37. "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, accepted; DOI: 10.1021/acs.joc.9b02932.

36. "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.

35. "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.

34. "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.

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

33. "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.

32. "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.

31. "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.

30. "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.

29. "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.

28. “A convenient method for the preparation of 20-[18O]-labeled ingenol
Pospíšil*, J.; Béres, T.; Strnad, M. Tetrahedron Lett. 2017, 58, 1421-1424.

27. “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.

26. “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.

25. “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.

24. “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.

23. “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.

22. “Simple protocol for enhanced (E)-selectivity in Julia-Kocienski reaction
Pospíšil*, J. Tetrahedron Lett. 2011, 52, 2348-2352.

21. “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

20. “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.

19. “Total Synthesis of the Aspercyclides
Pospíšil, J.; Müller, C.; Fürstner*, A. Chem. Eur. J. 2009, 15, 5956-5968.

As PhD student

18. “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.

17. “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.

16. “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 JACSb

15. “Efficient and stereoselective synthesis of allylic ethers and alcohols
Pospíšil, J.; Markó*, I. E. Org. Lett. 2006, 8, 5983-5986.

14. “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

13. “Highly DiastereoselectiveSilyl-Modified Sakurai Multicomponent Reaction
Pospíšil, J.; Kumamoto, T.; Markó*, I. E. Angew. Chem. Int. Ed. 2006, 45, 3357 –3360.

12. “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.

11. “Tetracarbonylhydridoferrate Salts: NaHFe(CO)4 and KHFe(CO)4
Pospíšil*, J. Synlett, 2005, 2543-2544.

10. “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 Ms student

9. “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.

8. “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.

7. “A solvent-free method for substituted imidazolidin- 4-ones synthesis
Pospíšil, J.; Potáček*, M. Heterocycles 2004, 63, 1165-1173.

6. “Microwave-assisted solvent-free synthesis of hexahydrochromeno-[4,3-b] pyrroles
Pospíšil, J.; Potáček*, M. Eur. J. Org. Chem. 2004, 2004, 710-716.

5. “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.

4. “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.

3. “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.

2. “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

2.  “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.