2023
114. Comparison of Diastereoselective ortho-Metalations and C–H Activations of Chiral Ferrocenes. T. Čarný, R. Šebesta, Synlett 2023, DOI: 10.1055/a-2089-4934.
113. Asymmetric tandem conjugate addition and reaction with carbocations on acylimidazole Michael acceptors. B. Mudráková, R. M. de Figueiredo, J.-M. Campagne, R. Šebesta, Beilstein J. Org. Chem. 2023, 19, 881-888.
112. Enolates ambushed – asymmetric tandem conjugate addition and subsequent enolate trapping with conventional and less traditional electrophiles. P. Kisszékelyi; R. Šebesta, Beilstein J. Org. Chem. 2023, 19, 593–634.
111. Asymmetric organocatalysis under mechanochemical conditions. V. Nemethová, D. Krištofíková, M. Mečiarová, R. Šebesta, Chem. Rec. 2023, e202200283.
110. Mechanochemical Radical Boronation of Aryl Diazonium Salts Promoted by Sodium Chloride. S. Andrejčák, P. Kisszékelyi, M. Májek, R. Šebesta, Eur. J. Org. Chem. 2023, e202201399.
2022
109. Derivatives of benzo-1,4-thiazine-3-carboxylic acid and the corresponding amino acid conjugates. P. Kisszékelyi, T. Peňaška, K. Stankovianska, M. Mečiarová, R. Šebesta, Beilstein J. Org. Chem. 2022, 18, 1195–1202.
108. Mechanochemical Pd-Catalyzed Cross-Coupling of Arylhalides and Organozinc Pivalates. T. Čarný, T. Peňaška, S. Andrejčák, R. Šebesta, Chem. Eur. J. 2022, e202202040.
107. Pro-Pro Dipeptide-Thiourea Organocatalyst in the Mannich Reaction between alpha-Imino Esters and Pyruvates; P. Čmelová, P. Šramel, B. Zahradníková, V. Modrocká, H. Szabados, M. Mečiarová, R. Šebesta, Eur. J. Org. Chem. 2022, e202200106.
106. Asymmetric Tandem Conjugate Addition and Reaction with Carbocations on Unsaturated Heterocycles. B. Mudráková, P. Kisszékelyi, D. Vargová, D. Zakiewicz, R. Šebesta, Adv. Synth. Catal. 2022, 364, 1337-1344.
105. New advances in asymmetric organocatalysis. R. Šebesta, Beilstein J. Org. Chem. 2022, 18, 240-242.
104. Catalyst-Promoted Diastereodivergent Enantioselective Formal oxa-Diels-Alder Reaction of Unsaturated Ketones with Enoates Under Liquid-Assisted Grinding Conditions. T. Peňaška, V. Modrocká, K. Stankovianska, M. Mečiarová, E. Rakovský, R. Šebesta, ChemSusChem 2022, 15, e202200028.
2021
103. N-Sulfinylpyrrolidine-containing ureas and thioureas as bifunctional organocatalysts. V. Poláčková, D. Krištofíková, B. Némethová, R. Górová, M. Mečiarová, R. Šebesta, Beilstein J. Org. Chem. 2021, 17, 2629–2641.
102. Asymmetric Sequential Michael Addition and Cyclization Reactions of 2-(2-Nitrovinyl)phenols Catalyzed by Bifunctional Amino-Squaramides. E. Veverková, P. Molnosiová, R. Šebesta, SynOpen 2021, 5, 278-284.
101. Diastereoselective Double C-H Functionalization of Chiral Ferrocenes with Heteroaromatics. K. Plevová, P. Kisszékelyi, D. Vargová, S. Andrejčák, V. Tóth, L. Fertáľ, E. Rakovský, J. Filo, R. Šebesta, Chem. Eur. J. 2021, 27, 15501-15507.
100. Isomerization of Ferrocenyl Phosphinites to Phosphane-oxides and retro-Phospha-Brook Rearrangement. A. Almássy, A. Hejtmánková, D. Vargová, R. Šebesta, J. Organomet. Chem. 2021, 941, 121801.
99. Stereoselective Organocatalytic Construction of Spiro Oxindole Pyrrolidines Using Unsaturated alpha-Ketoesters and alpha-Ketoamides. T. Peňaška, V. Palchykov, E. Rakovský, G. Addová, R. Šebesta, Eur. J. Org. Chem. 2021, 1693-1703.
