Publications 2023–2024


301. Deville Rebooted – Practical N2O5 Synthesis
L. E. Edwards, B. M. Kariuki, M. Didsbury, C. D. Jones, T. Wirth, Chem. Commun. 2024, in press. DOI

300. Diverse Reactivity of Amidinate-Supported Boron Centers with the Hypersilyl Anion and Access to a Monomeric Secondary Boron Hydride
S. Pahar, Y. van Ingen, R. Babaahmadi, B. M. Kariuki, T. Wirth, E. Richards, R. L. Melen, Inorg. Chem. 202463, 8302–8311. DOI

299. Continuous Flow Electroselenocyclization of Allylamides and Unsaturated Oximes to Selenofunctionalized Oxazolines and Isoxazolines
O. Alzaidi, T. Wirth, ACS Org. Inorg. Au 20244, in pressDOI

298. Non-Conventional Methodologies for the Synthesis of N-Nitrosamines
R. Ali, C. Wolfe, T. Wirth, Chem. Meth. 2024, 4, e202300053. DOI

297. Biphasic Organic Synthesis with Continuous Electro-Flow
P. Mizar, S. Arepally, T. Wirth, Curr. Opin. Green Sust. Chem. 2024, 46, 100896. DOI

296. B(C6F5)3-Catalysed Alkylation of Imidazo[1,2-a]pyridines Using α,β-Unsaturated Ketones
N. Alotaibi, R. Babaahmadi, M. Pramanik, S. Das, B. M. Kariuki, E. Richards, T. Wirth, R. L. Melen, Eur. J. Org. Chem. 2024, 27, e202400022. DOI

295. An un-forgotten classic: the nitro-Mannich reaction between nitrones and silyl nitronates catalysed by B(C6F5)3
M. Guerzoni, Y. van Ingen, R. Babaahmadi, T. Wirth, E. Richards and R. L. Melen, Chem. Sci. 2024, 15, 2648–2654. DOI


294. Advances in CO2 activation by frustrated Lewis pairs: from stoichiometric to catalytic reactions
N. Khan, Y. van Ingen, T. Boruah, A. McLauchlan, T. Wirth, R. L. Melen, Chem. Sci. 202314, 13661–13695. DOI

293. Electric-field-assisted anion-π catalysis on carbon nanotubes in electrochemical microfluidic devices
 M. Á. Gutiérrez López, R. Ali, M.-L. Tan, N. Sakai, T. Wirth, S. Matile, Sci. Adv. 2023, 9, eadj5502. DOI

292. Isodesmic metathesis chemistry: A novel way to recycle P(V)
T. Boruah, R. L. Melen, T. Wirth, Chem Catal. 20233, 100731. DOI

291. 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. Hypervalent Halogen Compounds in Electrochemical Reactions: Advantages and Prospects
B. Winterson, D. Bhattacherjee, T. Wirth, Adv. Synth. Catal. 2023365, 2676–2689. DOI

289. Synthesis of Chiral Iodoaniline-Lactate Based Catalysts for the α-Functionalization of Ketones
R. Alkahtani, T. Wirth, ACS Org. Inorg. Au 20233, 209–216DOI

288. Hypervalent Iodine in Electrochemical Reactions: Advantages and Prospects
T. Wirth, SIS Lett. 2023No. 24, 2–6.

287. 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. 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. Flow cells and reactor design: general discussion
A. Alkayal, M. Avanthay, B. Batanero, P. Broersen, R. C. D. Brown, L. Chen, P.-C. Chuang, T. Fuchigami, S. Inagi, D. Kalyani, K. Lam, M. Landis, T. L. Liu, M. J. Milner, R. Price, N. Shida, T. Wirth, Faraday Discuss. 2023, 247, 333–341. DOI

284. Alkene reactions with superoxide radical anions in flow electrochemistry
R. Ali, T. Patra, T. Wirth, Faraday Discuss. 2023, 247, 297–301. DOI

283. New strategies in organic electrosynthesis: general discussion
M. Avanthay, J. A. Beeler, B. Batanero, D. 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-Villaseñor, T. Wirth, Faraday Discuss. 2023, 247, 125–131. 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

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