em>, 1374-1385. DOI<\/a><\/li>\r\n \t
      113. “Controlling Hazardous Chemicals in Microreactors: Synthesis with Iodine Azide”\r\nJ. C. Brandt, T. Wirth, Beilstein J. Org. Chem.<\/em> 2009<\/strong>, 5<\/em>, No. 30. DOI<\/a><\/li>\r\n \t
      114. “Iodoxolone-Based Hypervalent Iodine Reagents”\r\nA. A. Shah, Z. A. Khan, N. Choudhary, C. Loh\u00f6lter, S. Sch\u00e4fer, G. P. L. Marie, U. Farooq, B. Witulski, T. Wirth, Org. Lett.<\/em> 2009<\/strong>, 11<\/em>, 3578-3581. DOI<\/a><\/li>\r\n \t
      115. “Homogeneous Catalysis using Microreactor Technology”\r\nJ. C. Brandt, T. Wirth, in Recoverable and Recyclable Catalysts<\/em>, Ed.: M. Benaglia, John Wiley & Sons, 2009<\/strong>, 411-425.<\/li>\r\n \t
      116. “Classics in Stereoselective Synthesis” (book review)\r\nT. Wirth, Chemistryworld<\/em>, November 2009<\/strong>, 63.<\/li>\r\n \t
      117. “Green Chemistry with Selenium Reagents: Development of Efficient Catalytic Reactions”\r\nD. M. Freudendahl, S. Santoro, S. A. Shahzad, C. Santi, T. Wirth, Angew. Chem.<\/em> 2009<\/strong>, 121<\/em>, 8559-8562; Angew. Chem. Int. Ed. <\/em> 2009<\/strong>, 48<\/em>, 8409-8411. DOI<\/a><\/li>\r\n \t
      118. “Authorprofile: Thomas Wirth”\r\nAngew. Chem.<\/em> 2010<\/strong>, 122<\/em>, 1570; DOI<\/a> Angew. Chem. Int. Ed. <\/em> 2010<\/strong>, 49<\/em>, 1528. DOI<\/a><\/li>\r\n \t
      119. “Synthesis of new Enantiomerically pure Organoiodine Catalysts and their Application in the \u03b1-Functionalization of Ketones”\r\nU. Farooq, S. Sch\u00e4fer, A. A. Shah, D. M. Freudendahl, T. Wirth, Synthesis<\/em> 2010<\/strong>, 1023-1029. DOI<\/a><\/li>\r\n \t
      120. “Selenium-Mediated Synthesis of Biaryls through Rearrangement”\r\nS. A. Shahzad, C. Vivant, T. Wirth, Org. Lett.<\/em> 2010<\/strong>, 12<\/em>, 1364-1367. DOI<\/a><\/li>\r\n \t
      121. “A New Versatile and Highly Reactive Polyfluorinated Hypervalent Iodine(III) Compound”\r\nS. Sch\u00e4fer, T. Wirth, Angew. Chem.<\/em> 2010<\/strong>, 122<\/em>, 2846-2850; DOI<\/a> Angew. Chem. Int. Ed. <\/em> 2010<\/strong>, 49<\/em>, 2786-2789. DOI<\/a><\/li>\r\n \t
      122. “Diselenide- and Disulfide-Mediated Synthesis of Isocoumarins”\r\nS. A. Shahzad, C. Venin, T. Wirth, Eur. J. Org. Chem.<\/em> 2010<\/strong>, 3465-3472. DOI<\/a><\/li>\r\n \t
      123. “Synthesis of New Sulfoxide-Containing Diselenides and Unexpected Cyclization Reactions to 2,3-Dihydro-1,4-benzoselenothiine 1-Oxides”\r\nD. M. Freudendahl, M. Iwaoka, T. Wirth, Eur. J. Org. Chem.<\/em> 2010<\/strong>, 3934-3944. DOI<\/a><\/li>\r\n \t
      124. “Triptycene Derivatives: Synthesis and Applications”\r\nL. Zhao, Z. Li, T. Wirth, Chem. Lett.<\/em> 2010<\/strong>, 39<\/em>, 658-667. DOI<\/a><\/li>\r\n \t
      125. “Hypervalent Iodine Chemistry \u2013 Recent Advances and Applications”\r\nS. Quideaux, T. Wirth, Tetrahedron<\/em> 2010<\/strong>, 66<\/em>, 5737-5738. DOI<\/a><\/li>\r\n \t
      126. “New Chiral Hypervalent Iodine(V) Compounds as Stoichiometric Oxidants”\r\nS. M. Altermann, S. Sch\u00e4fer, T. Wirth, Tetrahedron<\/em> 2010<\/strong>, 66<\/em>, 5902-5907. DOI<\/a><\/li>\r\n \t
      127. “Novel Cyclization Cascades to Functionalized Indanes and Tetrahydronaphthalenes”\r\nZ. A. Khan, M. Iwaoka, T. Wirth, Tetrahedron<\/em> 2010<\/strong>, 66<\/em>, 6639-6646. DOI<\/a><\/li>\r\n \t
      128. “Molecular imprinted polymers binding low functionality templates”\r\nY. Luk, C. J. Allender, T. Wirth, Tetrahedron Lett.<\/em> 2010<\/strong>, 51<\/em>, 5883-5885. DOI<\/a><\/li>\r\n \t
      129. “Safe and Efficient Ritter Reactions in Flow”\r\nJ. C. Brandt, S. C. Elmore, R. I. Robinson, T. Wirth, Synlett<\/em> 2010<\/strong>, 3099-3103. DOI<\/a><\/li>\r\n \t
      130. “Preparation of Novel Chiral Non-Racemic Diselenides and Applications in Asymmetric Synthesis”\r\nL. Zhao, Z. Li, T. Wirth, Eur. J. Org. Chem.<\/em> 2011<\/strong>, 176-182. DOI<\/a><\/li>\r\n \t
      131. “Siegfried Blechert: A Tribute”\r\nT. Wirth, Arkivoc<\/em> 2011<\/strong>, (iv)<\/em>, 1 \u2013 5. PDF<\/a><\/li>\r\n \t
      132. “Intelligent Microflow: Development of Self-Optimizing Reaction Systems”\r\nM. Rasheed, T. Wirth, Angew. Chem.<\/em> 2011<\/strong>, 123<\/em>, 374-376. DOI<\/a> Angew. Chem. Int. Ed. <\/em>2011<\/strong>, 50<\/em>, 357-358. DOI<\/a><\/li>\r\n \t
      133. “Multistep reactions using microreactor chemistry”\r\nB. Ahmed-Omer, D. A. Barrow, T. Wirth, Arkivoc<\/em> 2011<\/strong>, (iv)<\/em>, 26-36. PDF<\/a><\/li>\r\n \t
      134. “Asymmetric reactions in flow reactors”\r\nM. Rasheed, S. C. Elmore, T. Wirth, in Catalytic Methods in Asymmetric Synthesis<\/em>, Eds.: M. Gruttadauria, F. Giacalone, John Wiley & Sons, 2011<\/strong>, 345-371.<\/em><\/li>\r\n \t
      135. “Fast optimisation of a Diels-Alder reaction in a flow microreactor by in-line HPLC analysis”\r\nM. Rasheed, T. Wirth, Chem. Today<\/em> 2011<\/strong>, 29<\/em>, 54-56. INFO<\/a><\/li>\r\n \t
      136. “A practical microreactor for electrochemistry in flow”\r\nK. Watts, W. Gattrell, T. Wirth, Beilstein J. Org. Chem.<\/em> 2011<\/strong>, 7<\/em>, 1108-1114. PDF<\/a><\/li>\r\n \t
      137. “New Selenium Electrophiles and Their Reactivity”\r\nD. M. Freudendahl, T. Wirth, in Selenium and Tellurium Chemistry<\/em>, Eds.: J. D. Woolins, R. S. Laitinen, Springer, 2011<\/strong>, 41-55. INFO<\/a> PDF<\/a><\/li>\r\n \t
      138. “Asymmetric Methoxyselenenylations with Novel Chiral Selenium Electrophiles”\r\nL. Zhao, Z. Li, T. Wirth, Eur. J. Org. Chem.<\/em> 2011<\/strong>, 7080-7082. DOI<\/a><\/li>\r\n \t
      139. “Organoselenium Chemistry”\r\nEd. T. Wirth, Wiley-VCH, 2011<\/strong> Book at WILEY-VCH<\/a><\/li>\r\n \t
      140. “Selenium Compounds as Ligands and Catalysts”\r\nF. V. Singh, T. Wirth, in Organoselenium Chemistry<\/em> Ed.: T. Wirth, Wiley-VCH, 2011<\/strong> 321-360.<\/li>\r\n \t
      141. “Selenium-catalyzed Regioselective Cyclization of Unsaturated Carboxylic Acids Using Hypervalent Iodine Oxidants”\r\nF. V. Singh, T. Wirth, Org. Lett.<\/em>, 2011<\/strong>, 13<\/em>, 6504-6507. DOI<\/a><\/li>\r\n \t
      142. Ritter Reactions in Flow\r\nL. Audiger, K. Watts, S. C. Elmore, R. I. Robinson, T. Wirth, ChemSusChem<\/em> 2012<\/strong>, 5<\/em>, 257-260. DOI<\/a><\/li>\r\n \t
      143. Flow Chemistry: Enabling Technology in Drug Discovery and Process Research\r\nT. Wirth, ChemSusChem<\/em> 2012<\/strong>, 5<\/em>, 215-216. DOI<\/a><\/li>\r\n \t
      144. Opening up the World of Chemistry\r\nR. Mart\u00ednez-M\u00e1\u00f1ez, T. Wirth, ChemistryOpen<\/em> 2012<\/strong>, 1<\/em>, 4. DOI<\/a><\/li>\r\n \t
      145. Highly Stereoselective Metal-Free Oxyaminations Using Chiral Hypervalent Iodine Reagents\r\nU. Farid, T. Wirth, Angew. Chem.<\/em> 2012<\/strong>, 124<\/em>, 3518-3522; DOI<\/a> Angew. Chem. Int. Ed.<\/em>, 2012<\/strong>, 51<\/em>, 3462-3465. DOI<\/a><\/li>\r\n \t