98. Hybrid Peptide–Thiourea Catalyst for Asymmetric Michael Additions of Aldehydes to Heterocyclic Nitroalkenes, P. Čmelová, D. Vargová, R. Šebesta, J. Org. Chem. 2021, 86, 581-592.
97. Are Organozirconium Reagents Applicable in Current Organic Synthesis, I. Némethová, R. Šebesta, Synthesis 2021, 53, 447-460.
2020
96. Mechanochemically Activated Asymmetric Organocatalytic Domino Mannich Reaction-Fluorination. D. Krištofíková, M. Mečiarová, E. Rakovský, R. Šebesta, ACS Sust. Chem. Eng. 2020, 8, 14417–14424.
95. Asymmetric copper-catalyzed conjugate additions of organometallic reagents in the syntheses of natural compounds and pharmaceuticals. D. Vargová, I. Némethová, R. Šebesta, Org. Biomol. Chem. 2020, 18, 3780-3796.
94. Synthesis of chiral 3,4-disubstituted pyrrolidines with antibacterial properties. L. Rodriguez, R. Fišera, B. Gaálová, K. Koči, H. Bujdáková, M. Mečiarová, R. Górová, H. Jurdáková, R. Šebesta, Eur. J. Org. Chem. 2020, 2565-2575.
93. Green Asymmetric Organocatalysis. D. Krištofíková, V. Modrocká, M. Mečiarová, R. Šebesta, ChemSusChem 2020, 13, 2828-2858.
92. Reductive alkylation of imines via asymmetric Cu-catalyzed addition of organozirconium reagents. I. Némethová, D. Vargová, B. Mudráková, J. Filo, R. Šebesta, J. Organomet. Chem. 2020, 908, 121099.
2019
91. Why do thioureas and squaramides slow down the Ireland-Claisen rearrangement? D. Krištofíková, J. Filo, M. Mečiarová, R. Šebesta, Beillstein J. Org. Chem. 2019, 15, 2948-2957.
90. Reductions of Imines using zirconocene chloride hydride. D. Vargová, B. Mudráková, I. Némethová, R. Šebesta, Eur. J. Org. Chem. 2019, 7606-7612.
89. Trapping of chiral enolates generated by Lewis acid promoted conjugate addition of Grignard reagents to unreactive Michael acceptors by various electrophiles. D. Vargová, J. M. Perez, S. R. Harutyunyan, R. Šebesta, Chem. Commun. 2019, 55, 11766-11769.
88. Transformation of Racemic Azlactones into Enantioenriched Dihydropyrroles and Lactones Enabled by Hydrogen‐Bond Organocatalysis. M. Žabka, A. Kocian, S. Bilka, S. Andrejčák, R. Šebesta, Eur. J. Org. Chem. 2019, 6077-6085.
87. Bifunctional Thio/Squaramide Catalyzed Stereoselective Michael Additions of Aldehydes to Nitroalkenes towards Synthesis of Chiral Pyrrolidines. K. Ormandyová, S. Bilka, M. Mečiarová, R. Šebesta, ChemistrySelect, 2019, 4, 8870-8875.
86. Diastereoselective Pd-Catalyzed CH Arylation of Ferrocenylmethanamines with Arylboronic Acids or Pinacol Esters. K. Plevová, B. Mudráková, E. Rakovský, R. Šebesta, J. Org. Chem. 2019, 84, 7312-7319.
85. Asymmetric Transition-Metal Catalysis in the Formation and Functionalization of Metal Enolates. D. Vargová, I. Némethová, K. Plevová, R. Šebesta, ACS Catal. 2019, 9, 3104-3143.
84. Copper-Catalyzed Conjugate Addition of in-situ Formed Alkyl Boranes to α,β-Unsaturated Ketones. B. Mravec, K. Plevová, R. Šebesta, Monatsh. Chem. 2019, 150, 295-302.
83. Organocatalysts Effect on the Stereoselectivity of [2,3]-Wittig Rearrangement. T. Peňaška, M. Meyer Mojzes, J. Filo, H. Jurdáková, M. Mečiarová, R. Šebesta, Eur. J. Org. Chem. 2019, 605-610.
