Vyhledat publikace
Kováč, O.; Zálešák, F.; Bon, D.J.-Y.D; Roiser, L.; Baar, L.V.; Waser, M.; Pospíšil, J.
risubstituted highly activated benzo[d]thiazol-2-yl-sulfone-containing olefins as building blocks in organic synthesis
J. Org. Chem. 2020, 85 (n/a), 7192-7206. DOI: 10.1021/acs.joc.0c00571
Mathieu, A.S.; Dobrev, P.I.; Tarkowská, D.; Pospíšil, J.; Motyka, V.; Jacquemin, G.; Quinet, M.; Lutts, S.
Phytohormone profile and CiFL1 expression in young seedlings of Cichorium intybus L. var sativum exposed to high temperature in relation to vernalization and de-vernalization processes
Environ. Exp. Bot. 2020, 178 (n/a), 104127 (1-13). DOI: 10.1016/j.envexpbot.2020.104127
Zielke, K.; Kováč, O.; Winter, M.; Pospíšil, J.; Waser, M.
Enantioselective Catalytic [4+1]‐Cyclization of ortho‐Hydroxy‐para‐Quinone Methides with Allenoates
Chem. Eur. J. 2019, 25 (34), 8163-8168. DOI: 10.1002/chem.201901784
Zálešák, F.; Bon, D. J.-Y. D.; Pospíšil, J.
Lignans and Neolignans: plant secondary metabolites as a reservoir of biologically active substances
Pharmacol. Res. 2019, 146 (n/a), 104284(1-27). DOI: 10.1016/j.phrs.2019.104284
Zhu, Q.; Gallemí, M.; Pospíšil, J.; Žádníková, P.; Strnad, M.; Benková, E.
Root gravity response module guides differential growth determining both root bending and apical hook formation
Development 2019, 146 (17), dev175919. DOI: 10.1242/dev.175919
Béres, T.; Dragull, K.; Pospíšil, J.; Tarkowská, D.; Dančák, M.; Bíba, O.; Tarkowski, P.; Doležal, K.; Strnad, M.
Quantitative Analysis of Ingenol in Euphorbia species via Validated Isotope Dilution Ultra-high Performance Liquid Chromatography Tandem Mass Spectrometry
Phytochem. Anal. 2018, 29 (1), 23-29. DOI: 10.1002/pca.2711
Barbuščáková, Z.; Kozubíková, H.; Zálešák, F.; Doležal, K.; Pospíšil, J.
General approach to neoliganane-core of the boehmenan natural product family
Monatsh. Chem. 2018, 149 (4), 737-748. DOI: 10.1007/s00706-017-2132-4
Bon, D. J.-Y. D; Kováč, O.; Ferugová, V.; Zálešák, F.; Pospíšil, J.
One and two-carbon homologation of primary and secondary alcohols to corresponding carboxylic esters using β-carbonyl BT sulfones as a common intermediate
J. Org. Chem. 2018, 83 (9), 4990-5001. DOI: 10.1021/acs.joc.8b00112
Konrádová, D.; Bon, D. J.-Y. D.; Pospíšil, J.
1-(Phenylsulfonyl)-3-oxabicyclo[3.1.0]hexan-2-one as a building block in organic synthesis
J. Org. Chem. 2018, 83 (12229), 12229-12238. DOI: 10.1021/acs.joc.8b01625
Konrádová, D.; Kozubíková, H.; Doležal, K.; Pospíšil, J.
Microwave-Assisted Synthesis of Phenylpropanoids and Coumarins: Total Synthesis of Osthol
Eur. J. Org. Chem. 2017, 2017 (35), 5204–5213. DOI: 10.1002/ejoc.201701021