      146. Stereoselective reactions of organoselenium reagents including catalysis\r\nF. V. Singh, T. Wirth, in Patai Series: Organic Selenium and Tellurium Compounds<\/em>, Vol. 3, Ed.: Z. Rappoport, John Wiley & Sons, 2012<\/strong>, 303-355. DOI<\/a><\/li>\r\n \t
      147. Selenium-containing Naphthalimides as Anticancer Agents: Design, Synthesis and Bioactivity\r\nL. Zhao, J. Li, Y. Li, J. Liu, T. Wirth, Z. Li, Bioorg. Med. Chem.<\/em> 2012<\/strong>, 20<\/em>, 2558-2563. DOI<\/a><\/li>\r\n \t
      148. Hypervalent Iodine Mediated Oxidative Cyclization of o-Hydroxystilbenes into Benzo- and Naphthofurans\r\nF. V. Singh, T. Wirth, Synthesis<\/em> 2012<\/strong>, 44<\/em>, 1171-1177. DOI<\/a><\/li>\r\n \t
      149. Selenenylations of alkenes with styrene nucleophiles\r\nE. Gabriele, F. V. Singh, D. M. Freudendahl, T. Wirth, Tetrahedron<\/em> 2012<\/strong>, 68<\/em>, 10573-10576. DOI<\/a><\/li>\r\n \t
      150. Stereoselective selenium catalyzed dihydroxylation and hydroxymethoxylation of alkenes\r\nC. Santi, R. Di Lorenzo, C. Tidei, L. Bagnoli, T. Wirth, Tetrahedron<\/em> 2012<\/strong>, 68<\/em>, 10530\u201310535. DOI<\/a><\/li>\r\n \t
      151. 5,6,7,8-Tetrafluoro-1-hydroxy-1-oxobenziodoxol-3(1H)one (Tetrafluoro-IBX)\r\nU. Farid, T. Wirth, Encyclopedia of Reagents for Organic Synthesis [Online]<\/em>, John Wiley & Sons Ltd., 2012<\/strong>. DOI<\/a><\/li>\r\n \t
      152. Facile Oxidative Rearrangements Using Hypervalent Iodine Reagents\r\nF. V. Singh, J. Rehbein, T. Wirth, ChemistryOpen<\/em> 2012<\/strong>, 1<\/em>, 245-250. DOI<\/a><\/li>\r\n \t
      153. Stereoselective Reactions with Hypervalent Iodine Compounds\r\nU. Farid, T. Wirth, in Asymmetric Synthesis II<\/em>, Eds.: M. Christmann, S. Br\u00e4se, Wiley VCH, 2012<\/strong>, 197 \u2013 203. Wiley<\/a><\/li>\r\n \t
      154. Hypervalent Iodine Reagents as Powerful Electrophiles\r\nM. Brown, U. Farid, T. Wirth, Synlett<\/em> 2013<\/strong>, 24<\/em>, 424-431. DOI<\/a><\/li>\r\n \t
      155. Microreactors in Organic Synthesis and Catalysis – 2nd Edition\r\nEd.: T. Wirth, Wiley-VCH, 2013<\/strong>. Wiley<\/a><\/li>\r\n \t
      156. Liquid – Liquid Biphasic Reactions” (book chapter)\r\nM. J. Hutchings, B. Ahmed-Omer, T. Wirth in Microreactors in Organic Chemistry and Catalysis – 2nd Edition, Ed.: T. Wirth, Wiley-VCH, Weinheim, 2013<\/strong>, 197-219.<\/li>\r\n \t
      157. Stereoselective Rearrangements with Chiral Hypervalent Iodine Reagents\r\nU. Farid, F. Malmedy, R. Claveau, L. Albers, T. Wirth, Angew. Chem.<\/em> 2013<\/strong>, 125<\/em>, 7156-7160; DOI<\/a> Angew. Chem. Int. Ed.<\/em> 2013<\/strong>, 52<\/em>, 7018-7022. DOI<\/a><\/li>\r\n \t
      158. Flow Chemistry in Undergraduate Organic Chemistry Education\r\nB. K\u00f6nig, P. Kreitmeier, P. Hilgers, T. Wirth, J. Chem. Educ.<\/em> 2013<\/strong>, 90<\/em>, 934-936. DOI<\/a><\/li>\r\n \t
      159. Hypervalent Iodine \/ TEMPO – mediated Oxidation in Flow Systems: A Fast and Efficient Protocol for Alcohol Oxidation\r\nN. Ambreen, R. Kumar, T. Wirth, Beilstein J. Org. Chem.<\/em> 2013<\/strong>, 9<\/em>, 1437-1442. DOI<\/a><\/li>\r\n \t
      160. Flow Synthesis of Symmetrical Di- and Trisulfides using Phase-Transfer Catalysis\r\nA. Baker, M. Graz, R. Saunders, G. J. S. Evans, S. Kaul, T. Wirth, J. Flow Chem.<\/em> 2013<\/strong>, 3<\/em>, 118-121. DOI<\/a><\/li>\r\n \t
      161. Current research on mimics and models of selenium-containing antioxidants\r\nB. J. Bhuyan, D. S. Lamani, G. Mugesh, T. Wirth, in Handbook of Chalcogen Chemistry<\/em>, Eds.: F. A. Devillanova, W. W. du Mont, RSC, 2013<\/strong>, Vol. 2<\/em>, 25-46. RSC<\/a><\/li>\r\n \t
      162. Oxidative Rearrangements with Hypervalent Iodine Reagents\r\nF. V. Singh, T. Wirth, Synthesis<\/em> 2013<\/strong>, 45<\/em>, 2499-2511. DOI<\/a><\/li>\r\n \t
      163. Efficient Terpene Synthase Catalysis by Extraction in Flow\r\nO. Casc\u00f3n, G. Richter, R. K. Allemann, T. Wirth, ChemPlusChem<\/em> 2013<\/strong>, 78<\/em>, 1334-1337. DOI<\/a><\/li>\r\n \t
      164. Difluoro- and Trifluoromethylation of Electron-deficient Alkenes in an Electrochemical Microreactor\r\nK. Arai, K. Watts, T. Wirth, ChemistryOpen<\/em> 2014<\/strong>, 3<\/em>, 23-28. DOI<\/a><\/li>\r\n \t
      165. Hypervalent Iodine-Catalyzed Oxidative Functionalizations including Stereoselective Reactions\r\nF. V. Singh, T. Wirth, Chem. Asian J.<\/em> 2014<\/strong>, 9<\/em>, 950-971. DOI<\/a><\/li>\r\n \t
      166. Electrochemical Synthesis in Microreactors\r\nK. Watts, A. Baker, T. Wirth, J. Flow Chem.<\/em> 2014<\/strong>, 4<\/em>, 2-11. DOI<\/a><\/li>\r\n \t
      167. Safe Generation and Direct Use of Diazoesters in Flow Chemistry\r\nS. T. R. M\u00fcller, D. Smith, P. Hellier, T. Wirth, Synlett<\/em> 2014<\/strong>, 25<\/em>, 871-875. DOI<\/a> Highlighted in<\/strong> Org. Process Res. Dev.<\/em> 2014<\/strong>, 18<\/em>, 840<\/a>. Featured on the\u00a0<\/strong>Organic Chemistry Portal<\/a><\/li>\r\n \t
      168. Oxidative Functionalization with Hypervalent Halides\r\nF. V. Singh, T. Wirth, in: G. A. Molander, P. Knochel (eds.), Comprehensive Organic Synthesis<\/em>, 2nd edition, Vol 7, Oxford: Elsevier; 2014<\/strong>, 880-933. DOI<\/a><\/li>\r\n \t
      169. Flexible Stereoselective Functionalizations of Ketones through Umpolung with Hypervalent Iodine Reagents\r\nP. Mizar, T. Wirth, Angew. Chem.<\/em> 2014<\/strong>, 126<\/em>, 6103-6107; DOI<\/a> Angew. Chem. Int. Ed.<\/em>, 2014<\/strong>, 53<\/em>, 5993-5997. DOI<\/a><\/li>\r\n \t
      170. Synthesis and Antioxidant Activities of Novel Chiral Ebselen Analogues\r\nM. Elsherbini, W. S. Hamama, H. H. Zoorob, D. Bhowmick, G. Mugesh, T. Wirth, Heteroatom Chem.<\/em> 2014<\/strong>, 25<\/em>, 320-325. DOI<\/a><\/li>\r\n \t
      171. Enantioselective Diamination with Novel Chiral Hypervalent Iodine Catalysts\r\nP. Mizar, A. Laverny, M. El-Sherbini, U. Farid, M. Brown, F. Malmedy, T. Wirth, Chem. Eur. J.<\/em> 2014<\/strong>, 20<\/em>, 9910-9913. DOI<\/a><\/li>\r\n \t
      172. Rapid Electrochemical Deprotection of the Isonicotinyloxycarbonyl Group from Carbonates and Thiocarbonates in a Microfluidic Reactor\r\nK. Arai, T. Wirth,\u00a0Org. Process Res. Dev.<\/em>\u00a02014<\/strong>,\u00a018<\/em>, 1377-1381. DOI<\/a> Featured on the\u00a0<\/strong>Organic Chemistry Portal<\/a><\/li>\r\n \t
      173. Organocatalytic Stereoselective Iodoamination of Alkenes\r\nP. Mizar, A. Burrelli, E. G\u00fcnther, M. S\u00f6ftje, U. Farooq, T. Wirth, Chem. Eur. J.\u00a0<\/em>2014<\/strong>, 20<\/em>, 13113\u201313116. DOI<\/a><\/li>\r\n \t
