Publications (all)

  1. “Nucleophilic Additions to Acceptor-Substituted 2-Vinylindoles”
    S. Blechert, T. Wirth, Tetrahedron Lett. 1991, 32, 7237 – 7240.
  2. “Proton-induced Diels-Alder Reactions of 2-Vinylindoles”
    S. Blechert, T. Wirth, Tetrahedron Lett. 1992, 33, 6621 – 6624.
  3. “Synthesis of 2,3-Disubstituted Indoles”
    T. Wirth, S. Blechert, Synlett 1994, 717 – 718.
  4. “Direct Asymmetric alpha-Alkylation of Phenylalanine Derivatives Using No External Chiral Source”
    T. Kawabata, T. Wirth, K. Yahiro, H. Suzuki, K.Fuji, J. Am. Chem. Soc. 1994, 116, 10809 – 10810.
  5. “Domino Reactions – New Concepts in the Synthesis of Indole Alkaloids and Other Polycyclic Indole Derivatives”
    S. Blechert, R. Knier, H. Schroers, T. Wirth, Synthesis 1995, 592 – 604.
  6. “Asymmetric Reaction of Arylalkenes with Diselenides”
    T. Wirth, Angew. Chem. 1995, 107, 1872 – 1873; Angew. Chem. Int. Ed. Engl. 1995, 34, 1726 – 1728.
  7. “Enantioselective Alkylation of Aldehydes Catalyzed by New Chiral Diselenides”
    T. Wirth, Tetrahedron Lett. 1995, 36, 7849 – 7852.
  8. “Memory of Chirality: Direct Asymmetric alpha-Alkylation of Phenylalanine Derivatives”
    T. Kawabata, T. Wirth, K. Yahiro, H. Suzuki, K.Fuji, ICR Ann. Rep. 1996, 3, 36 – 37.
  9. “‘New’ Reagents for the ‘Old’ Pinacol Coupling Reaction”
    T. Wirth, Angew. Chem. 1996, 108, 65 – 67; Angew. Chem. Int. Ed. Engl. 1996, 35, 61 – 63.
  10. “Vom Periodensystem zum genetischen Code” (book review)
    T. Wirth, Nachr. Chem. Tech. Lab. 1996, 44, 407 – 408.
  11. “Chiral Diselenides in the Total Synthesis of (+)-Samin”
    T. Wirth, K. J. Kulicke, G. Fragale, J. Org. Chem. 1996, 61, 2686 – 2689.
  12. “Chiral Diselenides from Benzylamines as Catalysts in the Diethylzinc Addition to Aldehydes”
    T. Wirth, K. J. Kulicke, G. Fragale, Helv. Chim. Acta 1996, 79, 1957 – 1966.
  13. “Bioorganische Chemie” (conference report)
    M. Kalesse, T. Wirth, Nachr. Chem. Tech. Lab.1996 , 44, 1178 – 1181.
  14. “Chiral Hypervalent Iodine Compounds”
    T. Wirth, U. H. Hirt, Tetrahedron: Asymmetry 1997, 8, 23 – 26.
  15. “New Strategies to alpha-Alkylated alpha-Aminoacids”
    T. Wirth, Angew. Chem. 1997, 109, 235 – 237; Angew. Chem. Int. Ed. Engl. 1997, 36, 225 – 227.
  16. “Trendbericht 1996: Metallorganische Chemie” (review)
    T. Wirth, Nachr. Chem. Tech. Lab. 1997, 45, 148 – 152.
  17. “First Total Synthesis of (+)-Membrine”
    T. Wirth, Liebigs Ann./Recueil 1997, 1155 – 1158.
  18. “Vom Mond zur Erde: vom Selen zum Tellur” (conference report)
    T. Wirth, Nachr. Chem. Tech. Lab. 1997, 45, 987.
  19. “Asymmetric Addition Reactions with Optimized Selenium Electrophiles”
    T. Wirth, G. Fragale, Chem. Eur. J. 1997, 3, 1894 – 1902.
  20. “Chiral Selenium Compounds: Versatile Reagents in Organic Synthesis”
    T. Wirth, Liebigs Ann./Recueil 1997, 2189 – 2196.
  21. “Syntheseplanung – aber wie?” (book)
    T. Wirth, Spektrum Akademischer Verlag, Heidelberg 1998, 206 pages.
  22. “Stereoselective Isoquinoline Alkaloid Synthesis with New Diselenides”
    T. Wirth, G. Fragale, Synthesis 1998, 162 – 166.
  23. “‘New’ Reagents for the ‘Old’ Pinacol Coupling Reaction” (book chapter)
    T. Wirth in Organic Synthesis Highlights III, Eds.: H. Waldmann, J. Mulzer, VCH, Weinheim 1998, 113 – 118.
  24. “Catalytic Asymmetric Oxyselenenylation – Elimination Reactions using Chiral Selenium Compounds”
    T. Wirth, S. Häuptli, M. Leuenberger, Tetrahedron: Asymmetry 1998, 9, 547 – 550.
  25. “Mechanistic Course of the Asymmetric Methoxyselenenylation Reaction”
    T. Wirth, G. Fragale, M. Spichty, J. Am. Chem. Soc. 1998, 120, 3376 – 3381.
  26. “Chiral Diselenides in Asymmetric Cyclization Reactions”
    G. Fragale, T. Wirth, Eur. J. Org. Chem. 1998, 1361 – 1369.
  27. “Glutathione Peroxidase-like Activities of Oxygen-Containing Diselenides”
    T. Wirth, Molecules 1998, 3, 164 – 166.
  28. “Stereoselection at the Steady State: The Design of New Asymmetric Reactions”
    T. Wirth, Angew. Chem. 1998, 110, 2179 – 2181; Angew. Chem. Int. Ed. Engl. 1998, 37, 2069 – 2071.
  29. “New and Efficient Selenium Reagents for Stereoselective Selenenylation Reactions”
    G. Fragale, T. Wirth, Chem. Commun. 1998, 1867 – 1868.
  30. “New Chiral Hypervalent Iodine Compunds in Asymmetric Synthesis”
    U. H. Hirt, B. Spingler, T. Wirth, J. Org. Chem. 1998, 63, 7674 – 7679. DOI
  31. “Synthesis of a New Chiral Nitrogen Containing Diselenide as a Precursor for Selenium Electrophiles”
    C. Santi, G. Fragale, T. Wirth, Tetrahedron: Asymmetry 1998, 9, 3625 – 3628.
  32. “Asymmetric Synthesis with Chiral Diselenides”
    T. Wirth, Phosphorus Sulfur 1998, 136, 235 – 238.
  33. “Chiral Selenium Compounds in Organic Synthesis”
    T. Wirth, Tetrahedron 1999, 55, 1 – 28.
  34. “Synthesis of Non Racemic Nitrogen Containing Diselenides as Efficient Precursor Catalysts in the Diethylzinc Addition to Benzaldehyde”
    C. Santi, T. Wirth, Tetrahedron: Asymmetry 1999, 10, 1019 – 1023.
  35. “Stereoselective Oxidation Reactions”
    T. Wirth, Chimia 1999, 53, 230 – 231.
  36. “Hypervalent Iodine Compounds: Recent Advances in Synthetic Applications” (review)
    T. Wirth, U. H. Hirt, Synthesis 1999, 1271 – 1287.
  37. “The Origin of Stereoselectivities in Asymmetric Alkoxyselenenylations”
    X. Wang, K. N. Houk, M. Spichty, T. Wirth, J. Am. Chem. Soc. 1999, 121, 8567 – 8576.
  38. “Selenium Compounds in Chemical and Biological Oxidation Reactions”
    G. Fragale, S. Häuptli, M. Leuenberger, T. Wirth in New Aspects in Bioorganic Chemistry, Eds.: U. Diederichsen, T. K. Lindhorst, L. Wessjohann, B. Westermann, VCH, Weinheim, 1999, 48 – 52.
  39. “Organoselenium Chemistry: Modern Developments in Organic Synthesis”
    Top. Curr. Chem., Ed.: T. Wirth, 2000, 208.
