Publications 2016–2017


206. Concise Synthesis of Artemisinin from a Farnesyl Diphosphate Analogue
X. Tang, M. Demiray, R. K. Allemann, T. Wirth, Bioorg. Med. Chem. 2017, in press. DOI

205. 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

204. An efficient chemoenzymatic synthesis of dihydroartemisinic aldehyde
M. Demiray, X. Tang, T. Wirth, J. A. Faraldos, R. K. Allemann, Angew. Chem. 2017129, 4411-4415; DOI Angew. Chem. Int. Ed. 2017, 56, 4347-4350. DOI

203. Catalytic Oxidations with Hypervalent Iodine
F. V. Singh, T. Wirth, Science of Synthesis2017, in press.

202. Iodoaminations of Alkenes
P. Mizar, T. Wirth, Synthesis 201749, 981-986. 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

200. Cyclization of malonate derivatives with iodine(III) reagents
F. Malmedy, T. Wirth, Eur. J. Org. Chem. 2017, 786-789. 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)

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


197. Stereoselective Ketone Rearrangements with Hypervalent Iodine Reagents
F. Malmedy, T. Wirth, Chem. Eur. J. 201622, 16072-16077. 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

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. 201622, 11940-11942. DOI

194. Safe use of Nitromethane for Aldol Reactions in Flow
M. Hutchings, T. Wirth, J. Flow Chem. 2016, 6, 202-205. DOI

193. A simple set-up for transfer hydrogenations in flow chemistry
M. Hutchings, T. Wirth, Synlett 2016, 27, 1832-1835. DOI Highlighted in Synfacts

192. Enantioselective Oxidative Rearrangements with Chiral Hypervalent Iodine Reagents
M. Brown, R. Kumar, J. Rehbein, T. Wirth, Chem. Eur. J. 201622, 4030-4035. DOI  oa COVER PICTURE

191. Thioamination of Alkenes with Hypervalent Iodine Reagents
P. Mizar, R. Niebuhr, M. Hutchings, U. Farooq, T. Wirth, Chem. Eur. J. 201622, 1614-1617. DOI   

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

189. Asymmetric Synthesis with Hypervalent Iodine Reagents
R. Kumar, T. Wirth, Top. Curr. Chem. 2016, 373, 243-262. DOI

188. Hypervalent Iodine Chemistry
Ed. T. Wirth, Topics in Current Chemistry 2016, 373Publisher Link