      174. High-Temperature Synthesis of Amides from Alcohols or Aldehydes by Using Flow Chemistry\r\nN. Ambreen, T. Wirth, Eur. J. Org. Chem.<\/em> 2014<\/strong>, 7590-7593. DOI<\/a><\/li>\r\n \t
      175. Synthesis of Quinolinequinone Derivatives and related Carbocyclic Compounds\r\nS. A. Egu, U. C. Okoro, T. Wirth, ScienceOpen Research<\/em> 2015<\/strong> (DOI: 10.14293\/S2199-1006.1.SOR-CHEM.AALL9P.v1)\u00a0DOI<\/a><\/li>\r\n \t
      176. Diazo compounds in continuous flow technology\r\nS. T. R. M\u00fcller, T. Wirth,\u00a0ChemSusChem\u00a0<\/em>2015<\/strong>,\u00a08<\/em>,\u00a0245-250.\u00a0<\/em>DOI<\/a><\/li>\r\n \t
      177. Convenient Synthesis of Diaryliodonium Salts for the Production of [18F]F-DOPA\r\nR. Edwards, A. D. Westwell, S. Daniels, T. Wirth,\u00a0Eur. J. Org. Chem.\u00a0<\/em>2015<\/strong>, 625-630.\u00a0<\/em>DOI<\/a><\/li>\r\n \t
      178. Rapid Generation and Safe Use of Carbenes Enabled by a Novel Flow Protocol with In-line IR spectroscopy\r\nS. T. R. M\u00fcller, A. Murat, D. Maillos, P. Lesimple, P. Hellier, T. Wirth, Chem. Eur. J. <\/em>2015<\/strong>, 21<\/em>, 7016-7020.\u00a0<\/em>DOI<\/a> Featured on the\u00a0<\/strong>Organic Chemistry Portal<\/a><\/li>\r\n \t
      179. [18<\/sup>F]6-fluoro-3,4-dihydroxy- l-phenylalanine \u2013 recent modern syntheses for an elusive radiotracer\r\nR. Edwards, T. Wirth, J. Label. Compd. Radiopharm. <\/em>2015<\/strong>, 58<\/em>, 183-187. DOI<\/a><\/li>\r\n \t
      180. Synthesis of New Chiral Diaryliodonium Salts\r\nM. Brown, M. Delorme, F. Malmedy, J. Malmgren, B. Olofsson, T. Wirth, Synlett <\/em>2015<\/strong>, 26<\/em>, 1573-1577. DOI<\/a> Featured in\u00a0<\/strong>SYNFORM<\/a><\/li>\r\n \t
      181. Flow Alkylation of Thiols, Phenols, and Amines Using a Heterogenous Base in a Packed-Bed Reactor\r\nA. Baker, M. Graz, R. Saunders, G. J. S. Evans, I. Pitotti, T. Wirth, J. Flow Chem.<\/em> 2015<\/strong>, 5<\/em>, 65-68. DOI<\/a><\/li>\r\n \t
      182. Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement\r\nJ. Tancock, T. Wirth,\u00a0Molecules<\/em>\u00a02015<\/strong>, 20<\/em>,\u00a010866-10872.\u00a0DOI<\/a><\/li>\r\n \t
      183. Small Organoselenium Compounds: More than just Glutathione Peroxidase Mimics\r\nT. Wirth, Angew. Chem.<\/em> 2015<\/strong>, 127<\/em>, 10212-10214; DOI<\/a> Angew. Chem. Int. Ed.<\/em>\u00a02015<\/strong>, 54<\/em>, 10074-10076. DOI<\/a><\/li>\r\n \t
      184. Solid-Supported Iodonium Salts for Fluorinations\r\nR. Edwards, W. de Vries, A. D. Westwell, S. Daniels, T. Wirth,\u00a0Eur. J. Org. Chem.\u00a0<\/em>2015<\/strong>, 6909-6916. DOI<\/a><\/li>\r\n \t
      185. Synthesis by Substitution of Other Halogens F. V. Singh, T. Wirth, Science of Synthesis Vol. 35 (Update 2015\/2)<\/em>, 2015<\/strong>, 407-414.<\/li>\r\n \t
      186. Synthesis by Substitution of Oxygen Functionalities\r\nF. V. Singh, T. Wirth, Science of Synthesis Vol. 35 (Update 2015\/2)<\/em>, 2015<\/strong>, 415-435.<\/li>\r\n \t
      187. Safe handling of diazo reagents\u00a0through inline analytics and flow chemistry\r\nS. T. R. M\u00fcller, A. Murat, P. Hellier, T. Wirth,\u00a0Chem. Today<\/em>\u00a0<\/em>2015<\/strong><\/strong>, 33(5)<\/em>,\u00a074-77. Link to Publisher<\/a><\/li>\r\n \t
      188. Hypervalent Iodine Chemistry<\/strong>\r\nEd. T. Wirth,\u00a0Topics in Current Chemistry<\/em>\u00a02016<\/strong>, 373<\/em>.\u00a0Publisher Link<\/a><\/li>\r\n \t
      189. Asymmetric Synthesis with Hypervalent Iodine Reagents\r\nR. Kumar, T. Wirth,\u00a0Top. Curr. Chem.<\/em>\u00a02016<\/strong>,\u00a0373<\/em>, 243-262.<\/li>\r\n \t
      190. Towards a large scale approach to Milnacipran analogues using diazo compounds in flow chemistry\r\nS. T. R. M\u00fcller, A. Murat, P. Hellier, T. Wirth,\u00a0Org. Process Res. Dev.<\/em> 2016<\/strong>, 20<\/em>, 495-502. DOI<\/a><\/li>\r\n \t
      191. Thioamination of Alkenes with Hypervalent Iodine Reagents\r\nP. Mizar, R. Niebuhr, M. Hutchings, U. Farooq,\u00a0T. Wirth,\u00a0Chem. Eur. J.\u00a0<\/em>2016<\/strong>,\u00a022<\/em>, 1614-1617.\u00a0<\/em>DOI<\/a>\u00a0\"oa\"<\/a><\/li>\r\n \t
      192. Enantioselective Oxidative Rearrangements with Chiral Hypervalent Iodine Reagents\r\nM. Brown, R. Kumar, J. Rehbein, T. Wirth, Chem. Eur. J.\u00a0<\/em>2016<\/strong>,\u00a022<\/em>, 4030-4035.\u00a0<\/em>DOI<\/a>\u00a0\u00a0\"oa\"<\/a>\u00a0COVER PICTURE<\/a><\/li>\r\n \t
      193. A simple set-up for transfer hydrogenations in flow chemistry\r\nM. Hutchings, T. Wirth, Synlett<\/em> 2016<\/strong>, 27<\/em>, 1832-1835. DOI<\/a> Highlighted in Synfacts<\/a><\/strong><\/em><\/li>\r\n \t
      194. Safe use of Nitromethane for Aldol Reactions in Flow\r\nM. Hutchings, T. Wirth,\u00a0J. Flow Chem.\u00a0<\/em>2016<\/strong>,\u00a06<\/em>, 202-205. DOI<\/a><\/li>\r\n \t
      195. Ethyl lithiodiazoacetate: Extremely unstable intermediate handled efficiently in flow\r\nS. T. R. M\u00fcller, T. Hokamp, S. Ehrmann, P. Hellier, T. Wirth,\u00a0Chem. Eur. J.\u00a0<\/em>2016<\/strong>,\u00a022<\/em>, 11940-11942. DOI<\/a><\/li>\r\n \t
      196. Contrasting Frustrated Lewis Pair Reactivity with Selenium- and Boron-Based Lewis Acids\r\nL. C. Wilkins, B. A. R. G\u00fcnther, M. Walther, J. R. Lawson, T. Wirth, R. L. Melen,\u00a0Angew. Chem.<\/em> 2016<\/strong>, 128<\/em>, 11462-11465; DOI<\/a> Angew. Chem. Int. Ed.<\/em> 2016<\/strong>, 55<\/em>, 11292-11295. DOI<\/a><\/li>\r\n \t
      197. Stereoselective Ketone Rearrangements with Hypervalent Iodine Reagents\r\nF. Malmedy, T. Wirth,\u00a0Chem. Eur. J.\u00a0<\/em>2016<\/strong>,\u00a022<\/em>, 16072-16077. DOI<\/a><\/li>\r\n \t
      198. Novel Organic Synthesis through Ultrafast Chemistry\r\nT. Wirth, Angew. Chem.<\/em> 2017<\/strong>, 129<\/em>, 698-700; DOI<\/a> Angew. Chem. Int. Ed.<\/em>\u00a02017<\/strong>, 56<\/em>, 682-684. DOI<\/a><\/li>\r\n \t
      199. Optimising Terpene Synthesis with Flow Biocatalysis\r\nX. Tang, R. K. Allemann, T. Wirth,\u00a0Eur. J. Org. Chem.\u00a0<\/em>2017<\/strong>, 414-418. DOI<\/a>\u00a0 \u00a0 \u00a0 \u00a0VIDEO (2:37 min)<\/a>\u00a0 Featured on the\u00a0<\/strong>Organic Chemistry Portal <\/a><\/strong><\/li>\r\n \t
      200. Cyclization of malonate derivatives with iodine(III) reagents\r\nF. Malmedy, T. Wirth,\u00a0Eur. J. Org. Chem.\u00a0<\/em>2017<\/strong>, 786-789. DOI<\/a><\/li>\r\n \t
      201. Facile one-pot synthesis of diaryliodonium salts from arenes and aryl iodides with Oxone\r\nN. Soldatova, P. Postnikov, O. Kukurina, V. V. Zhdankin, A. Yoshimura, T. Wirth, M. S. Yusubov, ChemistryOpen<\/em> 2017<\/strong>, 6<\/em>, 18-20.\u00a0DOI<\/a><\/li>\r\n \t
      202. Iodoaminations of Alkenes\r\nP. Mizar, T. Wirth,\u00a0Synthesis\u00a0<\/em>2017<\/strong>,\u00a049<\/em>, 981-986. DOI<\/a><\/li>\r\n \t