  40. “Introduction and General Aspects”
    T. Wirth, Top. Curr. Chem. 2000, 208, 1 – 5.
  41. “New Strategies to alpha-Alkylated alpha-Aminoacids” (book chapter)
    T. Wirth in Organic Synthesis Highlights IV, Ed.: H.-G. Schmalz, VCH, Weinheim, 2000, 26 – 33.
  42. “Stereoselection at the Steady State: The Design of New Asymmetric Reactions” (book chapter)
    T. Wirth in Organic Synthesis Highlights IV, Ed.: H.-G. Schmalz, VCH, Weinheim, 2000, 67 – 70.
  43. “Oxygen and Osmium – A New Alliance for Dihydroxylations?” (Highlight)
    T. Wirth, Angew. Chem. 2000, 112, 342 – 343; Angew. Chem. Int. Ed. Engl. 2000, 39, 334 – 335.
  44. Organoselenium Chemistry (book review)
    T. Wirth, Angew. Chem. 2000, 112, 3859 – 3860, Angew. Chem. Int. Ed. 2000, 39, 1515.
  45. “Tagungen im Netz: Zukunft oder Spielerei?”
    T. Wirth, Nachr. Chem. 2000, 48, 925.
  46. “Organoselenium Chemistry in Stereoselective Synthesis”
    T. Wirth, Angew. Chem. 2000, 112, 3890 – 3900, Angew. Chem. Int. Ed. 2000, 39 , 3742 – 3751.
  47. “Theoretical Investigations on the Stereoselective Selenenylation Reaction of Alkenes”
    M. Spichty, G. Fragale, T. Wirth, J. Am. Chem. Soc. 2000, 122, 10914 – 10916.
  48. “Chiral Selenium Electrophiles on Solid-Support”
    L. Uehlin, T. Wirth, Chimia 2001, 55, 65 – 67.
  49. “Chiral Hypervalent Organo-Iodine(III) Compounds”
    U. H. Hirt, M. F. H. Schuster, A. N. French, O. G. Wiest, T. Wirth, Eur. J. Org. Chem. 2001, 1569 – 1579.
  50. “Novel Polymer-Bound Chiral Selenium-Electrophiles”
    L. Uehlin, T. Wirth, Org. Lett. 2001, 3, 2931 – 2933.
  51. “Mixed Acetals as New Precursors for Selenium Electrophiles”
    L. Uehlin, T. Wirth, Phosphorus Sulfur 2001, 172, 189 – 194.
  52. “IBX – New Reactions with an Old Reagent” (highlight)
    T. Wirth, Angew. Chem. 2001, 113, 2893 – 2895, Angew. Chem. Int. Ed. 2001, 40, 2812 – 2814.
  53. “Hypervalentes Iod” (conference report)
    T. Wirth, Nachr. Chem. 2001, 49, 1450.
  54. “Reagent-Controlled Stereoselective Halolactonizations”
    J. Haas, S. Piguel, T. Wirth, Org. Lett. 2002, 4, 297 – 300.
  55. “New and Efficient Chiral Selenium Electrophiles”
    L. Uehlin, G. Fragale, T. Wirth, Chem. Eur. J. 2002, 8, 1125 – 1133.
  56. A cellular model for Friedreich Ataxia reveals an impaired selenium homeostasis that can be overcome by small-molecule GPX-mimetics
    M. Jauslin, T. Wirth, T. Meier, F. Schoumacher, Hum. Mol. Gen. 2002, 11, 3055 – 3063.
  57. “Hypervalent Iodine Compounds” (book)
    Top. Curr. Chem. Ed.: T. Wirth, 2003, 224.
  58. “Introduction and General Aspects” (book chapter)
    T. Wirth, Top. Curr. Chem. 2003, 224, 1 – 4.
  59. “Oxidations and Rearrangements” (book chapter)
    T. Wirth, Top. Curr. Chem. 2003, 224, 185 – 208.
  60. “Organic Synthesis Highlights V” (book)
    Eds.: H.-G. Schmalz, T. Wirth, VCH, Weinheim, 2003. online book
  61. “IBX – New Reactions with an Old Reagent” (book chapter)
    T. Wirth in “Organic Synthesis Highlights V“, Eds.: H.-G. Schmalz, T. Wirth, VCH, Weinheim, 2003, 144 – 150.
  62. “Novel Lactonization with Phenonium Ion Participation Induced by Hypervalent Iodine Reagents”
    A. C. Boye, D. Meyer, C. K. Ingison, A. N. French, T. Wirth, Org. Lett. 2003, 5, 2157-2159. DOI
  63. “Cyclopropanation of Alkenes using Hypervalent Iodine Reagents”
    A. S. Biland, S. Altermann, T. Wirth, ARKIVOC 2003, 6, 164-169.
  64. “Direct Iodination of Alkanes”
    R. Montoro, T. Wirth, Org. Lett. 2003, 5, 4729-4731.
  65. “Selenocyclizations: Control by Coordination and by the Counterion”
    S. S. Khokhar, T. Wirth, Angew. Chem. Int. Ed. 2004, 43, 631 – 633.
  66. “Iodine Electrophiles in Stereoselective Reactions: Recent Developments and Synthetic Applications”
    A. N. French, S. Bissmire, T. Wirth, Chem. Soc. Rev. 2004, 33, 354-362.
  67. “Tetrahydrofuranylation of Alcohols using Hypervalent Iodine Reagents”
    A. N. French, J. Cole, T. Wirth, Synlett 2004, 2291-2293.
  68. “Nucleophile-selective Selenocyclizations”
    S. S. Khokhar, T. Wirth, Eur. J. Org. Chem. 2004, 4567-4581.
  69. “Fluorinations of alpha-Seleno Carboxylic Acid Derivatives with Hypervalent (Difluoroiodo)toluene”
    M. A. Arrica, T. Wirth, Eur. J. Org. Chem. 2005, 395-403.
  70. “Solvent-free Reactions with Hypervalent Iodine Reagents”
    M. S. Yusubov, T. Wirth, Org. Lett. 2005, 7, 519-521.
  71. “Synthesis of a Selenium-Substituted Diselenide”
    M. Cox, T. Wirth,Phosphorus Sulfur 2005, 180, 659-666.
  72. “Direct Bromination and Iodination of Non-activated Alkanes by Hypohalite Reagents”
    R. Montoro, T. Wirth, Synthesis 2005, 1473-1478.
  73. “Selenocarboxylic Acids and Derivatives” (book chapter)
    T. Wirth in Science of Synthesis, Vol. 22, Ed. A. Charette, Thieme, Stuttgart, 2005, 181-212.
  74. “Hypervalent Iodine Chemistry in Synthesis: Scope and New Directions”
    T. Wirth, Angew. Chem. 2005, 117, 3722-3731; Angew. Chem. Int. Ed. 2005, 44, 3656-3665.
  75. “Iodine Monochloride – Amine Complexes: An Experimental and Computational Approch to New Chiral Electrophiles”
    J. Haas, S. Bissmire, T. Wirth, Chem. Eur. J. 2005, 11, 5777-5785.
  76. “Electrochemical Generation and Catalytic Use of Selenium Electrophiles”
    O. Niyomura, M. Cox, T. Wirth, Synlett 2006, 251-254.
  77. “Enhancement of Reaction Rates by Segmented Fluid Flow in Capillary Scale Reactors”
    B. Ahmed, D. Barrow, T. Wirth, Adv. Synth. Catal. 2006, 348, 1043-1048.
  78. “Hypervalent Iodine goes Catalytic”
    R. D. Richardson, T. Wirth, Angew. Chem. 2006, 118, 4510-4512; Angew. Chem. Int. Ed. 2006, 45, 4402-4404.
  79. “(S,S)-Bis[2-(1-hydroxypropyl)phenyl] diselenide”
    T. Wirth in Electronic Encyclopedia of Reagents for Organic Synthesis, Ed. L. A. Paquette, John Wiley & Sons, 2006 DOI
  80. “Simple Direct Synthesis of [Bis(trifluoroacetoxy)iodo]arenes”
    T. K. Page, T. Wirth, Synthesis 2006, 3153-3155.
  81. “Selenium”
    T. Wirth in Comprehensive Organometallic Chemistry III (COMC-3), Eds.: R. H. Crabtree, D. M. P. Mingos, P. Knochel, Elsevier, London, Vol. 9, 457-500.
