Publications

Publications

For my post-doctoral, PhD or master publications, scroll down.

Books and chapters are located at the end. 

2024
  1. „Julia-Kocienski-like connective C-C and C=C bond-forming reaction„
    Bon, D.J.-Y.D.; Chrenko, D.; Kováč, O.; Ferugová, V.; Lasák, P.; Fuksová, M.; Zálešák, F.; Pospíšil, J. Adv. Synth. Catal. 2024, 366, 480-487.
    DOI: 10.1002/adsc.202301054
2023
  1. „Responses to abiotic and biotic stresses – from the cellular level to fruit development – contributions of the Czech Centre for Experimental Plant Biology„
    Vaňková, R., Burketová, L., Brzobohatý, B., Černý, M., Hafidh, S., Hejátko, J., Honys, D., Hoyerová, K., Juříček, M., Martinec, J., Moravec, T., Pečenková, T., Petrášek, J., Pospíšil, J., Retzer, K., Robert, H. S., Štorchová, H., Vaněk, T., Žárský, V. Biologia Plantarum 2023, 67, 166–174.
    DOI: 10.32615/bp.2023.028
  1. „Enantioselective beta-selective addition of isoxazolidin-5-ones to allenoates
    catalyzed by quaternary ammonium salts    „
    Zebrowski, P.; Rösel, K.; Chrenko, D.; Pospíšil, J.; Waser, M. Synthesis 2023, 55(11), 1706-1713; DOI: 10.1055/a-1948-5493

    Included in Special Issue dedicated to Prof. Cristina Nevado, Recipient of the 2021 Dr. Margaret Faul Women in Chemistry Award

2022
  1. „Sulfated Phenolic Acids in Plants„
    Supikova, K.; Kosinova, A.; Vavrusa, M.; Koplikova, L.; François, A.; Pospisil, J.; Zatloukal, M.; Wever, R.; Hartog, A.; Gruz, J. Planta 2022, 255(6), 124; DOI: 10.1007/s00425-022-03902-6
  1. „Heteroaryl sulfonamide synthesis: scope andlimitations„
    Iakovenko, R. O.; Chrenko, D.; Kristek, J.; Desmedt, E.; Zálešák, F.; De Vleeschouwer, F.; Pospíšil, J. Org. Biomol. Chem. 2022, 20, 3154-3159; DOI: 10.1039/D2OB00345G
2021
  1. „Unified Approach to Benzo[d]thiazol-2-yl-Sulfonamides„
    Zálešák, F.; Kováč, O.; Lachetová, E.; Šťastná, N.; Pospíšil, J. J. Org. Chem. 2021, 86, 11291-11309; DOI: 10.1021/acs.joc.1c00317
2020
  1. „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„
    Mathieu, A.S.; Dobrev, P.I.; Tarkowská, D.; Pospíšil, J.; Motyka, V.; Jacquemin, G.; Quinet, M.; Lutts, S. Environ. Exp. Bot. 2020, 178, 104127; DOI: 10.1016/j.envexpbot.2020.104127
  1. „Trisubstituted highly activated benzo[d]thiazol-2-yl-sulfone-containing olefins as building blocks in organic synthesis„
    Kováč, O.; Zálešák, F.; Bon, D.J.-Y.D; Roiser, L.; Baar, L.V.; Waser, M.; Pospíšil*, J. J. Org. Chem. 2020, 85, 7192-7206; DOI: 10.1021/acs.joc.0c00571.
abstract of the paper
  1. „Diferulate: A Highly Effective Electron Donor„
    Vacek*, J.; Zatloukalová, M.; Vrba, J.; De Vleeschouwer, F.; De Proft, F.; Obluková, M.; Sokolová, R.; Pospíšil*, J. J. Electroanal. Chem. 2020, 869, 113950;
    DOI: 10.1016/j.jelechem.2020.1139501.
  1. „Salicylic Acid Targets Protein Phosphatase 2A to Attenuate Growth in Plants„
    Tan, S.; Abas, M.; Verstraeten, M.; Glanc, M.; Molnár, G.; Hajný, J.; Lasák, P.; Petřík, I.; Russinova, E.; Petrášek, J.; Novák, O.; Pospíšil, J.; Friml*, J. Curr. Biol. 2020, 30, 381-395;
    DOI: 10.1016/j.cub.2019.11.058.
  1. „Rearrangement of Threonine and Serine-Based N-(3-Phenylprop-2-yn-1-yl) Sulfonamides Yields Chiral Pyrrolidin-3-ones“
    Králová, P.; Maloň, M.; Pospíšil, J.; Soural*, M. J. Org. Chem. 2020, 85, 985-993; DOI: 10.1021/acs.joc.9b02932.