      203. An efficient chemoenzymatic synthesis of dihydroartemisinic aldehyde\r\nM. Demiray, X. Tang, T. Wirth, J. A. Faraldos, R. K. Allemann, Angew. Chem.<\/em>\u00a02017<\/strong>,\u00a0129<\/em>, 4411-4415;\u00a0DOI<\/a>\u00a0Angew. Chem. Int. Ed.<\/em>\u00a02017<\/strong>, 56<\/em>, 4347-4350.\u00a0DOI<\/a>\u00a0 \u00a0\"oa\"<\/a><\/li>\r\n \t
      204. Enantioselective Synthesis of trans-2,3-Dihydro-1H-indoles through C\u2013H Insertion of \u03b1-Diazocarbonyl Compounds\r\nM. Santi, S. T. R. M\u00fcller, A. A. Folgueiras-Amador, A. Uttry, P. Hellier, T. Wirth,\u00a0Eur. J. Org. Chem.\u00a0<\/em>2017<\/strong>, 1889-1893. DOI<\/a><\/li>\r\n \t
      205. Silyl Sulfides and Selenides\r\nA. Baker, T. Wirth,\u00a0Science of Synthesis Knowledge Updates<\/em>,\u00a02017<\/strong>, 1<\/em>, 189-202. DOI<\/a><\/li>\r\n \t
      206. Synthesis of 1-Chloro-n-Heteroatom-Functionalized Alkanes by Addition across C=C Bonds\r\nF. V. Singh, T. Wirth,\u00a0Science of Synthesis Knowledge Updates<\/em>,\u00a02017<\/strong>, 1<\/em>, 403-442. DOI<\/a><\/li>\r\n \t
      207. Organic synthesis in flow for medicinal chemistry\r\nT. Wirth,\u00a0Bioorg. Med. Chem.<\/em> 2017<\/strong>, 25<\/em>, 6179. DOI<\/a><\/li>\r\n \t
      208. Electron-deficient Chiral Lactic Acid-based Hypervalent Iodine Reagents\r\nJ. Qurban, M. Elsherbini, T. Wirth,\u00a0J. Org. Chem.\u00a0<\/em>2017<\/strong>, 82<\/em>,\u00a011872-11876. DOI<\/a><\/li>\r\n \t
      209. An Easy-to-Machine Electrochemical Flow Microreactor: Efficient Isoindolinone Synthesis and Flow Functionalization\r\nA. A. Folgueiras-Amador, K. Philipps, S. Guilbaud, J. Poelakker, T. Wirth, Angew. Chem.<\/em>\u00a02017<\/strong>,\u00a0129<\/em>, 15648-15653;\u00a0DOI<\/a>\u00a0Angew. Chem. Int. Ed.<\/em>\u00a02017<\/strong>, 56<\/em>, 15446-15450.\u00a0DOI<\/a>\"oa\"<\/a><\/li>\r\n \t
      210. Integration of Flow Chemistry in Multistep\u00a0Syntheses, T. Wirth,\u00a0Eur. J. Org. Chem.\u00a0<\/em>2017<\/strong>, 6464. DOI<\/a><\/li>\r\n \t
      211. Guest Editor Profile, T. Wirth,\u00a0Eur. J. Org. Chem.\u00a0<\/em>2017<\/strong>, 6465. DOI<\/a><\/li>\r\n \t
      212. Acid-Catalyzed Tandem Process for the One-Pot Synthesis of Oxazolidines\r\nA. H. Aldimairi, D. W. Knight, T. Wirth, Synlett <\/em>2017<\/strong>, 28<\/em>, 2976-2978. DOI<\/a><\/li>\r\n \t
      213. Catalytic Oxidations with Hypervalent Iodine\r\nF. V. Singh, T. Wirth,\u00a0Science of Synthesis: Catalytic Oxidation in Organic Synthesis<\/em>,\u00a02017<\/strong>, 1<\/em>, 29-62. DOI<\/a><\/li>\r\n \t
      214. Perspectives in Flow Electrochemistry\r\nA. A. Folgueiras-Amador, T. Wirth, J. Flow Chem. <\/em>2017<\/strong>, 7<\/em>, 94-95. DOI\u00a0<\/a>\"oa\"<\/a><\/li>\r\n \t
      215. Synthesis of Organoselenium Compounds with Potential Biological Activities\r\nF. V. Singh, T. Wirth, in Organoselenium Compounds in Biology and Medicine: Synthesis, Biological and Therapeutic Treatments,<\/em>\u00a0Eds. V. K. Jain, K. I. Priyadarsini, The Royal Society of Chemistry, 2018<\/strong>, 77-121.<\/li>\r\n \t
      216. Catalyst- and Supporting Electrolyte-Free Electrosynthesis of Benzothiazoles and Thiazolopyridines in Continuous Flow\r\nA. A. Folgueiras-Amador, X.-Y. Qian, H.-C. Xu, T. Wirth, Chem. Eur. J. <\/em>2018<\/strong>, 24<\/em>, 487-491. DOI<\/a> Highlighted in Synfacts<\/a><\/strong><\/em><\/li>\r\n \t
      217. Reactions of 1-Arylbenziodoxolones with Azide Anion: Experimental and Computational Study of Substituent Effects\r\nM. S. Yusubov,\u00a0N. S. Soldatova, P. S. Postnikov, R. R. Valiev, D. Y. Svitich, R. Y. Yusubova, A. Yoshimura, T. Wirth,\u00a0V. V. Zhdankin,\u00a0Eur. J. Org. Chem.<\/em> 2018<\/strong>, 640-647. DOI<\/a><\/li>\r\n \t
      218. Iodine Monoacetate for Efficient Oxyiodinations of Alkenes and Alkynes\r\nT. Hokamp, A. T. Storm, M. Yusubov, T. Wirth, Synlett <\/em>2018<\/strong>, 29<\/em>,\u00a0415-418. DOI<\/a><\/li>\r\n \t
      219. One-pot synthesis of diaryliodonium salts from arenes and aryl iodides with Oxone\u2013sulfuric acid\r\nN. Soldatova, P. Postnikov, O. Kukurina, V. V. Zhdankin, A. Yoshimura, T. Wirth, M. S. Yusubov,\u00a0Beilstein J. Org. Chem.<\/em> 2018<\/strong>, 14<\/em>, 849-855. DOI<\/a><\/li>\r\n \t
      220. Concise Synthesis of Artemisinin from a Farnesyl Diphosphate Analogue\r\nX. Tang, M. Demiray, R. K. Allemann, T. Wirth,\u00a0Bioorg. Med. Chem.<\/em> 2018<\/strong>, 26<\/em>,\u00a01314-1319. DOI<\/a><\/li>\r\n \t
      221. Selective Oxidation of Sulfides in Flow Chemistry\r\nF. Silva, A. Baker, J. Stansall, W. Michalska, M. S. Yusubov, M. Graz, R. Saunders, G. J. S. Evans, T. Wirth,\u00a0Eur. J. Org. Chem.<\/em> 2018<\/strong>, 2134-2137. DOI<\/a><\/li>\r\n \t
      222. Mechanochemical Synthesis of N-tert-Butanesulfinyl Imines Under Metal-Free Conditions\r\nM. Elsherbini, T. Wirth, Tetrahedron <\/em>2018<\/strong>, 74<\/em>, 3101-3106. DOI<\/a><\/li>\r\n \t
      223. Alternative Strategies with Iodine: Fast Access to Previously Inaccessible Iodine(III) Compounds\r\nT. Hokamp, L. Mollari, L. C. Wilkins, R. L. Melen, T. Wirth, Angew. Chem.<\/em>\u00a02018<\/strong>,\u00a0130<\/em>,\u00a08438-8442;\u00a0DOI<\/a>\u00a0Angew. Chem. Int. Ed.<\/em>\u00a02018<\/strong>, 57<\/em>,\u00a08306 -8309. DOI<\/a><\/li>\r\n \t
      224. Safe use of Hazardous Chemicals in Flow\r\nMd T. Rahman, T. Wirth,Top. Heterocycl. Chem.<\/em> 2018<\/strong>, 56<\/em>, 343-373. \u00a0DOI<\/a><\/li>\r\n \t
      225. Stereoselective reactions\r\nF. V. Singh, T. Wirth, in Patai\u2019s Chemistry of Functional Groups, The Chemistry of Hypervalent Halogen Compounds\u00a0<\/em>, Eds. I. Marek, B. Olofsson, Z. Rappoport, John Wiley & Sons, Ltd: Chichester, \u00a02018<\/strong>. DOI<\/a><\/li>\r\n \t
      226. Preparation and X-ray structure of 2-iodoxybenzenesulfonic acid (IBS) \u2013 a powerful hypervalent iodine(V) oxidant\r\nI. A. Mironova, P. S. Postnikov, R. Y. Yusubova, A. Yoshimura, T. Wirth, V. V. Zhdankin, V. N. Nemykin, M. S. Yusubov,\u00a0Beilstein J. Org. Chem.<\/em> 2018<\/strong>, 14<\/em>, 1854-1858. DOI<\/a><\/li>\r\n \t
      227. Hypervalent Iodine Reagents by Anodic Oxidation: a Powerful Green Synthesis\r\nM. Elsherbini, T. Wirth, Chem. Eur. J.\u00a0<\/em>2018<\/strong>, 24<\/em>, 13399-13407.\u00a0DOI<\/a><\/li>\r\n \t
      228. Short Total Synthesis of Ajoene\r\nF. Silva, S. S. Khokhar, D. M. Williams, R. Saunders, G. J. S. Evans, M. Graz, T. Wirth, Angew. Chem.<\/em>\u00a02018<\/strong>,\u00a0130<\/em>,\u00a012470-12473;\u00a0DOI<\/a>\u00a0Angew. Chem. Int. Ed.<\/em>\u00a02018<\/strong>, 57<\/em>,\u00a012290-12293.\u00a0DOI<\/a>\"oa\"<\/a><\/li>\r\n \t