  82. “New Developments with Chiral Electrophilic Selenium Reagents”
    D. M. Browne, T. Wirth, Curr. Org. Chem. 2006, 10, 1893-1903.
  83. “Stereoselective Addition Reactions with Chalcogen Electrophiles”
    F. W. Bürgler, G. Fragale, T. Wirth, ARKIVOC 2007, 21-28. PDF
  84. “Enantioselective ?-Oxytosylation of Ketones Catalysed by Iodoarenes”
    R. D. Richardson, T. K. Page, S. Altermann, S. M. Paradine, A. N. French, T. Wirth, Synlett 2007, 538-542. DOI
  85. “Advanced Organic Synthesis using Microreactor Technology”
    B. Ahmed, J. C. Brandt, T. Wirth, Org. Biomol. Chem. 2007, 5, 733-740. DOI
  86. “Hypervalent Iodine-Mediated Aziridination of Alkenes: Mechanistic Insights and Requirements for Catalysis”
    R. D. Richardson, M. Desaize, T. Wirth, Chem. Eur. J. 2007, 13, 6745-6754. DOI
  87. “Tetrafluoro IBA and IBX: New Hypervalent Iodine Reagents”
    R. D. Richardson, J. M. Zayed, S. Altermann, D. Smith, T. Wirth, Angew. Chem. Int. Ed. 2007, 46, 6649-6652. DOI Featured in SYNFORM
  88. “Catalytic Use of Selenium Electrophiles in Cyclizations”
    D. M. Browne, O. Niyomura, T. Wirth, Org. Lett. 2007, 9, 3169-3171. DOI
  89. “Cyclic Alkanesulfenic Acid Derivatives”
    T. Wirth, Science of Synthesis Vol. 39, 2007, 879-884.
  90. “Alkaneselenenic Acids and Acyclic Derivatives”
    T. Wirth, Science of Synthesis Vol. 39, 2007, 1005-1012.
  91. “Cyclic Alkaneselenenic Acid Derivatives”
    T. Wirth, Science of Synthesis Vol. 39, 2007, 1093-1096.
  92. “Alkanetelluric Acids and Acyclic Derivatives”
    T. Wirth, Science of Synthesis Vol. 39, 2007, 1193-1196.
  93. Cyclic Alkanetelluric Acids Derivatives”
    T. Wirth, Science of Synthesis Vol. 39, 2007, 1243-1244.
  94. “Effect of Segmented Fluid Flow, Sonication and Phase Transfer Catalysis on Biphasic Reactions in Capillary Microreactors”
    B. Ahmed-Omer, D. Barrow, T. Wirth, Chem. Eng. J. 2008, 135S, S280-S283. DOI
  95. “Microreactors in Organic Chemistry and Catalysis” (book)
    Ed.: T. Wirth, Wiley-VCH, 2008.
  96. “Liquid – Liquid Biphasic Reactions” (book chapter)
    B. Ahmed-Omer, T. Wirth in Microreactors in Organic Chemistry and Catalysis, Ed.: T. Wirth, Wiley-VCH, Weinheim, 2008, 122-139.
  97. “Catalytic addition-elimination reactions towards butenolides”
    D. M. Browne, O. Niyomura, T. Wirth, Phosphorus Sulfur 2008, 183, 1026-1035. DOI
  98. “Tetraazafulvalene: Organisches Natrium”
    R. D. Richardson, T. Wirth, Chem. unserer Zeit 2008, 42, 190-191. DOI
  99. “Diisobutylaluminium Phenyl Selenide”
    Z. A. Khan, T. Wirth in Electronic Encyclopedia of Reagents for Organic Synthesis, Ed. L. A. Paquette, John Wiley & Sons, 2008. DOI
  100. “Dimethyl Selenoxide”
    Z. A. Khan, T. Wirth in Electronic Encyclopedia of Reagents for Organic Synthesis, Ed. L. A. Paquette, John Wiley & Sons, 2008. DOI
  101. “Catalytic Enantioselective α-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. 2008, 5315-5328. DOI
  102. “Dimethylaluminum Methylselenolate”
    S. A. Shahzad, T. Wirth in Electronic Encyclopedia of Reagents for Organic Synthesis, Ed. L. A. Paquette, John Wiley & Sons, 2009, DOI
  103. “Diphenylselenium Bis(trifluoroacetate)”
    S. A. Shahzad, T. Wirth in Electronic Encyclopedia of Reagents for Organic Synthesis, Ed. L. A. Paquette, John Wiley & Sons, 2008, DOI
  104. “tert-Butyl Hypoiodite”
    T. Wirth in Electronic Encyclopedia of Reagents for Organic Synthesis, Ed. L. A. Paquette, John Wiley & Sons, 2008, DOI
  105. “Hypervalent Iodine Reagents: Synthesis and Catalysis”
    T. Wirth, SIS Report No. 11, 2008, 116-123.
  106. “Synthesis of Indene Derivatives via Electrophilic Cyclization”
    Z. A. Khan, T. Wirth, Org. Lett. 2009, 11, 229-231. DOI
  107. “Recent Developments in Carbocation and Onium Chemistry” (book review)
    T. Wirth, Angew. Chem. 2009, 121, 443; Angew. Chem. Int. Ed. 2009, 48, 435. DOI
  108. “Hypervalent Bromine Compounds: Smaller, More Reactive Analogues of Hypervalent Iodine Compounds”
    U. Farooq, A. A. Shah, T. Wirth, Angew. Chem. 2009, 121, 1036-1038; Angew. Chem. Int. Ed. 2009, 48, 1018-1020. DOI
  109. “Fast Synthesis of Benzofluorenes by Selenium Mediated Carbocyclizations”
    S. A. Shahzad, T. Wirth, Angew. Chem. 2009, 121, 2626-2628; Angew. Chem. Int. Ed. 2009, 48, 2588-2591. DOI
  110. “Recent Advances in Organoselenium Chemistry”
    D. M. Freudendahl, S. A. Shahzad, T. Wirth, Eur. J. Org. Chem. 2009, 1649-1664. DOI
  111. “Heck Reactions using Segmented Flow Conditions”
    B. Ahmed-Omer, D. A. Barrow, T. Wirth, Tetrahedron Lett. 2009, 50, 3352-3355. DOI
  112. “Synthesis of Chiral Acetals by Asymmetric Selenenylations”
    L. Uehlin, T. Wirth, Phosphorus Sulfur 2009, 184, 1374-1385. DOI
  113. “Controlling Hazardous Chemicals in Microreactors: Synthesis with Iodine Azide”
    J. C. Brandt, T. Wirth, Beilstein J. Org. Chem. 2009, 5, No. 30. DOI
  114. “Iodoxolone-Based Hypervalent Iodine Reagents”
    A. A. Shah, Z. A. Khan, N. Choudhary, C. Lohölter, S. Schäfer, G. P. L. Marie, U. Farooq, B. Witulski, T. Wirth, Org. Lett. 2009, 11, 3578-3581. DOI
  115. “Homogeneous Catalysis using Microreactor Technology”
    J. C. Brandt, T. Wirth, in Recoverable and Recyclable Catalysts, Ed.: M. Benaglia, John Wiley & Sons, 2009, 411-425.
  116. “Classics in Stereoselective Synthesis” (book review)