2019
  1. „Root gravity response module guides differential growth determining both root bending and apical hook formation“ Zhu, Q.; Gallemí, M.; Pospíšil, J.; Žádníková, P.; Strnad, M.; Benková*, E. J. Development 2019, 146, dev175919; DOI: 10.1242/dev.175919.
  1. „Lignans and Neolignans: Plant secondary metabolites as a reservoir of biologically active substances
    Zálešák, F.; Bon, D. J.-Y. D.; Pospíšil*, J. Pharmacolog. Res. 2019, 146, 104284; DOI: 10.1016/j.phrs.2019.104284.

    Review
  1. „Enantioselective Catalytic [4+1]‐Cyclization of ortho‐Hydroxy‐para‐Quinone Methides with Allenoates“
    Zielke, K.; Kováč, O.; Winter, M.; Pospíšil, J.; Waser*, M. Chem. Eur. J. 2019, 25, 8163-8168; DOI: 10.1002/chem.201901784.

    HOT PAPER

    Included in SYNFACTS 2019, 15(8), 865.

    TOP DOWNLOADED PAPER 2018-2019 in Chemistry – A European Journal

2018
  1. „1-(Phenylsulfonyl)-3-oxabicyclo[3.1.0]hexan-2-one as a Building Block in Organic Synthesis„
    Konrádová, D.; Bon, D.J.-Y.D.; Pospíšil*, J. J. Org. Chem. 2018, 83, 12229-12238; DOI: 10.1021/acs.joc.8b01625.
    Included in SYNFACTS 2018, 14(12), 1233.
  1. „One and Two-Carbon Homologation of Primary and Secondary Alcohols to Corresponding Carboxylic Esters Using β-Carbonyl BT Sulfones as a Common Intermediate„
    Bon, D. J. Y. D.; Kováč, O.; Ferugová, V.; Zálešák, F.; Pospíšil*, J. J. Org. Chem. 2018,83, 4990-5001.
  1. „General approach to neolignan-core of the boehmenan natural product family„
    Barbuščáková, Z.; Kozubíková, H.; Zálešák, F.; Doležal, K.; Pospíšil*, J. Monatsh. Chem.2018, 149, 737-748.
  1. „Quantitative Analysis of Ingenol in Euphorbia species via Validated Isotope Dilution Ultra-high Performance Liquid Chromatography Tandem Mass Spectrometry„
    Béres*, T.; Dragull, K.; Pospíšil, J.; Tarkowská, D.; Dančák, M.; Bíba, O.; Tarkowski, P.; Doležal, K.; Strnad, M. Phytochem. Anal. 2018,29, 23–29.
2017
  1. „Microwave-assisted synthesis of phenylpropanoids and coumarins: total synthesis of Osthol„
    Konrádová, D.; Kozubíková, H.; Doležal, K.; Pospíšil*, J. Eur. J. Org. Chem. 2017, 2017, 5204-5213.
  1. “A convenient method for the preparation of 20-[18O]-labeled ingenol“
    Pospíšil*, J.; Béres, T.; Strnad, M. Tetrahedron Lett. 2017, 58, 1421-1424.
Till 2015
  1. “Determination of free diferulic, disinapic and dicoumaric acids in plants and foods“
    Grúz*, J.; Pospíšil, J.; Kozubíková, H.; Pospíšil, T.; Doležal, K.; Bunzel, M.; Strnad, M. Food Chem. 2015, 171, 280-286.
  1. “On the Origin of E/Z Selectivity in the Modified Julia Olefination: Importance of the Elimination Step“
    Robiette*, R.; Pospíšil*, J. Eur. J. Org. Chem. 2013, 2013, 836-840.
  1. “Julia-Kocienski Reaction-Based 1,3-Diene Synthesis: Aldehyde-Dependent (E,E/E,Z)-Selectivity“
    Billard, F.; Robiette, R.; Pospíšil*, J. J. Org. Chem. 2012,77, 6358-6364.
  1. “Practical Synthesis of b-oxobenzo[d]thiazol sulfones: Scope and Limitations“
    Pospíšil*, J.; Robiette, R.; Sato, H.; Debrus, K. Org. Biomol. Chem. 2012, 10, 1225-1234.
  1. “Planar Chirality of Imidazole-Containing Macrocycles – Understanding and Tuning Atropisomerism”
    Van Den Berge, E.; Pospíšil, J.; Trieu-Van, T.; Collard, L.; Robiette*, R. Eur. J. Org. Chem. 2011, 2011,6649-6655.
  1. “Simple protocol for enhanced (E)-selectivity in Julia-Kocienski reaction“
    Pospíšil*, J. Tetrahedron Lett. 2011, 52, 2348-2352.
  1. “Practical synthesis of β-acyl and β-alkoxycarbonyl heterocyclic sulfones”
    Pospíšil*, J.; Sato, H. J. Org. Chem. 2011,76, 2269-2272.