      229. Electrosynthesis in Continuous Flow\r\nA. A. Folgueiras-Amador, T. Wirth,\u00a0Science of Synthesis,\u00a0Flow Chemistry in Organic Synthesis<\/em>, 2018<\/strong>, 147-189. DOI<\/a><\/li>\r\n \t
      230. Organoselenium Chemistry\r\nF. V. Singh, T. Wirth, in\u00a0Encyclopedia of Inorganic and Bioinorganic Chemistry<\/em>, John Wiley & Sons, Ltd: Chichester,\u00a02018<\/strong>. DOI<\/a><\/li>\r\n \t
      231. Enantioselective Electrochemical Lactonization Using Chiral Iodoarenes as Mediators\r\nW.-C. Gao, Z.-Y. Xiong, S. Pirhaghani, T. Wirth,\u00a0Synthesis<\/em>\u00a02019<\/strong>, 51<\/em>, 276-284. DOI<\/a>\"oa\"<\/a><\/li>\r\n \t
      232. Selenium and Tellurium Electrophiles in Organic Synthesis\r\nF. V. Singh, T. Wirth in Selenium and Tellurium Reagents<\/em>, Eds. R. Laitinen, R. Oilunkaniemi, De Gruyter, 2019<\/strong>, pp. 243-299.\r\nF. V. Singh, T. Wirth,\u00a0Phys. Sci. Rev.<\/em>\u00a02019<\/strong>, 4<\/i>. DOI<\/a><\/li>\r\n \t
      233. Efficient Electrosynthesis of Thiazolidin-2-imines via\u00a0Oxysulfurization of Thiourea-Tethered Terminal Alkenes using the Flow Microreactor\r\nM. Islam, B. M. Kariuki, Z. Shafiq, T. Wirth, N. Ahmed, Eur. J. Org. Chem.<\/em> 2019<\/strong>, 1371-1376.\u00a0DOI<\/a><\/li>\r\n \t
      234. Selenium Reagents as Catalysts\r\nF. V. Singh, T. Wirth, Catal. Sci. Technol.<\/em> 2019<\/strong>, 9<\/em>, 1073-1091. DOI<\/a><\/li>\r\n \t
      235. Meet the Board of ChemistryOpen<\/em>: Thomas Wirth\r\nT. Wirth, ChemistryOpen<\/em> 2019<\/strong>, 8<\/em>, 251. DOI<\/a><\/li>\r\n \t
      236. Flow Synthesis of Iodonium Trifluoroacetates through Direct Oxidation of Iodoarenes by Oxone\u00ae\r\nN. S. Soldatova, P. S. Postnikov, M. S. Yusubov, T. Wirth, Eur. J. Org. Chem.<\/em> 2019<\/strong>, 2081-2088. DOI<\/a><\/li>\r\n \t
      237. Morpholin-2-one Derivatives via Intramolecular Acid-Catalyzed Hydroamination\r\nA. H. Aldimairi, D. W. Knight, T. Wirth, Synthesis<\/em>\u00a02019<\/strong>, 51<\/em>,\u00a01643-1648. DOI<\/a><\/li>\r\n \t
      238. Metal-Free Tandem Rearrangement\/Lactonization: Access to 3,3-Disubstituted Benzofuran-2-(3H<\/em>)-ones\r\nM. Santi, D. M. C. Ould, J. Wenz, Y. Soltani, R. L. Melen, T. Wirth, Angew. Chem.<\/em>\u00a02019<\/strong>,\u00a0131<\/em>,\u00a07943-7947;\u00a0DOI<\/a>\u00a0Angew. Chem. Int. Ed.<\/em>\u00a02019<\/strong>, 58<\/em>,\u00a07861-7865.\u00a0DOI<\/a><\/li>\r\n \t
      239. Efficient Flow Electrochemical Alkoxylation of Pyrrolidine-1-carbaldehyde\r\nN. Amri, R. A. Skilton, D. Guthrie, T. Wirth, Synlett<\/em>\u00a02019<\/strong>, 30<\/em>, 1183-1186.\u00a0DOI<\/a><\/li>\r\n \t
      240. 2-Iodoxybenzoic acid ditriflate: the most powerful hypervalent iodine(V) oxidant\r\nM. S. Yusubov, N. S. Soldatova, P. Postnikov, R. R. Valiev, A. Yoshimura, T. Wirth, V. Nemykin, V. V. Zhdankin, Chem. Commun.<\/em> 2019<\/strong>, 55<\/em>, 7760-7763. \u00a0DOI<\/a>\u00a0 \u00a0Highlighted in <\/span>Chemistry World<\/a><\/strong><\/em>\u00a0\u00a0<\/span><\/li>\r\n \t
      241. Continuous Flow Electrochemical Generator of Hypervalent Iodine Reagents: Synthetic Applications\r\nM. Elsherbini, B. Winterson, H. Alharbi, A. A. Folgueiras-Amador, C. G\u00e9not,\u00a0T. Wirth, <\/strong>Angew. Chem.<\/em>\u00a02019<\/strong>,\u00a0131<\/em>,\u00a09916-9920;\u00a0DOI<\/a>\u00a0\u00a0Angew. Chem. Int. Ed.<\/em>\u00a02019<\/strong>, 58<\/em>,\u00a09811-9815. DOI<\/a> Highlighted in Synfacts<\/a><\/strong><\/em><\/li>\r\n \t
      242. Structurally Defined \u03b1-Tetralol-Based Chiral Hypervalent Iodine Reagents\r\nT. Hokamp, T. Wirth, J. Org. Chem. <\/em>2019<\/b>, 84<\/em>, 8674-8682. DOI<\/a><\/li>\r\n \t
      243. Synthesis, characterisation, and reactivity of novel pseudocyclic hypervalent iodine reagents with heteroaryl carbonyl substituents\r\nJ. Qurban, M. Elsherbini, H. Alharbi, T. Wirth, Chem. Commun.<\/em> 2019<\/strong>, 55<\/em>, 7998-8000. DOI<\/a><\/li>\r\n \t
      244. Reactions of hydrazones and hydrazides with Lewis\u00a0acidic boranes\r\nT. A. Gazis, A. Dasgupta, M. S. Hill, J. M. Rawson, T. Wirth, R. L. Melen,\u00a0Dalton Trans.\u00a0<\/em>2019<\/strong>, 48<\/em>, 12391-12395. DOI<\/a><\/li>\r\n \t
      245. \u2018Dark\u2019 Singlet Oxygen Made Easy\r\n<\/strong>M. Elsherbini, R. K. Allemann,\u00a0T. Wirth, Chem. Eur. J.<\/em>\u00a02019<\/strong>,\u00a025<\/em>, 12486-12490.\u00a0DOI<\/a>\u00a0Highlighted in OPRD<\/a><\/strong><\/em><\/li>\r\n \t
      246. Electrochemistry under Flow Conditions\r\nA. A. Folgueiras-Amador, T. Wirth in\u00a0Flow Chemistry: Integrated Approaches for Practical Applications<\/em>, Eds: S. V. Luis, E. Garcia-Verdugo, RSC Publishing,\u00a02019<\/strong>, pp. 153-198. DOI<\/a><\/li>\r\n \t
      247. Manganese-Catalyzed Electrochemical Deconstructive Chlorination of Cycloalkanols via Alkoxy Radicals\r\nB. D. W. Allen, M. D. Hareram, A. C. Seastram, T. McBride, T. Wirth, D. L. Browne, L. C. Morrill,\u00a0Org. Lett.\u00a0<\/em>2019<\/strong>,\u00a021<\/em>, 9241-9246. DOI<\/a><\/li>\r\n \t
      248. Electroorganic Synthesis under Flow Conditions\r\nM. Elsherbini,\u00a0T. Wirth,\u00a0Acc. Chem. Res.\u00a0<\/em>2019<\/strong>, 52<\/em>, 3287-3296. DOI<\/a><\/li>\r\n \t
      249. Memory of Chirality in Flow Electrochemistry: Fast Optimisation with DoE and Online 2D-HPLC\r\n<\/strong>M. Santi, J. Seitz, R. Cicala, T. Hardwick, N. Ahmed, T. Wirth,\u00a0Chem. Eur. J.\u00a0<\/em>2019<\/strong>,\u00a025<\/em>,\u00a016230-16235. DOI<\/a><\/li>\r\n \t
      250. 1,3-Carboboration of Iodonium Ylides\r\nT. A. Gazis, B. A. Mohajeri, D. Willcox, D. M. C. Ould, J. Wenz, J. M. Rawson, M. S. Hill, T. Wirth, R. L. Melen,\u00a0Chem. Commun. <\/em>2020<\/strong>, 56<\/em>,\u00a03345-3348. DOI<\/a><\/li>\r\n \t
      251. Immobilised Enzymes for Sesquiterpene Synthesis in Batch and Flow Systems\r\nD. Valikhani, P. L. Srivastava, R. K. Allemann, T. Wirth, ChemCatChem<\/em> 2020<\/strong>, 12<\/em>, 2194-2197.<\/em> DOI<\/a><\/li>\r\n \t
      252. Automated Electrochemical Selenenylations\r\nN. Amri, T. Wirth, Synthesis<\/em> 2020<\/strong>, 52<\/em>, 1751-1761. DOI<\/a><\/li>\r\n \t
      253. Short Total Synthesis of Ajoene, (E<\/i>,Z<\/i>)-4,5,9-Trithiadodeca-1,6,11-triene 9-oxide, in Batch and (E<\/i>,Z<\/i>)-4,5,9-Trithiadodeca-1,7,11-triene in Continuous Flow<\/span>\r\n<\/strong>M. Yamamoto Raynbird, F. Silva,\u00a0H. Smallman, S. S. Khokhar, D. Neef, G. J. S. Evans<\/span>,\u00a0T. Wirth, Chem. Eur. J.<\/em>\u00a02020<\/strong>,\u00a026<\/em>, 8363-8367. DOI<\/a><\/li>\r\n \t
      254. Hypervalent Iodine(III)-Catalysed Enantioselective \u03b1<\/i>-Acetoxylation of Ketones\r\n<\/strong>T. Hokamp,\u00a0T. Wirth, Chem. Eur. J.<\/em>\u00a02020<\/strong>,\u00a026<\/em>, 10417-10421.\u00a0DOI<\/a><\/li>\r\n \t