    T. Wirth, Chemistryworld, November 2009, 63.
  117. “Green Chemistry with Selenium Reagents: Development of Efficient Catalytic Reactions”
    D. M. Freudendahl, S. Santoro, S. A. Shahzad, C. Santi, T. Wirth, Angew. Chem. 2009, 121, 8559-8562; Angew. Chem. Int. Ed. 2009, 48, 8409-8411. DOI
  118. “Authorprofile: Thomas Wirth”
    Angew. Chem. 2010, 122, 1570; DOI Angew. Chem. Int. Ed. 2010, 49, 1528. DOI
  119. “Synthesis of new Enantiomerically pure Organoiodine Catalysts and their Application in the α-Functionalization of Ketones”
    U. Farooq, S. Schäfer, A. A. Shah, D. M. Freudendahl, T. Wirth, Synthesis 2010, 1023-1029. DOI
  120. “Selenium-Mediated Synthesis of Biaryls through Rearrangement”
    S. A. Shahzad, C. Vivant, T. Wirth, Org. Lett. 2010, 12, 1364-1367. DOI
  121. “A New Versatile and Highly Reactive Polyfluorinated Hypervalent Iodine(III) Compound”
    S. Schäfer, T. Wirth, Angew. Chem. 2010, 122, 2846-2850; DOI Angew. Chem. Int. Ed. 2010, 49, 2786-2789. DOI
  122. “Diselenide- and Disulfide-Mediated Synthesis of Isocoumarins”
    S. A. Shahzad, C. Venin, T. Wirth, Eur. J. Org. Chem. 2010, 3465-3472. DOI
  123. “Synthesis of New Sulfoxide-Containing Diselenides and Unexpected Cyclization Reactions to 2,3-Dihydro-1,4-benzoselenothiine 1-Oxides”
    D. M. Freudendahl, M. Iwaoka, T. Wirth, Eur. J. Org. Chem. 2010, 3934-3944. DOI
  124. “Triptycene Derivatives: Synthesis and Applications”
    L. Zhao, Z. Li, T. Wirth, Chem. Lett. 2010, 39, 658-667. DOI
  125. “Hypervalent Iodine Chemistry – Recent Advances and Applications”
    S. Quideaux, T. Wirth, Tetrahedron 2010, 66, 5737-5738. DOI
  126. “New Chiral Hypervalent Iodine(V) Compounds as Stoichiometric Oxidants”
    S. M. Altermann, S. Schäfer, T. Wirth, Tetrahedron 2010, 66, 5902-5907. DOI
  127. “Novel Cyclization Cascades to Functionalized Indanes and Tetrahydronaphthalenes”
    Z. A. Khan, M. Iwaoka, T. Wirth, Tetrahedron 2010, 66, 6639-6646. DOI
  128. “Molecular imprinted polymers binding low functionality templates”
    Y. Luk, C. J. Allender, T. Wirth, Tetrahedron Lett. 2010, 51, 5883-5885. DOI
  129. “Safe and Efficient Ritter Reactions in Flow”
    J. C. Brandt, S. C. Elmore, R. I. Robinson, T. Wirth, Synlett 2010, 3099-3103. DOI
  130. “Preparation of Novel Chiral Non-Racemic Diselenides and Applications in Asymmetric Synthesis”
    L. Zhao, Z. Li, T. Wirth, Eur. J. Org. Chem. 2011, 176-182. DOI
  131. “Siegfried Blechert: A Tribute”
    T. Wirth, Arkivoc 2011, (iv), 1 – 5. PDF
  132. “Intelligent Microflow: Development of Self-Optimizing Reaction Systems”
    M. Rasheed, T. Wirth, Angew. Chem. 2011, 123, 374-376. DOI Angew. Chem. Int. Ed. 2011, 50, 357-358. DOI
  133. “Multistep reactions using microreactor chemistry”
    B. Ahmed-Omer, D. A. Barrow, T. Wirth, Arkivoc 2011, (iv), 26-36. PDF
  134. “Asymmetric reactions in flow reactors”
    M. Rasheed, S. C. Elmore, T. Wirth, in Catalytic Methods in Asymmetric Synthesis, Eds.: M. Gruttadauria, F. Giacalone, John Wiley & Sons, 2011, 345-371.
  135. “Fast optimisation of a Diels-Alder reaction in a flow microreactor by in-line HPLC analysis”
    M. Rasheed, T. Wirth, Chem. Today 2011, 29, 54-56. INFO
  136. “A practical microreactor for electrochemistry in flow”
    K. Watts, W. Gattrell, T. Wirth, Beilstein J. Org. Chem. 2011, 7, 1108-1114. PDF
  137. “New Selenium Electrophiles and Their Reactivity”
    D. M. Freudendahl, T. Wirth, in Selenium and Tellurium Chemistry, Eds.: J. D. Woolins, R. S. Laitinen, Springer, 2011, 41-55. INFO PDF
  138. “Asymmetric Methoxyselenenylations with Novel Chiral Selenium Electrophiles”
    L. Zhao, Z. Li, T. Wirth, Eur. J. Org. Chem. 2011, 7080-7082. DOI
  139. “Organoselenium Chemistry”
    Ed. T. Wirth, Wiley-VCH, 2011 Book at WILEY-VCH
  140. “Selenium Compounds as Ligands and Catalysts”
    F. V. Singh, T. Wirth, in Organoselenium Chemistry Ed.: T. Wirth, Wiley-VCH, 2011 321-360.
  141. “Selenium-catalyzed Regioselective Cyclization of Unsaturated Carboxylic Acids Using Hypervalent Iodine Oxidants”
    F. V. Singh, T. Wirth, Org. Lett., 2011, 13, 6504-6507. DOI
  142. Ritter Reactions in Flow
    L. Audiger, K. Watts, S. C. Elmore, R. I. Robinson, T. Wirth, ChemSusChem 2012, 5, 257-260. DOI
  143. Flow Chemistry: Enabling Technology in Drug Discovery and Process Research
    T. Wirth, ChemSusChem 2012, 5, 215-216. DOI
  144. Opening up the World of Chemistry
    R. Martínez-Máñez, T. Wirth, ChemistryOpen 2012, 1, 4. DOI
  145. Highly Stereoselective Metal-Free Oxyaminations Using Chiral Hypervalent Iodine Reagents
    U. Farid, T. Wirth, Angew. Chem. 2012, 124, 3518-3522; DOI Angew. Chem. Int. Ed., 2012, 51, 3462-3465. DOI
  146. Stereoselective reactions of organoselenium reagents including catalysis
    F. V. Singh, T. Wirth, in Patai Series: Organic Selenium and Tellurium Compounds, Vol. 3, Ed.: Z. Rappoport, John Wiley & Sons, 2012, 303-355. DOI
  147. Selenium-containing Naphthalimides as Anticancer Agents: Design, Synthesis and Bioactivity
    L. Zhao, J. Li, Y. Li, J. Liu, T. Wirth, Z. Li, Bioorg. Med. Chem. 2012, 20, 2558-2563. DOI
  148. Hypervalent Iodine Mediated Oxidative Cyclization of o-Hydroxystilbenes into Benzo- and Naphthofurans
    F. V. Singh, T. Wirth, Synthesis 2012, 44, 1171-1177. DOI
  149. Selenenylations of alkenes with styrene nucleophiles
    E. Gabriele, F. V. Singh, D. M. Freudendahl, T. Wirth, Tetrahedron 2012, 68, 10573-10576. DOI
  150. Stereoselective selenium catalyzed dihydroxylation and hydroxymethoxylation of alkenes
    C. Santi, R. Di Lorenzo, C. Tidei, L. Bagnoli, T. Wirth, Tetrahedron 2012, 68, 10530–10535. DOI
  151. 5,6,7,8-Tetrafluoro-1-hydroxy-1-oxobenziodoxol-3(1H)one (Tetrafluoro-IBX)
    U. Farid, T. Wirth, Encyclopedia of Reagents for Organic Synthesis [Online], John Wiley & Sons Ltd., 2012. DOI
  152. Facile Oxidative Rearrangements Using Hypervalent Iodine Reagents
    F. V. Singh, J. Rehbein, T. Wirth, ChemistryOpen 2012, 1, 245-250. DOI
  153. Stereoselective Reactions with Hypervalent Iodine Compounds
    U. Farid, T. Wirth, in Asymmetric Synthesis II, Eds.: M. Christmann, S. Bräse, Wiley VCH, 2012, 197 – 203. Wiley
  154. Hypervalent Iodine Reagents as Powerful Electrophiles
    M. Brown, U. Farid, T. Wirth, Synlett 2013, 24, 424-431. DOI
  155. Microreactors in Organic Synthesis and Catalysis – 2nd Edition
    Ed.: T. Wirth, Wiley-VCH, 2013. Wiley
  156. Liquid – Liquid Biphasic Reactions” (book chapter)
    M. J. Hutchings, B. Ahmed-Omer, T. Wirth in Microreactors in Organic Chemistry and Catalysis – 2nd Edition, Ed.: T. Wirth, Wiley-VCH, Weinheim, 2013, 197-219.