As Post-doctoral associate

  1. “Total Synthesis and Biological Evaluation of the Cytotoxic Resin Glycosides Ipomoeassin A-F and Analogues”
    Nagano, T.; Pospíšil, J.; Chollet, G.; Schulthoff, S.; Hickmann, V.; Moulin, E.; Herrmann, J.; Müller, R.; Fürstner*, A. Chem. Eur. J. 2009, 15, 9697-9706.
  1. “Total Synthesis of the Aspercyclides“
    Pospíšil, J.; Müller, C.; Fürstner*, A. Chem. Eur. J. 2009, 15, 5956-5968.

As PhD student

  1. “Unexpected nucleophilic behaviour of free-radicals generated from a-iodoketones“
    De Dobbeleer, C.; Pospíšil, J.; De Vleeschouwer, F.; De Proft, F.; Markó*, I. E. Chem. Commun. 2009, 2142-2144.
  1. “Metathesis-based synthesis of 3-methoxy a,b-unsaturated lactones: total synthesis of (R)-kavain and of the C1–C6 fragment of jerangolid D“
    Pospíšil, J.; Markó*. I. E. Tetrahedron Lett. 2008, 49, 1523-1526.
  1. “Total synthesis of Jerangolid D”
    Pospíšil, J.; Markó*, I. E. J. Am. Chem. Soc. 2007, 129, 3516-3517.
    JACS’s 20th most accessed article in 2007, included in 1st issue of JACSβ
  1. “Efficient and stereoselective synthesis of allylic ethers and alcohols”
    Pospíšil, J.; Markó*, I. E. Org. Lett. 2006, 8, 5983-5986.
  1. “Total synthesis of (R)-(+)-goniothalamin and (R)-(+)-goniothalamin oxide: first application of the sulfoxide-modified Julia olefination in total synthesis”
    Pospíšil, J.; Markó*, I. E. Tetrahedron Lett. 2006, 47, 5933-5937.
    Tetrahedron Letters’ 24th hottest article in 2006
  1. “Highly DiastereoselectiveSilyl-Modified Sakurai Multicomponent Reaction”
    Pospíšil, J.; Kumamoto, T.; Markó*, I. E. Angew. Chem. Int. Ed. 2006, 45, 3357 –3360.
  1. “Sulfoxide-modified Julia-Lythgoe olefination: Highly stereoselective di-, tri-, and tetra-substituted double bond formation”
    Pospíšil, J.; Pospíšil, T.; Markó*, I. E. Collect. Czech. Chem. Commun. 2005, 70, 1953-1969.
  1. “Tetracarbonylhydridoferrate Salts: NaHFe(CO)4and KHFe(CO)4”
    Pospíšil*, J. Synlett 2005, 2543-2544.
  1. “Sulfoxides in Julia-Lythgoe Olefination: Efficient and Stereoselective Preparation of Di-, Tri-, and Tetrasubstituted Olefins”
    Pospíšil, J.; Pospíšil, T.; Markó*, I. E. Org. Lett. 2005, 7, 2373-2376.