      255. Selective hydroboration – oxidation of terminal alkenes under flow conditions\r\n<\/strong>M. Elsherbini, F. Huynh, A. Dunbabin,\u00a0<\/span>R. K. Allemann,\u00a0T. Wirth, Chem. Eur. J.<\/em>\u00a02020<\/strong>,\u00a026<\/em>, 11423-11425. DOI<\/a>\u00a0Highlighted in Synfacts<\/strong><\/em><\/a>\r\n<\/span><\/span><\/li>\r\n \t
      256. Accelerating biphasic biocatalysis through new process windows\r\n<\/strong>F. Huynh, M. Tailby, A. Finniear, K. Stephens, R. K Allemann, T. Wirth, <\/strong>Angew. Chem.<\/em>\u00a02020<\/strong>,\u00a0132<\/em>, 16632-16637;\u00a0DOI<\/a>\u00a0\u00a0Angew. Chem. Int. Ed.<\/em>\u00a02020<\/strong>, 59<\/em>, 16490-16495. DOI<\/a><\/li>\r\n \t
      257. Memory of chirality in a room temperature flow electrochemical reactor\r\nT. Hardwick, R. Cicala, T. Wirth, N. Ahmed, Sci. Rep.<\/em>\u00a02020<\/strong>,\u00a010<\/em>, 16627. DOI<\/a><\/li>\r\n \t
      258. Accelerating Electrochemical Synthesis through Automated Flow: Efficient Synthesis of Chalcogenophosphites\r\nN. Amri, T. Wirth, Synlett<\/em> 2020<\/strong>, 31<\/em>, 1894-1898. DOI<\/a><\/span><\/span><\/li>\r\n \t
      259. Synthesis of Ajoene Analogues by Novel Synthetic Strategies\r\nM. Yamamoto Raynbird, S. S. Khokhar, D. Neef, G. J. S. Evans,\u00a0T. Wirth, Chem. Eur. J.\u00a0<\/em>2021<\/strong>,\u00a027<\/em>, 3008\u20133012. DOI<\/a><\/li>\r\n \t
      260. C\u2013N Axial Chiral Hypervalent Iodine Reagents: Catalytic Stereoselective \u03b1-Oxytosylation of Ketones\r\n<\/strong>H. Alharbi, M. Elsherbini, J. Qurban<\/span>,\u00a0T. Wirth, Chem. Eur. J.<\/em>\u00a02021<\/strong>,\u00a027<\/em>, 4317\u20134321. DOI<\/a><\/li>\r\n \t
      261. Chiral Triptycenes: Concepts, Progress and Prospects\r\n<\/strong>N. Khan,\u00a0T. Wirth, Chem. Eur. J.<\/em>\u00a02021<\/strong>,\u00a027<\/em>, 7059\u20137068. DOI<\/a><\/li>\r\n \t
      262. Iodine(III) Mediators in Electrochemical Batch and Flow Reactions\r\n<\/strong>T. Wirth, Curr. Opin. Electrochem.<\/em>\u00a02021<\/strong>, 28<\/em>, 100701. DOI<\/a><\/li>\r\n \t
      263. Recent Advances in Asymmetric Functionalization of Olefins Induced by Chiral Hypervalent Iodine Reagents\r\n<\/strong>H. Zhang, T. Wirth, Chin. J. Org. Chem.<\/em>\u00a02021<\/strong>, 41<\/em>, 56\u201379. DOI<\/a><\/li>\r\n \t
      264. Recent Advances in the Electrochemical Synthesis of Organosulfur Compounds\r\n<\/strong>N. Amri, T. Wirth, Chem. Rec.<\/em>\u00a02021<\/strong>, 21<\/i>, 2526\u20132537. DOI<\/a><\/li>\r\n \t
      265. Electrochemistry in Flow for Drug Discovery\r\nB. Winterson, T. Wirth, Top. Med. Chem.<\/i>\u00a02021<\/strong>,\u00a0121\u2013172. DOI<\/a><\/li>\r\n \t
      266. Reactions Promoted by Hypervalent Iodine Reagents and Boron Lewis Acids\r\nA. Dasgupta, C. Thiehoff, P. D. Newman, T. Wirth, R. L. Melen, Org.\u00a0Biomol. Chem.<\/i>\u00a02021<\/strong>, 19<\/em>, 4852\u20134865. DOI<\/a><\/li>\r\n \t
      267. Hypervalent iodine chemistry and light: photochemical reactions involving hypervalent iodine chemistry\r\n<\/strong>F. V. Singh, T. Wirth, ARKIVOC<\/i>\u00a02021<\/strong>, vii<\/em>,\u00a012\u201347. DOI<\/a><\/li>\r\n \t
      268. Flow Electrochemistry: A Safe Tool for Fluorine Chemistry\r\n<\/strong>B. Winterson, T. Renningholtz, T. Wirth, Chem. Sci.<\/i>\u00a02021<\/strong>, 12<\/i>, 9053\u20139059. DOI<\/a><\/li>\r\n \t
      269. Flow Electrosynthesis of Sulfoxides, Sulfones and Sulfoximines without Supporting Electrolytes\r\nN. Amri, T. Wirth, J. Org. Chem.<\/em>\u00a02021<\/strong>, 86<\/em>, 15961\u201315972. <\/em>DOI<\/a><\/li>\r\n \t
      270. Electrochemical Bromofunctionalization of Alkenes in a Flow Reactor\r\n<\/strong>J. Seitz, T. Wirth, Org.\u00a0<\/em>Biomol. Chem.<\/i>\u00a02021<\/strong>, 19<\/em>, 6892\u20136896. DOI<\/a><\/li>\r\n \t
      271. Hypervalent Bromine(III) Compounds: Synthesis, Applications, Prospects\r\n<\/strong>B. Winterson, T. Patra, T. Wirth, Synthesis\u00a0<\/em>2022<\/strong>, 54<\/em>, 1261\u20131271. <\/span>DOI<\/a><\/li>\r\n \t
      272. Chiral Ligands in Hypervalent Iodine Compounds: Synthesis and Structures of Binaphthyl-based \u03bb3<\/sup>-Iodanes\r\n<\/strong>H. Zhang, R. A. Cormanich,\u00a0T. Wirth, Chem. Eur. J.<\/em>\u00a02022<\/strong>, 28<\/em>,\u00a0e202103623. DOI<\/a><\/li>\r\n \t
      273. Oxidation of BINOLs by Hypervalent Iodine Reagents: Facile Synthesis of Xanthenes and Lactones\r\nH. Zhang, T. Wirth, Chem. Eur. J.\u00a0<\/em>2022<\/strong>, 28<\/em>,\u00a0e202200181. DOI<\/a><\/li>\r\n \t
      274. Zwitterionic Iodonium Species Afford Halogen Bond-Based Porous Organic Frameworks\r\nN. S. Soldatova, P. S. Postnikov, D. M. Ivanov, O. Semyonov, O. Kukurina, O. Guselnikova, Y. Yamauchi, T. Wirth, V. V. Zhdankin, M. S. Yusubov, R. M. Gomila, A. Frontera, G. Resnati, V. Yu. Kukushkin, Chem. Sci.<\/em>\u00a02022<\/strong>, 13<\/em>, 5650\u20135658.\u00a0DOI<\/a><\/li>\r\n \t
      275. Biomimetic Total Synthesis of (\u2013)-Galanthamine via Intramolecular Anodic Aryl-Phenol Coupling\r\nZ. Xiong, F. Weidlich, C. Sanchez, T. Wirth,\u00a0Org. Biomol. Chem.\u00a0<\/em>2022<\/strong>, 20<\/em>,\u00a04123\u20134127. <\/em>DOI<\/a><\/li>\r\n \t
      276. Borane promoted aryl transfer reaction for the synthesis of \u03b1-aryl functionalised \u03b2-hydroxy and \u03b2-keto esters\r\nT. Kaehler, J. Lorenz, D. M. C. Ould, D. Engl, M. Santi, L. Gierlichs, T. Wirth, R. L. Melen,\u00a0Org. Biomol. Chem.\u00a0<\/em>2022<\/strong>, 20<\/em>, 4298\u20134302. <\/em>DOI<\/a><\/li>\r\n \t
      277. Electrochemical Deconstructive Functionalization of Cycloalkanols via Alkoxy Radicals Enabled by Proton-Coupled Electron Transfer\r\nM. D. Hareram, A. A. M. A. El Gehani, J. Harnedy, A. C. Seastram, A. C. Jones, M. Burns, T. Wirth, D. L. Browne, L. C. Morrill,\u00a0Org. Lett.\u00a0<\/em>2022<\/strong>, 24<\/em>, 3890\u20133895.<\/em> DOI<\/a><\/li>\r\n \t
      278. Chiral Iodotriptycenes: Synthesis and Catalytic Applications\r\nN. Khan, T. Wirth,\u00a0ChemistryOpen<\/em> 2022<\/strong>, 11<\/em>, e202200145. DOI<\/a><\/li>\r\n \t
      279. Progress in organocatalysis with hypervalent iodine catalysts\r\nF. V. Singh, S. E. Shetgaonkar, M. Krishnan, T. Wirth,\u00a0Chem. Soc. Rev.\u00a0<\/em>2022<\/strong>, 51<\/em>, 8102\u20138139.\u00a0DOI<\/a><\/li>\r\n \t
      280. Oxidative Cleavage of Alkenes by Photosensitized Nitroarenes\r\n<\/strong>T. Patra, T. Wirth,\u00a0Angew. Chem. <\/em>2022<\/strong>, 134<\/em>,\u00a0e202213772. DOI<\/a>; \u00a0Angew. Chem. Int. Ed.<\/em> 2022<\/strong>, 61<\/em>,\u00a0e202213772. DOI<\/a><\/li>\r\n \t
      281. Two-step continuous-flow synthesis of 6-membered cyclic iodonium salts via anodic oxidation\r\n<\/strong>J. Spils, T. Wirth, B. Nachtsheim, Beilstein J. Org. Chem.<\/em> 2023<\/strong>, 19<\/em>, 27\u201332. DOI<\/a><\/li>\r\n \t