  157. Stereoselective Rearrangements with Chiral Hypervalent Iodine Reagents
    U. Farid, F. Malmedy, R. Claveau, L. Albers, T. Wirth, Angew. Chem. 2013, 125, 7156-7160; DOI Angew. Chem. Int. Ed. 2013, 52, 7018-7022. DOI
  158. Flow Chemistry in Undergraduate Organic Chemistry Education
    B. König, P. Kreitmeier, P. Hilgers, T. Wirth, J. Chem. Educ. 2013, 90, 934-936. DOI
  159. Hypervalent Iodine / TEMPO – mediated Oxidation in Flow Systems: A Fast and Efficient Protocol for Alcohol Oxidation
    N. Ambreen, R. Kumar, T. Wirth, Beilstein J. Org. Chem. 2013, 9, 1437-1442. DOI
  160. Flow Synthesis of Symmetrical Di- and Trisulfides using Phase-Transfer Catalysis
    A. Baker, M. Graz, R. Saunders, G. J. S. Evans, S. Kaul, T. Wirth, J. Flow Chem. 2013, 3, 118-121. DOI
  161. Current research on mimics and models of selenium-containing antioxidants
    B. J. Bhuyan, D. S. Lamani, G. Mugesh, T. Wirth, in Handbook of Chalcogen Chemistry, Eds.: F. A. Devillanova, W. W. du Mont, RSC, 2013, Vol. 2, 25-46. RSC
  162. Oxidative Rearrangements with Hypervalent Iodine Reagents
    F. V. Singh, T. Wirth, Synthesis 2013, 45, 2499-2511. DOI
  163. Efficient Terpene Synthase Catalysis by Extraction in Flow
    O. Cascón, G. Richter, R. K. Allemann, T. Wirth, ChemPlusChem 2013, 78, 1334-1337. DOI
  164. Difluoro- and Trifluoromethylation of Electron-deficient Alkenes in an Electrochemical Microreactor
    K. Arai, K. Watts, T. Wirth, ChemistryOpen 2014, 3, 23-28. DOI
  165. Hypervalent Iodine-Catalyzed Oxidative Functionalizations including Stereoselective Reactions
    F. V. Singh, T. Wirth, Chem. Asian J. 2014, 9, 950-971. DOI
  166. Electrochemical Synthesis in Microreactors
    K. Watts, A. Baker, T. Wirth, J. Flow Chem. 2014, 4, 2-11. DOI
  167. Safe Generation and Direct Use of Diazoesters in Flow Chemistry
    S. T. R. Müller, D. Smith, P. Hellier, T. Wirth, Synlett 2014, 25, 871-875. DOI Highlighted in Org. Process Res. Dev. 2014, 18, 840. Featured on the Organic Chemistry Portal
  168. Oxidative Functionalization with Hypervalent Halides
    F. V. Singh, T. Wirth, in: G. A. Molander, P. Knochel (eds.), Comprehensive Organic Synthesis, 2nd edition, Vol 7, Oxford: Elsevier; 2014, 880-933. DOI
  169. Flexible Stereoselective Functionalizations of Ketones through Umpolung with Hypervalent Iodine Reagents
    P. Mizar, T. Wirth, Angew. Chem. 2014, 126, 6103-6107; DOI Angew. Chem. Int. Ed., 2014, 53, 5993-5997. DOI
  170. Synthesis and Antioxidant Activities of Novel Chiral Ebselen Analogues
    M. Elsherbini, W. S. Hamama, H. H. Zoorob, D. Bhowmick, G. Mugesh, T. Wirth, Heteroatom Chem. 2014, 25, 320-325. DOI
  171. Enantioselective Diamination with Novel Chiral Hypervalent Iodine Catalysts
    P. Mizar, A. Laverny, M. El-Sherbini, U. Farid, M. Brown, F. Malmedy, T. Wirth, Chem. Eur. J. 2014, 20, 9910-9913. DOI
  172. Rapid Electrochemical Deprotection of the Isonicotinyloxycarbonyl Group from Carbonates and Thiocarbonates in a Microfluidic Reactor
    K. Arai, T. Wirth, Org. Process Res. Dev. 2014, 18, 1377-1381. DOI Featured on the Organic Chemistry Portal
  173. Organocatalytic Stereoselective Iodoamination of Alkenes
    P. Mizar, A. Burrelli, E. Günther, M. Söftje, U. Farooq, T. Wirth, Chem. Eur. J. 2014, 20, 13113–13116. DOI
  174. High-Temperature Synthesis of Amides from Alcohols or Aldehydes by Using Flow Chemistry
    N. Ambreen, T. Wirth, Eur. J. Org. Chem. 2014, 7590-7593. DOI
  175. Synthesis of Quinolinequinone Derivatives and related Carbocyclic Compounds
    S. A. Egu, U. C. Okoro, T. Wirth, ScienceOpen Research 2015 (DOI: 10.14293/S2199-1006.1.SOR-CHEM.AALL9P.v1) DOI
  176. Diazo compounds in continuous flow technology
    S. T. R. Müller, T. Wirth, ChemSusChem 2015, 8, 245-250. DOI
  177. Convenient Synthesis of Diaryliodonium Salts for the Production of [18F]F-DOPA
    R. Edwards, A. D. Westwell, S. Daniels, T. Wirth, Eur. J. Org. Chem. 2015, 625-630. DOI
  178. Rapid Generation and Safe Use of Carbenes Enabled by a Novel Flow Protocol with In-line IR spectroscopy
    S. T. R. Müller, A. Murat, D. Maillos, P. Lesimple, P. Hellier, T. Wirth, Chem. Eur. J. 2015, 21, 7016-7020. DOI Featured on the Organic Chemistry Portal
  179. [18F]6-fluoro-3,4-dihydroxy- l-phenylalanine – recent modern syntheses for an elusive radiotracer
    R. Edwards, T. Wirth, J. Label. Compd. Radiopharm. 2015, 58, 183-187. DOI
  180. Synthesis of New Chiral Diaryliodonium Salts
    M. Brown, M. Delorme, F. Malmedy, J. Malmgren, B. Olofsson, T. Wirth, Synlett 2015, 26, 1573-1577. DOI Featured in SYNFORM
  181. Flow Alkylation of Thiols, Phenols, and Amines Using a Heterogenous Base in a Packed-Bed Reactor
    A. Baker, M. Graz, R. Saunders, G. J. S. Evans, I. Pitotti, T. Wirth, J. Flow Chem. 2015, 5, 65-68. DOI
  182. Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement
    J. Tancock, T. Wirth, Molecules 2015, 20, 10866-10872. DOI
  183. Small Organoselenium Compounds: More than just Glutathione Peroxidase Mimics
    T. Wirth, Angew. Chem. 2015, 127, 10212-10214; DOI Angew. Chem. Int. Ed. 2015, 54, 10074-10076. DOI
  184. Solid-Supported Iodonium Salts for Fluorinations
    R. Edwards, W. de Vries, A. D. Westwell, S. Daniels, T. Wirth, Eur. J. Org. Chem. 2015, 6909-6916. DOI
  185. Synthesis by Substitution of Other Halogens F. V. Singh, T. Wirth, Science of Synthesis Vol. 35 (Update 2015/2), 2015, 407-414.