As master student

  1. “Microwave-assisted Solvent-free Intramolecular 1,3-Dipolar Cycloaddition Reactions Leading to Hexahydrochromeno[4,3-b] pyrroles: Scope and Limitations”
    Pospíšil, J.; Potáček*, M. Tetrahedron 2007, 63, 337-346.
  1. “Amplodine Benzenesulfonate: A Mechanistic Investigation of Its Industrial Preparation via Detritylation of N-tritylamlodipine and Related NMR Studies“
    Furlan, B.; Grdadolnik, S. G.; Hočevar, S.; Kocjan, D.; Levec, J.; Maskill, H.; Navrátilová, H.; Pospíšil, J.; Potáček, M.; Urleb*, U.; Žmitek*, J. Croat. Chem. Acta 2009, 82, 299-309.
  1. “A solvent-free method for substituted imidazolidin- 4-ones synthesis”
    Pospíšil, J.; Potáček*, M. Heterocycles 2004, 63, 1165-1173.
  1. “Microwave-assisted solvent-free synthesis of hexahydrochromeno-[4,3-b] pyrroles”
    Pospíšil, J.; Potáček*, M. Eur. J. Org. Chem. 2004, 2004, 710-716.
  1. “Studies on the DNA-damaging properties of the endogenous mutagen fecapentaene-12”
    Szekely, J.; Pospíšil, J.; Gates*, K. S. Chem. Res. Tox. 2003, 16, 101.
  1. “Studies on the DNA-damaging properties of the endogenous mutagen fecapentaene-12”
    Szekely, J.; Pospíšil, J.; Gates, K. S. Abstr. Pap. Am. Chem. Soc. 2003, 226, p. 103-TOXI.
  1. “HPLC on chiral nonracemic sorbents with circular dichroism detection: Stereoisomers formed by 1,3-dipolar cycloadditions” Pospíšil, J.; Trávníček, M.; Mannschreck, A.; Potáček*, M. Chem. Listy 2003, 97, 1193-1197.
  1. “Influence of N-substituents of carbamoyl-stabilized azomethine ylides in 1,3-dipolar cycloadditions”
    Pospíšil, J.; Trávníček, M.; Potáček*, M. ARKIVOC 2001, (ii), 146-162.
  1. “Reactions of a new family of amide derivatives of phenanthridinium azomethine ylides with dipolarophiles”
    Trávníček, M.; Pospíšil, J.; Potáček*, M. Collect. Czech. Chem. Commun. 1999, 64, 1993-2006.

Books and book chapters

  1. “Antileishmanial Activity of Lignans, Neolignans, and Other Plant Phenols.” Pospíšil, J.; Konrádová, D.; Strnad, M. In Progress in the Chemistry of Organic Natural Products 115; Springer International Publishing, 2021; pp 115–176. DOI: 10.1007/978-3-030-64853-4_3. 
 
 
  1. “1‐(Phenylsulfonyl)‐3‐oxabicyclo[3.1.0]hexan‐2‐one” Pospíšil, J. “1-(Phenylsulfonyl)-3-oxabicyclo[3.1.0]hexan-2-one” Pospíšil, J. In Encyclopedia of Reagents for Organic Synthesis; Major Reference Works; Wiley Online Library, New Jersey, 2020, pp 1–4. DOI: 10.1002/047084289X.rn02295.
  1. “Julia, Julia-Kocienski, and related sulfur-based alkenylation”
    Markó, I.E.; Pospíšil, J. In Science of Synthesis, Vol. 47a: Alkenes; de Meijere, A., Ed.; Thieme, 2009; p. 105-160.
  1. “The modified Sakurai and related reactions”
    Jacques, T.; Markó, I.E.; Pospíšil, J. In Multicomponent reactions; Zhu, J.; Bienaime, H., Eds.; Wiley, 2005; p. 398-452.