Post-doctoral Studies:
(9) Enantioselective Synthesis of the Unsaturated Fragment of Callyspongiolide.
Matoušová, E.; Koukal, P.; Formánek, B.; Kotora, M. Org. Lett. 2016, 18 (21), 5656–5659.
(8) [2+2+2]-Cyclotrimerization of 1-Cyclopropyl-1,6-diynes with Alkynes: Formation of Cyclopropylarenes.
Matoušová, E.; Gyepes, R.; Císařová, I.; Kotora, M. Adv. Synth. Catal. 2016, 358 (2), 254–267.
(7) A Total Synthesis of Galanthamine Involving De Novo Construction of the Aromatic C-Ring.
Nugent, J.; Matoušová, E.; Banwell, M. G. Eur. J. Org. Chem. 2015, 2015 (17), 3771–3778.
(6) The Palladium-Catalysed Intramolecular Alder-ene (IMAE) Reactions of Certain Heteroatom-Linked 1,6-Enynes: The Formation of Hexahydro-Indoles and -Benzofurans.
Crisp, A. L.; Li, J.; Lan, P.; Nugent, J.; Matoušová, E.; Banwell, M. G. Aust. J. Chem. 2015, 68 (8), 1183–1189.
DOI: 10.1071/CH15340
(5) Devising New Syntheses of the Alkaloid Galanthamine, a Potent and Clinically Deployed Inhibitor of Acetylcholine Esterase.
Banwell, M. G.; Buckler, J.; Jackson, C. J.; Lan, P.; Ma, X.; Matoušová, E.; Nugent, J. In Strategies and Tactics in Organic Synthesis; Academic Press: Oxford, 2015; Vol. 11, pp 29–50.
ISBN: 978-0-08-100023-6
(4) A Chemoenzymatic Total Synthesis of the Protoilludane Aryl Ester (+)-Armillarivin.
Schwartz, B. D.; Matoušová, E.; White, R.; Banwell, M. G.; Willis, A. C. Org. Lett. 2013, 15 (8), 1934–1937.
PhD Studies:
(3) Substrate Control in the Gold(I)-Catalyzed Cyclization of β-Propargylamino Acrylic Esters and Further Transformations of the Resultant Dihydropyridines.
Mikušek, J.; Matouš, P.; Matoušová, E.; Janoušek, M.; Kuneš, J.; Pour, M. Adv. Synth. Catal. 2016, 358 (18), 2912–2922.
(2) TFP as a ligand in Au(I)-catalyzed dihydropyran synthesis. Unprecedented rearrangement of dihydropyrans into cyclopentenones.
Matoušová, E.; Růžička, A.; Kuneš, J.; Králová, J.; Pour, M. Chem. Commun. 2011, 47 (33), 9390–9392.
(1) Synthesis and biological activity of desmethoxy analogues of coruscanone A.
Tichotová, L.; Matoušová, E.; Špulák, M.; Kuneš, J.; Votruba, I.; Buchta, V.; Pour, M. Bioorg. Med. Chem. Lett. 2011, 21 (20), 6062–6066.