  186. Synthesis by Substitution of Oxygen Functionalities
    F. V. Singh, T. Wirth, Science of Synthesis Vol. 35 (Update 2015/2), 2015, 415-435.
  187. Safe handling of diazo reagents through inline analytics and flow chemistry
    S. T. R. Müller, A. Murat, P. Hellier, T. Wirth, Chem. Today 2015, 33(5), 74-77. Link to Publisher
  188. Hypervalent Iodine Chemistry
    Ed. T. Wirth, Topics in Current Chemistry 2016, 373. Publisher Link
  189. Asymmetric Synthesis with Hypervalent Iodine Reagents
    R. Kumar, T. Wirth, Top. Curr. Chem. 2016, 373, 243-262.
  190. Towards a large scale approach to Milnacipran analogues using diazo compounds in flow chemistry
    S. T. R. Müller, A. Murat, P. Hellier, T. Wirth, Org. Process Res. Dev. 2016, 20, 495-502. DOI
  191. Thioamination of Alkenes with Hypervalent Iodine Reagents
    P. Mizar, R. Niebuhr, M. Hutchings, U. Farooq, T. Wirth, Chem. Eur. J. 2016, 22, 1614-1617. DOI oa
  192. Enantioselective Oxidative Rearrangements with Chiral Hypervalent Iodine Reagents
    M. Brown, R. Kumar, J. Rehbein, T. Wirth, Chem. Eur. J. 2016, 22, 4030-4035. DOI  oa COVER PICTURE
  193. A simple set-up for transfer hydrogenations in flow chemistry
    M. Hutchings, T. Wirth, Synlett 2016, 27, 1832-1835. DOI Highlighted in Synfacts
  194. Safe use of Nitromethane for Aldol Reactions in Flow
    M. Hutchings, T. Wirth, J. Flow Chem. 2016, 6, 202-205. DOI
  195. Ethyl lithiodiazoacetate: Extremely unstable intermediate handled efficiently in flow
    S. T. R. Müller, T. Hokamp, S. Ehrmann, P. Hellier, T. Wirth, Chem. Eur. J. 2016, 22, 11940-11942. DOI
  196. Contrasting Frustrated Lewis Pair Reactivity with Selenium- and Boron-Based Lewis Acids
    L. C. Wilkins, B. A. R. Günther, M. Walther, J. R. Lawson, T. Wirth, R. L. Melen, Angew. Chem. 2016, 128, 11462-11465; DOI Angew. Chem. Int. Ed. 2016, 55, 11292-11295. DOI
  197. Stereoselective Ketone Rearrangements with Hypervalent Iodine Reagents
    F. Malmedy, T. Wirth, Chem. Eur. J. 2016, 22, 16072-16077. DOI
  198. Novel Organic Synthesis through Ultrafast Chemistry
    T. Wirth, Angew. Chem. 2017, 129, 698-700; DOI Angew. Chem. Int. Ed. 2017, 56, 682-684. DOI
  199. Optimising Terpene Synthesis with Flow Biocatalysis
    X. Tang, R. K. Allemann, T. Wirth, Eur. J. Org. Chem. 2017, 414-418. DOI       VIDEO (2:37 min)  Featured on the Organic Chemistry Portal
  200. Cyclization of malonate derivatives with iodine(III) reagents
    F. Malmedy, T. Wirth, Eur. J. Org. Chem. 2017, 786-789. DOI
  201. Facile one-pot synthesis of diaryliodonium salts from arenes and aryl iodides with Oxone
    N. Soldatova, P. Postnikov, O. Kukurina, V. V. Zhdankin, A. Yoshimura, T. Wirth, M. S. Yusubov, ChemistryOpen 2017, 6, 18-20. DOI
  202. Iodoaminations of Alkenes
    P. Mizar, T. Wirth, Synthesis 2017, 49, 981-986. DOI
  203. An efficient chemoenzymatic synthesis of dihydroartemisinic aldehyde
    M. Demiray, X. Tang, T. Wirth, J. A. Faraldos, R. K. Allemann, Angew. Chem. 2017, 129, 4411-4415; DOI Angew. Chem. Int. Ed. 2017, 56, 4347-4350. DOI   oa
  204. Enantioselective Synthesis of trans-2,3-Dihydro-1H-indoles through C–H Insertion of α-Diazocarbonyl Compounds
    M. Santi, S. T. R. Müller, A. A. Folgueiras-Amador, A. Uttry, P. Hellier, T. Wirth, Eur. J. Org. Chem. 2017, 1889-1893. DOI
  205. Silyl Sulfides and Selenides
    A. Baker, T. Wirth, Science of Synthesis Knowledge Updates, 2017, 1, 189-202. DOI
  206. Synthesis of 1-Chloro-n-Heteroatom-Functionalized Alkanes by Addition across C=C Bonds
    F. V. Singh, T. Wirth, Science of Synthesis Knowledge Updates, 2017, 1, 403-442. DOI
  207. Organic synthesis in flow for medicinal chemistry
    T. Wirth, Bioorg. Med. Chem. 2017, 25, 6179. DOI
  208. Electron-deficient Chiral Lactic Acid-based Hypervalent Iodine Reagents
    J. Qurban, M. Elsherbini, T. Wirth, J. Org. Chem. 2017, 82, 11872-11876. DOI
  209. An Easy-to-Machine Electrochemical Flow Microreactor: Efficient Isoindolinone Synthesis and Flow Functionalization
    A. A. Folgueiras-Amador, K. Philipps, S. Guilbaud, J. Poelakker, T. Wirth, Angew. Chem. 2017, 129, 15648-15653; DOI Angew. Chem. Int. Ed. 2017, 56, 15446-15450. DOIoa
  210. Integration of Flow Chemistry in Multistep Syntheses, T. Wirth, Eur. J. Org. Chem. 2017, 6464. DOI
  211. Guest Editor Profile, T. Wirth, Eur. J. Org. Chem. 2017, 6465. DOI
  212. Acid-Catalyzed Tandem Process for the One-Pot Synthesis of Oxazolidines
    A. H. Aldimairi, D. W. Knight, T. Wirth, Synlett 2017, 28, 2976-2978. DOI
  213. Catalytic Oxidations with Hypervalent Iodine
    F. V. Singh, T. Wirth, Science of Synthesis: Catalytic Oxidation in Organic Synthesis, 2017, 1, 29-62. DOI
  214. Perspectives in Flow Electrochemistry
    A. A. Folgueiras-Amador, T. Wirth, J. Flow Chem. 2017, 7, 94-95. DOI oa
  215. Synthesis of Organoselenium Compounds with Potential Biological Activities
    F. V. Singh, T. Wirth, in Organoselenium Compounds in Biology and Medicine: Synthesis, Biological and Therapeutic Treatments, Eds. V. K. Jain, K. I. Priyadarsini, The Royal Society of Chemistry, 2018, 77-121.
  216. Catalyst- and Supporting Electrolyte-Free Electrosynthesis of Benzothiazoles and Thiazolopyridines in Continuous Flow
    A. A. Folgueiras-Amador, X.-Y. Qian, H.-C. Xu, T. Wirth, Chem. Eur. J. 2018, 24, 487-491. DOI Highlighted in Synfacts
  217. Reactions of 1-Arylbenziodoxolones with Azide Anion: Experimental and Computational Study of Substituent Effects
    M. S. Yusubov, N. S. Soldatova, P. S. Postnikov, R. R. Valiev, D. Y. Svitich, R. Y. Yusubova, A. Yoshimura, T. Wirth, V. V. Zhdankin, Eur. J. Org. Chem. 2018, 640-647. DOI
  218. Iodine Monoacetate for Efficient Oxyiodinations of Alkenes and Alkynes
    T. Hokamp, A. T. Storm, M. Yusubov, T. Wirth, Synlett 2018, 29, 415-418. DOI
  219. One-pot synthesis of diaryliodonium salts from arenes and aryl iodides with Oxone–sulfuric acid
    N. Soldatova, P. Postnikov, O. Kukurina, V. V. Zhdankin, A. Yoshimura, T. Wirth, M. S. Yusubov, Beilstein J. Org. Chem. 2018, 14, 849-855. DOI
  220. Concise Synthesis of Artemisinin from a Farnesyl Diphosphate Analogue
    X. Tang, M. Demiray, R. K. Allemann, T. Wirth, Bioorg. Med. Chem. 2018, 26, 1314-1319. DOI
  221. Selective Oxidation of Sulfides in Flow Chemistry
    F. Silva, A. Baker, J. Stansall, W. Michalska, M. S. Yusubov, M. Graz, R. Saunders, G. J. S. Evans, T. Wirth, Eur. J. Org. Chem. 2018, 2134-2137. DOI
  222. Mechanochemical Synthesis of N-tert-Butanesulfinyl Imines Under Metal-Free Conditions
    M. Elsherbini, T. Wirth, Tetrahedron 2018, 74, 3101-3106. DOI
  223. Alternative Strategies with Iodine: Fast Access to Previously Inaccessible Iodine(III) Compounds
    T. Hokamp, L. Mollari, L. C. Wilkins, R. L. Melen, T. Wirth, Angew. Chem. 2018, 130, 8438-8442; DOI Angew. Chem. Int. Ed. 2018, 57, 8306 -8309. DOI
  224. Safe use of Hazardous Chemicals in Flow
    Md T. Rahman, T. Wirth,Top. Heterocycl. Chem. 2018, 56, 343-373.  DOI
  225. Stereoselective reactions
    F. V. Singh, T. Wirth, in Patai’s Chemistry of Functional Groups, The Chemistry of Hypervalent Halogen Compounds , Eds. I. Marek, B. Olofsson, Z. Rappoport, John Wiley & Sons, Ltd: Chichester,  2018. DOI
  226. Preparation and X-ray structure of 2-iodoxybenzenesulfonic acid (IBS) – a powerful hypervalent iodine(V) oxidant
    I. A. Mironova, P. S. Postnikov, R. Y. Yusubova, A. Yoshimura, T. Wirth, V. V. Zhdankin, V. N. Nemykin, M. S. Yusubov, Beilstein J. Org. Chem. 2018, 14, 1854-1858. DOI
  227. Hypervalent Iodine Reagents by Anodic Oxidation: a Powerful Green Synthesis
    M. Elsherbini, T. Wirth, Chem. Eur. J. 2018, 24, 13399-13407. DOI
  228. Short Total Synthesis of Ajoene
    F. Silva, S. S. Khokhar, D. M. Williams, R. Saunders, G. J. S. Evans, M. Graz, T. Wirth, Angew. Chem. 2018, 130, 12470-12473; DOI Angew. Chem. Int. Ed. 2018, 57, 12290-12293. DOIoa
  229. Electrosynthesis in Continuous Flow
    A. A. Folgueiras-Amador, T. Wirth, Science of Synthesis, Flow Chemistry in Organic Synthesis, 2018, 147-189. DOI
  230. Organoselenium Chemistry
    F. V. Singh, T. Wirth, in Encyclopedia of Inorganic and Bioinorganic Chemistry, John Wiley & Sons, Ltd: Chichester, 2018. DOI
  231. Enantioselective Electrochemical Lactonization Using Chiral Iodoarenes as Mediators
    W.-C. Gao, Z.-Y. Xiong, S. Pirhaghani, T. Wirth, Synthesis 2019, 51, 276-284. DOIoa
  232. Selenium and Tellurium Electrophiles in Organic Synthesis
    F. V. Singh, T. Wirth in Selenium and Tellurium Reagents, Eds. R. Laitinen, R. Oilunkaniemi, De Gruyter, 2019, pp. 243-299.