      282. Sulfur-based chiral iodoarenes: An underexplored class of chiral hypervalent iodine reagents\r\n<\/strong>M. Elsherbini, A. Osi, H. Alharbi, F. Karam, T. Wirth, Synthesis<\/i>\u00a02023<\/strong>, 55<\/em>,\u00a0307\u2013314. DOI<\/a><\/li>\r\n \t
      283. New strategies in organic electrosynthesis: general discussion\r\nM. Avanthay, J. A. Beeler, B. Batanero,\u00a0D. G. Boucher, R. C. D. Brown, V. Flexer, R. Francke, B. A. Frontana-Uribe, S. Hosseini, L. Luo, S. D. Minteer, R. Price, N. Shida, J. M. Ramos-Villasen\u0303or, T. Wirth, Faraday Discuss.<\/em>\u00a02023<\/strong>, 247<\/em>, 125\u2013131.\u00a0DOI<\/a><\/li>\r\n \t
      284. Alkene reactions with superoxide radical anions in flow electrochemistry\r\nR. Ali, T. Patra, T. Wirth, Faraday Discuss.\u00a0<\/em>2023<\/strong>, 247<\/em>, 297\u2013301.\u00a0DOI<\/a><\/li>\r\n \t
      285. Flow cells and reactor design: general discussion\r\nA. Alkayal, M. Avanthay,\u00a0B. Batanero, P. Broersen, R. C. D. Brown, L. Chen,\u00a0P.-C. Chuang,\u00a0T. Fuchigami, S. Inagi,\u00a0D. Kalyani,\u00a0K. Lam, M. Landis, T. L. Liu, M. J. Milner,\u00a0R. Price, N. Shida, T. Wirth, Faraday Discuss.\u00a0<\/em>2023<\/strong>,\u00a0247<\/em>, 333\u2013341.\u00a0DOI<\/a><\/li>\r\n \t
      286. Flow Electrochemistry for the N-Nitrosation of Secondary Amines\r\nR. Ali, R. Babaahmadi, M. Didsbury, R. Stephens, R. L. Melen,\u00a0T. Wirth, Chem. Eur. J.<\/em>\u00a02023<\/strong>, 29<\/em>,\u00a0e202300957. DOI<\/a><\/li>\r\n \t
      287. B(3,4,5-F3<\/small>H2<\/small>C6<\/small>)3<\/small> Lewis acid-catalysed C3-allylation of indoles\r\nN. Alotaibi, R. Babaahmadi, M. Pramanik, T. Kaehler, A. Dasgupta, E. Richards, A. Ariafard, T. Wirth, R. L. Melen,\u00a0Dalton Trans.<\/em>\u00a02023<\/strong>,\u00a052<\/em>, 5039\u20135043.\u00a0DOI<\/a><\/li>\r\n \t
      288. Hypervalent Iodine in Electrochemical Reactions: Advantages and Prospects\r\nT. Wirth,\u00a0SIS Lett.\u00a0<\/em>2023<\/strong>,\u00a0No.\u00a024<\/em>, 2\u20136.<\/li>\r\n \t
      289. Synthesis of Chiral Iodoaniline-Lactate Based Catalysts for the \u03b1-Functionalization of Ketones\r\nR. Alkahtani, T. Wirth,\u00a0ACS Org. Inorg. Au\u00a0<\/em>2023<\/strong>, 3<\/em>, 209\u2013216.\u00a0<\/em>DOI<\/a><\/li>\r\n \t
      290. Hypervalent Halogen Compounds in Electrochemical Reactions: Advantages and Prospects\r\nB. Winterson, D. Bhattacherjee, T. Wirth,\u00a0Adv. Synth. Catal.\u00a0<\/em>2023<\/strong>,\u00a0365<\/em>, 2676\u20132689.\u00a0<\/em>DOI<\/a><\/li>\r\n \t
      291. Isodesmic metathesis chemistry: A novel way to recycle P(V)\r\nT. Boruah, R. L. Melen, T. Wirth, Chem Catal.\u00a0<\/i>2023<\/strong>,\u00a03<\/em>, 100731. <\/em>DOI<\/a><\/li>\r\n \t
      292. Electric-field-assisted anion-\u03c0 catalysis on carbon nanotubes in electrochemical microfluidic devices\r\n<\/span>M. A\u0301. <\/span>Gutie\u0301rrez Lo\u0301pez, R. Ali, M.-L. Tan, N. Sakai, T. Wirth, S. Matile, Sci. Adv.<\/em> 2023<\/strong>, 9<\/em>, eadj5502. DOI<\/a><\/span><\/li>\r\n \t
      293. Advances in CO2<\/small> activation by frustrated Lewis pairs: from stoichiometric to catalytic reactions\r\nN. Khan, Y. van Ingen, T. Boruah, A. McLauchlan, T. Wirth, R. L. Melen, Chem. Sci.<\/em>\u00a02023<\/strong>,\u00a014<\/i>, 13661\u201313695.\u00a0DOI<\/a><\/li>\r\n \t
      294. Selected Diastereoselective Reactions: Hypervalent iodine chemistry\r\nF. V. Singh, T. Wirth in Comprehensive Chirality:\u00a0Chiral Pool and Diastereoselective Synthesis<\/em>, Ed. J. Cossy, Elsevier,\u00a02024<\/strong>,\u00a0 663\u2013679. <\/em>DOI<\/a><\/li>\r\n \t
      295. An un-forgotten classic: the nitro-Mannich reaction between nitrones and silyl nitronates catalysed by B(C6<\/small>F5<\/small>)3<\/small>\r\n<\/small><\/strong>M. Guerzoni, Y. van Ingen, R. Babaahmadi, T. Wirth, E. Richards, R. L. Melen, <\/span>Chem. Sci.<\/em> 2024<\/strong>, <\/span>15<\/em>,\u00a02648\u20132654.<\/span>\u00a0<\/span>DOI<\/a><\/li>\r\n \t
      296. B(C6<\/small>F5<\/small>)3<\/small>-Catalysed Alkylation of Imidazo[1,2-a]pyridines Using\u00a0\u03b1,\u03b2-Unsaturated Ketones\r\nN. Alotaibi, R. Babaahmadi, M. Pramanik, S. Das, B. M. Kariuki, E. Richards, T. Wirth, R. L. Melen,\u00a0Eur. J. Org. Chem.\u00a0<\/em>2024<\/strong>, 27<\/em>, e202400022. DOI<\/a><\/li>\r\n \t
      297. Biphasic Organic Synthesis with Continuous Electro-Flow\r\n<\/strong>P. Mizar, S. Arepally, T. Wirth,\u00a0Curr. Opin. Green Sust. Chem.\u00a0<\/em>2024<\/strong>, 46<\/em>, 100896.\u00a0DOI<\/a><\/li>\r\n \t
      298. Non-Conventional Methodologies for the Synthesis of N<\/em>-Nitrosamines\r\nR. Ali, C. Wolfe, T. Wirth,\u00a0Chem. Meth.\u00a0<\/em>2024<\/strong>, 4, e202300053.\u00a0DOI<\/a><\/li>\r\n \t
      299. Continuous Flow Electroselenocyclization of Allylamides and Unsaturated Oximes to Selenofunctionalized Oxazolines and Isoxazolines\r\nO. Alzaidi, T. Wirth,\u00a0ACS Org. Inorg. Au\u00a0<\/em>2024<\/strong>,\u00a04<\/em>, 350\u2013355.\u00a0<\/em>DOI<\/a><\/li>\r\n \t
      300. Diverse Reactivity of Amidinate-Supported Boron Centers with the Hypersilyl Anion and Access to a Monomeric Secondary Boron Hydride\r\nS. Pahar, Y. van Ingen, R. Babaahmadi, B. M. Kariuki, T. Wirth, E. Richards, R. L. Melen,\u00a0Inorg. Chem.\u00a0<\/em>2024<\/strong>, 63<\/em>, 8302\u20138311. DOI<\/a><\/li>\r\n \t
      301. Deville Rebooted \u2013 Practical N2<\/small>O5<\/small> Synthesis\r\nL. E. Edwards, B. M. Kariuki, M. Didsbury, C. D. Jones, T. Wirth, Chem. Commun.\u00a0<\/em>2024<\/strong>, 60<\/em>, 5920\u20135923. DOI<\/a><\/li>\r\n \t
      302. B(C6<\/small>F5<\/small>)3<\/small>-catalysed selective C\u2013H chalcogenation of arenes and heteroarenes\r\nM. Pramanik, S. Das, R. Babaahmadi, S. Pahar, T. Wirth, E. Richards, R. L. Melen,\u00a0Chem\u00a0<\/em>2024<\/strong>, 10<\/em>, 2901\u20132915<\/span>.<\/em>\u00a0DOI<\/a><\/li>\r\n \t
      303. Electrocatalytic continuous flow chlorinations with iodine(I\/III) mediators\r\nT. Patra, S. Arepally, J. Seitz, T. Wirth, Nat. Commun.\u00a0<\/em>2024<\/strong>, 15<\/i>, 6329. DOI<\/a><\/li>\r\n \t
      304. Large-Scale Methanol Production from Carbon Dioxide, Water and Electricity\r\nT. Wirth, THE CATALYST REVIEW, 2024<\/strong>, 37<\/em>, 3.<\/li>\r\n \t
      305. Flow Electrosynthesis of Phosphinamides and Phosphoramidates through P\u2013N Coupling\r\nT. Boruah, R. Ishizeki, A. Roldan, R. L. Melen, T. Wirth,\u00a0Green Chem.\u00a0<\/em>2024<\/strong>, 26<\/em>, 11722\u201311727. DOI<\/a><\/li>\r\n \t
      306. Hydrofluoroether Synthesis through One-Pot Anodic Iodoalkoxylation of Alkenes\r\nM. Becerra-Ruiz, B. Winterson, E. G. P\u00e9rez, T. Wirth,\u00a0Adv. Synth. Catal.\u00a0<\/em>2024<\/strong>, 367<\/em>, e202401108.\u00a0<\/em>DOI<\/a><\/li>\r\n \t