    F. V. Singh, T. Wirth, Phys. Sci. Rev. 2019, 4. DOI
  233. Efficient Electrosynthesis of Thiazolidin-2-imines via Oxysulfurization of Thiourea-Tethered Terminal Alkenes using the Flow Microreactor
    M. Islam, B. M. Kariuki, Z. Shafiq, T. Wirth, N. Ahmed, Eur. J. Org. Chem. 2019, 1371-1376. DOI
  234. Selenium Reagents as Catalysts
    F. V. Singh, T. Wirth, Catal. Sci. Technol. 2019, 9, 1073-1091. DOI
  235. Meet the Board of ChemistryOpen: Thomas Wirth
    T. Wirth, ChemistryOpen 2019, 8, 251. DOI
  236. Flow Synthesis of Iodonium Trifluoroacetates through Direct Oxidation of Iodoarenes by Oxone®
    N. S. Soldatova, P. S. Postnikov, M. S. Yusubov, T. Wirth, Eur. J. Org. Chem. 2019, 2081-2088. DOI
  237. Morpholin-2-one Derivatives via Intramolecular Acid-Catalyzed Hydroamination
    A. H. Aldimairi, D. W. Knight, T. Wirth, Synthesis 2019, 51, 1643-1648. DOI
  238. Metal-Free Tandem Rearrangement/Lactonization: Access to 3,3-Disubstituted Benzofuran-2-(3H)-ones
    M. Santi, D. M. C. Ould, J. Wenz, Y. Soltani, R. L. Melen, T. Wirth, Angew. Chem. 2019, 131, 7943-7947; DOI Angew. Chem. Int. Ed. 2019, 58, 7861-7865. DOI
  239. Efficient Flow Electrochemical Alkoxylation of Pyrrolidine-1-carbaldehyde
    N. Amri, R. A. Skilton, D. Guthrie, T. Wirth, Synlett 2019, 30, 1183-1186. DOI
  240. 2-Iodoxybenzoic acid ditriflate: the most powerful hypervalent iodine(V) oxidant
    M. S. Yusubov, N. S. Soldatova, P. Postnikov, R. R. Valiev, A. Yoshimura, T. Wirth, V. Nemykin, V. V. Zhdankin, Chem. Commun. 2019, 55, 7760-7763.  DOI   Highlighted in Chemistry World  
  241. Continuous Flow Electrochemical Generator of Hypervalent Iodine Reagents: Synthetic Applications
    M. Elsherbini, B. Winterson, H. Alharbi, A. A. Folgueiras-Amador, C. Génot, T. Wirth, Angew. Chem. 2019, 131, 9916-9920; DOI  Angew. Chem. Int. Ed. 2019, 58, 9811-9815. DOI Highlighted in Synfacts
  242. Structurally Defined α-Tetralol-Based Chiral Hypervalent Iodine Reagents
    T. Hokamp, T. Wirth, J. Org. Chem. 2019, 84, 8674-8682. DOI
  243. Synthesis, characterisation, and reactivity of novel pseudocyclic hypervalent iodine reagents with heteroaryl carbonyl substituents
    J. Qurban, M. Elsherbini, H. Alharbi, T. Wirth, Chem. Commun. 2019, 55, 7998-8000. DOI
  244. Reactions of hydrazones and hydrazides with Lewis acidic boranes
    T. A. Gazis, A. Dasgupta, M. S. Hill, J. M. Rawson, T. Wirth, R. L. Melen, Dalton Trans. 2019, 48, 12391-12395. DOI
  245. ‘Dark’ Singlet Oxygen Made Easy
    M. Elsherbini, R. K. Allemann, T. Wirth, Chem. Eur. J. 2019, 25, 12486-12490. DOI Highlighted in OPRD
  246. Electrochemistry under Flow Conditions
    A. A. Folgueiras-Amador, T. Wirth in Flow Chemistry: Integrated Approaches for Practical Applications, Eds: S. V. Luis, E. Garcia-Verdugo, RSC Publishing, 2019, pp. 153-198. DOI
  247. Manganese-Catalyzed Electrochemical Deconstructive Chlorination of Cycloalkanols via Alkoxy Radicals
    B. D. W. Allen, M. D. Hareram, A. C. Seastram, T. McBride, T. Wirth, D. L. Browne, L. C. Morrill, Org. Lett. 2019, 21, 9241-9246. DOI
  248. Electroorganic Synthesis under Flow Conditions
    M. Elsherbini, T. Wirth, Acc. Chem. Res. 2019, 52, 3287-3296. DOI
  249. Memory of Chirality in Flow Electrochemistry: Fast Optimisation with DoE and Online 2D-HPLC
    M. Santi, J. Seitz, R. Cicala, T. Hardwick, N. Ahmed, T. Wirth, Chem. Eur. J. 2019, 25, 16230-16235. DOI
  250. 1,3-Carboboration of Iodonium Ylides
    T. A. Gazis, B. A. Mohajeri, D. Willcox, D. M. C. Ould, J. Wenz, J. M. Rawson, M. S. Hill, T. Wirth, R. L. Melen, Chem. Commun. 2020, 56, 3345-3348. DOI
  251. Immobilised Enzymes for Sesquiterpene Synthesis in Batch and Flow Systems
    D. Valikhani, P. L. Srivastava, R. K. Allemann, T. Wirth, ChemCatChem 2020, 12, 2194-2197. DOI
  252. Automated Electrochemical Selenenylations
    N. Amri, T. Wirth, Synthesis 2020, 52, 1751-1761. DOI
  253. 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
    M. Yamamoto Raynbird, F. Silva, H. Smallman, S. S. Khokhar, D. Neef, G. J. S. Evans, T. Wirth, Chem. Eur. J. 2020, 26, 8363-8367. DOI
  254. Hypervalent Iodine(III)-Catalysed Enantioselective α-Acetoxylation of Ketones
    T. Hokamp, T. Wirth, Chem. Eur. J. 2020, 26, 10417-10421. DOI
  255. Selective hydroboration – oxidation of terminal alkenes under flow conditions
    M. Elsherbini, F. Huynh, A. Dunbabin, R. K. Allemann, T. Wirth, Chem. Eur. J. 2020, 26, 11423-11425. DOI Highlighted in Synfacts
  256. Accelerating biphasic biocatalysis through new process windows
    F. Huynh, M. Tailby, A. Finniear, K. Stephens, R. K Allemann, T. Wirth, Angew. Chem. 2020, 132, 16632-16637; DOI  Angew. Chem. Int. Ed. 2020, 59, 16490-16495. DOI
  257. Memory of chirality in a room temperature flow electrochemical reactor
    T. Hardwick, R. Cicala, T. Wirth, N. Ahmed, Sci. Rep. 2020, 10, 16627. DOI
  258. Accelerating Electrochemical Synthesis through Automated Flow: Efficient Synthesis of Chalcogenophosphites
    N. Amri, T. Wirth, Synlett 2020, 31, 1894-1898. DOI
  259. Synthesis of Ajoene Analogues by Novel Synthetic Strategies
    M. Yamamoto Raynbird, S. S. Khokhar, D. Neef, G. J. S. Evans, T. Wirth, Chem. Eur. J. 2021, 27, 3008–3012. DOI