      307. B(C6<\/small>F5<\/small>)3<\/small> Catalyzed Regiodivergent Thioetherifications of Alkenes via Thiiranium Intermediates: Experimental and Computational Insights\r\nN. Alotaibi, R. Babaahmadi, S. Das, E. Richards, M. Pramanik, T. Wirth, R. L. Melen, Chem. Eur. J. <\/em>2024<\/strong>, 31<\/i>, e202404236. DOI<\/a><\/li>\r\n \t
      308. Raman Study of Intermediates Formed During the Electrochemical N<\/em>-Nitrosation of Secondary Amines\r\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><\/li>\r\n \t
      309. Synthesis and Reactivity of Six-Membered Cyclic Diaryl \u03bb3<\/small>-Bromanes and \u03bb3<\/small>-Chloranes\r\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>\r\nSynthese und Reaktivit\u00e4t sechsgliedriger zyklischer Diaryl<\/span> \u03bb3<\/small><\/span>–<\/span>Bromane und<\/span> \u03bb3-<\/small><\/span>Chlorane<\/span>\r\n<\/span><\/strong>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.<\/span>\u00a0DOI<\/a><\/li>\r\n \t
      310. Electrochemical Fluorination of Proline Derivatives\r\nP. Ryan, D. Bhattacherjee, T. Wirth, L. Hunter, G. Pascali,\u00a0Eur. J. Org. Chem.<\/em>\u00a02025<\/strong>, 28<\/em>, e202500264. DOI<\/a><\/li>\r\n \t
      311. Electrolyte-Controlled Regiodivergent Continuous FlowElectroselenocyclisations\r\nS. Arepally, H. Gieman, T. Wirth<\/span>, Angew. <\/em>Chem. Int. Ed. <\/em>2025<\/strong>, 64<\/em>, e202509811. DOI<\/a>\r\nElektrolytgesteuerte, regiodivergente, kontinuierliche Elektroselenozyklisierungen\r\n<\/span>\u00a0S. Arepally, H. Gieman, T. Wirth, <\/span>Angew. <\/em><\/span>Chem. <\/em><\/span>2025<\/strong>, 137<\/em>, e202509811.<\/i><\/span>\u00a0DOI<\/a><\/li>\r\n \t
      312. Flow electrochemical oxidation of N<\/i>-nitrosamines to N<\/i>-nitramines\r\nR. Ali, K. Matsui, J. \u0160adauskis, A. Catherall, T. Wirth, Chem. Commun. <\/em>2025<\/strong>, 61`<\/em>, 13671\u201313674.\u00a0DOI<\/a><\/li>\r\n \t
      313. Imidazopyridine substituted cyclic selenonium(IV) salts as chalcogen bond catalyst\r\nT. Kuzmera, P. Puylaert, T. Wirth, B. J. Nachtsheim, Chem. Commun. <\/em>2025<\/strong>, 61<\/em>, 14169\u201314172.\u00a0DOI<\/a><\/li>\r\n \t
      314. Electrochemical \u237a-C\u2013H Functionalization of Nitramines for Accessing Bifunctional Energetic Heterocycles\r\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><\/li>\r\n \t
      315. Electric-Field-Assisted Organic Synthesis: A New Frontier in Reactivity Control\r\nH. Chadwick, G. Cocking, J. Westph\u00e4ling, R. L. Melen, T. Wirth, SynOpen <\/em>2025<\/strong>, 9<\/em>, 282\u2013291. DOI<\/a><\/li>\r\n \t
      316. Oxidative Rearrangement of Alkynes to chiral \u03b1-Arylalkanoic Esters\r\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><\/li>\r\n \t
      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\r\nM. 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><\/li>\r\n \t
      318. Revealing the Mechanism of TEMPO-Hypervalent Iodine(III) Oxidation of Alcohols\r\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>\r\n<\/strong><\/li>\r\n \t
      319. Electrochemical Regioselective Chalcogenocyclizations of 2-Alkynylbenzamides in Flow\r\nH. Gieman,\u00a0S. Arepally,\u00a0T. Wirth,\u00a0ChemElectroChem<\/em>\u00a02026<\/strong>, 13<\/em>, e202500471. DOI<\/a><\/span><\/li>\r\n \t
      320. Synthesis and Structure of Group 13 POCOP Complexes\r\nS. Pahar, T. Wilde, K. Agrawal, N. T. Coles, B. M. Kariuki, D. L. Kays, A. J. Logsdail, T. Wirth, E. Richards, R. L. Melen, <\/span>Inorg. Chem.<\/em> 2026<\/strong>, 65<\/em>, 8289\u20138300<\/span>. <\/span>DOI<\/a><\/li>\r\n \t
      321. Borane Catalysed Annulative Sulfenylation of Internal Alkynes: Towards the Synthesis and Study of Highly Unsaturated Heterocycles\r\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. DOI<\/a><\/li>\r\n \t
      322. Numbering-Up Flow Electroreduction of \u03b1,\u03b2-Unsaturated Carbonyls from Gram to Pilot-Relevant Scale\r\nT. Boruah, S. Arepally, R. L. Melen, T. Wirth,\u00a0Org. Process Res. Dev. <\/em>2026<\/strong>, 30<\/em>, 2067\u20132074<\/span>. <\/em>DOI<\/a><\/span><\/li>\r\n \t
      323. Hydrogen bonding interactions in HFIP enabling the cascade synthesis of sulfenylated 2H<\/em>-chromenes\r\nD. H.-P. Mak, S. Das, J. Westph\u00e4ling, T. Jeans, A. Gorecka, T. Wirth, M. Pramanik, M.-H. Baik, R. L. Melen, Chem. Commun. <\/em>2026<\/strong>, 62<\/em>, 14821\u201314825.\u00a0DOI<\/a><\/li>\r\n \t
      324. Oxidative Flow Electrochemistry: A Platform for Generating Reactive Intermediates and Reaction Control\r\nS. Arepally, T. Boruah, R. L. Melen, T. Wirth,\u00a0Acc. Chem. Res.<\/em> 2026<\/strong>, 59,<\/em>\u00a02800\u20132815<\/span>. <\/em>DOI<\/a><\/li>\r\n \t
      325. Continuous Flow Electrochemical Oxidation of Activated Methylarenes Using O2\r\n<\/small><\/span>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><\/li>\r\n \t
      326. Condensing the Cage: Novel Insights into the Reaction Pathway of Isowurtzitane Cage Formation\r\nC. S. Wolfe, P. F. N. Stewart, R. M. Campbell, J. R. White, A. M. Beardah, J. Fellows, T. Wirth, Propellants Explos. Pyrotech. <\/em>2026<\/strong>,\u00a0in press. <\/em>DOI<\/a><\/span><\/small><\/span><\/li>\r\n<\/ol>\r\n<\/li>\r\n<\/ol>\r\n<\/li>\r\n<\/ol>","protected":false},"excerpt":{"rendered":"

        “Nucleophilic Additions to Acceptor-Substituted 2-Vinylindoles” S. Blechert, T. Wirth, Tetrahedron Lett. 1991, 32, 7237 – 7240. “Proton-induced Diels-Alder Reactions of 2-Vinylindoles” S. Blechert, T. Wirth, Tetrahedron Lett. 1992, 33, 6621 – 6624. “Synthesis of 2,3-Disubstituted Indoles” T. Wirth, S. Blechert, Synlett 1994, 717 – 718. “Direct Asymmetric alpha-Alkylation of Phenylalanine Derivatives Using No External Chiral […]<\/p>\n","protected":false},"author":474,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"open","template":"","meta":{"footnotes":""},"class_list":["post-45","page","type-page","status-publish","hentry"],"jetpack_sharing_enabled":true,"jetpack_shortlink":"https:\/\/wp.me\/P4Odwu-J","meta_box":[],"_links":{"self":[{"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/pages\/45","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\/474"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/comments?post=45"}],"version-history":[{"count":374,"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/pages\/45\/revisions"}],"predecessor-version":[{"id":2069,"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/pages\/45\/revisions\/2069"}],"wp:attachment":[{"href":"https:\/\/blogs.cardiff.ac.uk\/wirth\/wp-json\/wp\/v2\/media?parent=45"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}