  260. C–N Axial Chiral Hypervalent Iodine Reagents: Catalytic Stereoselective α-Oxytosylation of Ketones
    H. Alharbi, M. Elsherbini, J. Qurban, T. Wirth, Chem. Eur. J. 2021, 27, 4317–4321. DOI
  261. Chiral Triptycenes: Concepts, Progress and Prospects
    N. Khan, T. Wirth, Chem. Eur. J. 2021, 27, 7059–7068. DOI
  262. Iodine(III) Mediators in Electrochemical Batch and Flow Reactions
    T. Wirth, Curr. Opin. Electrochem. 2021, 28, 100701. DOI
  263. Recent Advances in Asymmetric Functionalization of Olefins Induced by Chiral Hypervalent Iodine Reagents
    H. Zhang, T. Wirth, Chin. J. Org. Chem. 2021, 41, 56–79. DOI
  264. Recent Advances in the Electrochemical Synthesis of Organosulfur Compounds
    N. Amri, T. Wirth, Chem. Rec. 2021, 21, 2526–2537. DOI
  265. Electrochemistry in Flow for Drug Discovery
    B. Winterson, T. Wirth, Top. Med. Chem. 2021, 121–172. DOI
  266. Reactions Promoted by Hypervalent Iodine Reagents and Boron Lewis Acids
    A. Dasgupta, C. Thiehoff, P. D. Newman, T. Wirth, R. L. Melen, Org. Biomol. Chem. 2021, 19, 4852–4865. DOI
  267. Hypervalent iodine chemistry and light: photochemical reactions involving hypervalent iodine chemistry
    F. V. Singh, T. Wirth, ARKIVOC 2021, vii, 12–47. DOI
  268. Flow Electrochemistry: A Safe Tool for Fluorine Chemistry
    B. Winterson, T. Renningholtz, T. Wirth, Chem. Sci. 2021, 12, 9053–9059. DOI
  269. Flow Electrosynthesis of Sulfoxides, Sulfones and Sulfoximines without Supporting Electrolytes
    N. Amri, T. Wirth, J. Org. Chem. 2021, 86, 15961–15972. DOI
  270. Electrochemical Bromofunctionalization of Alkenes in a Flow Reactor
    J. Seitz, T. Wirth, Org. Biomol. Chem. 2021, 19, 6892–6896. DOI
  271. Hypervalent Bromine(III) Compounds: Synthesis, Applications, Prospects
    B. Winterson, T. Patra, T. Wirth, Synthesis 2022, 54, 1261–1271. DOI
  272. Chiral Ligands in Hypervalent Iodine Compounds: Synthesis and Structures of Binaphthyl-based λ3-Iodanes
    H. Zhang, R. A. Cormanich, T. Wirth, Chem. Eur. J. 2022, 28, e202103623. DOI
  273. Oxidation of BINOLs by Hypervalent Iodine Reagents: Facile Synthesis of Xanthenes and Lactones
    H. Zhang, T. Wirth, Chem. Eur. J. 2022, 28, e202200181. DOI
  274. Zwitterionic Iodonium Species Afford Halogen Bond-Based Porous Organic Frameworks
    N. 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. 2022, 13, 5650–5658. DOI
  275. Biomimetic Total Synthesis of (–)-Galanthamine via Intramolecular Anodic Aryl-Phenol Coupling
    Z. Xiong, F. Weidlich, C. Sanchez, T. Wirth, Org. Biomol. Chem. 2022, 20, 4123–4127. DOI
  276. Borane promoted aryl transfer reaction for the synthesis of α-aryl functionalised β-hydroxy and β-keto esters
    T. Kaehler, J. Lorenz, D. M. C. Ould, D. Engl, M. Santi, L. Gierlichs, T. Wirth, R. L. Melen, Org. Biomol. Chem. 2022, 20, 4298–4302. DOI
  277. Electrochemical Deconstructive Functionalization of Cycloalkanols via Alkoxy Radicals Enabled by Proton-Coupled Electron Transfer
    M. 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, Org. Lett. 2022, 24, 3890–3895. DOI
  278. Chiral Iodotriptycenes: Synthesis and Catalytic Applications
    N. Khan, T. Wirth, ChemistryOpen 2022, 11, e202200145. DOI
  279. Progress in organocatalysis with hypervalent iodine catalysts
    F. V. Singh, S. E. Shetgaonkar, M. Krishnan, T. Wirth, Chem. Soc. Rev. 2022, 51, 8102–8139. DOI
  280. Oxidative Cleavage of Alkenes by Photosensitized Nitroarenes
    T. Patra, T. Wirth, Angew. Chem. 2022, 134, e202213772. DOI;  Angew. Chem. Int. Ed. 2022, 61, e202213772. DOI
  281. Two-step continuous-flow synthesis of 6-membered cyclic iodonium salts via anodic oxidation
    J. Spils, T. Wirth, B. Nachtsheim, Beilstein J. Org. Chem. 2023, 19, 27–32. DOI
  282. Sulfur-based chiral iodoarenes: An underexplored class of chiral hypervalent iodine reagents
    M. Elsherbini, A. Osi, H. Alharbi, F. Karam, T. Wirth, Synthesis 2023, 55, 307–314. DOI
  283. Alkene reactions with superoxide radical anions in flow electrochemistry
    R. Ali, T. Patra, T. Wirth, Faraday Discussions 2023, DOI
  284. Flow Electrochemistry for the N-Nitrosation of Secondary Amines
    R. Ali, R. Babaahmadi, M. Didsbury, R. Stephens, R. L. Melen, T. Wirth, Chem. Eur. J. 2023, 29, e202300957. DOI
  285. B(3,4,5-F3H2C6)3 Lewis acid-catalysed C3-allylation of indoles
    N. Alotaibi, R. Babaahmadi, M. Pramanik, T. Kaehler, A. Dasgupta, E. Richards, A. Ariafard, T. Wirth, R. L. Melen, Dalton Trans. 2023, 52, 5039–5043. DOI
  286. Hypervalent Iodine in Electrochemical Reactions: Advantages and Prospects
    T. Wirth, SIS Lett. 2023, No. 24, 2–6.
  287. Synthesis of Chiral Iodoaniline-Lactate Based Catalysts for the α-Functionalization of Ketones
    R. Alkahtani, T. Wirth, ACS Org. Inorg. Au 2023, 3, 209–216. DOI
  288. Hypervalent Halogen Compounds in Electrochemical Reactions: Advantages and Prospects
    B. Winterson, D. Bhattacherjee, T. Wirth, Adv. Synth. Catal. 2023, 365, 2676–2689. DOI
  289. Selected Diastereoselective Reactions: Hypervalent iodine chemistry
    F. V. Singh, T. Wirth in Comprehensive Chirality: Chiral Pool and Diastereoselective Synthesis, Ed. J. Cossy, Elsevier, in press. DOI
  290. Isodesmic metathesis chemistry: A novel way to recycle P(V)
    T. Boruah, R. L. Melen, T. Wirth, Chem Catal. 2023, 3, 100731. DOI