2018
82. Bifunctional Amine-Squaramides as Organocatalysts in Michael/hemiketalization Reactions of β,γ-Unsaturated α-Ketoesters and α,β-Unsaturated ketones with 4-Hydroxycoumarins. V. Modrocká, E. Veverková, M. Mečiarová, R. Šebesta, J. Org. Chem. 2018, 83, 13111-13120.
81. Synthesis and structural characterisation of Group 11 metal complexes with a phosphinoferrocene oxazoline. O. Bárta, M. Drusan, I. Císařová, R. Šebesta, P. Štěpnička, New J. Chem. 2018, 42, 11450-11457.
80. Investigations towards the stereoselective organocatalyzed Michael addition of dimethyl malonate to a racemic nitroalkene: possible route to the 4-methylpregabalin core structure. D. Vargová, R. Baran, R. Šebesta, Beilstein J. Org. Chem. 2018, 14, 553-559.
79. Enantioselective Synthesis of 2,3-Dihydrofurocoumarins by Squaramide-Catalyzed Michael Addition/Cyclization of 4-Hydroxycoumarins with b-Nitrostyrenes. V. Modrocká, E. Veverková, R. Baran, R. Šebesta, ChemistrySelect 2018, 3, 1466-1471.
78. Enantioselective copper-catalyzed conjugate additions of in situ generated organozirconium reagents to N-heterocyclic Michael acceptors. I. Némethová, S. Bilka, R. Šebesta, J. Organomet. Chem. 2018, 856, 100-108.
77. Peptide-catalyzed stereoselective Michael addition of aldehydes and ketones to heterocyclic nitroalkenes. V. Poláčková, P. Čmelová, R. Górová, R. Šebesta, Monatsh. Chem. 2018, 149, 729-736.
76. A practical three-step synthesis of vinylferrocene. K. Plevová, B. Mudráková, R. Šebesta, Synthesis 2018, 50, 760-763.
75. Synthesis of sulfone analog of oseltamivir precursor. V. Poláčková, R. Šándrik, R. Šebesta, Chem. Pap. 2018, 72, 221-227.
2017
74. Organocatalytic Diastereoselective Synthesis of Spirooxindols via [3+2] Cycloadditions of Azomethine Ylides with α,β-Unsaturated Esters. T. Peňaška, K. Ormandyová, M. Mečiarová, J. Filo, R. Šebesta, New J. Chem. 2017, 41, 5506-5512.
73. Electrophilic trapping of zirconium enolates obtained by Cu-catalyzed addition of in-situ generated organozirconium reagents. I. Némethová, Z. Sorádová, R. Šebesta, Synthesis, 2017, 49, 2461-2469.
72. Stereoisomers of oseltamivir – synthesis, in silico prediction and biological evaluation.
V. Hajzer, R. Fišera, A. Latika, J. Durmis, J. Kollár, V. Frecer, Z. Tučeková, S. Miertuš, F. Kostolanský, E. Varečková, R. Šebesta, Org. Biomol. Chem. 2017, 15, 1828-1841.
71. Organocatalyst efficiency in α-aminoxylation and α-hydrazination of carbonyl derivatives in aqueous media and ball-mill. E. Veverková, V. Modrocká, R Šebesta, Eur. J. Org. Chem. 2017, 1191-1195.
70. Fe–Li Interactions in Ferrocenyllithium Compounds, A. Malastová, J. Vallo, A. Almássy, M. Pitoňák, P. Neogrády, R. Šebesta, Eur. J. Inorg. Chem. 2017, 483-488.
2016
69. Enantioselective organocatalysis using SOMO activation. M. Meciarova, P. Tisovský, R. Sebesta New J. Chem. 2016, 40, 4855-4864.
68. Enantioselective Cu-Catalyzed Functionalizations of Unactivated Alkenes. Z. Soradová, R. Šebesta, ChemCatChem 2016, 8, 2581-2588.
67. Squaramide-Catalyzed Michael Addition as a Key Step for the Direct Synthesis of GABAergic Drugs
E. Veverková, S. Bilka, R. Baran, R. Šebesta Synthesis, 2016, 48, 1474-1482.
66. Synthesis of epimer of Taniaphos ligand. A. Almássy, E. Rakovský, A. Malastová, Z. Soradová, R. Šebesta, J. Organomet. Chem. 2016, 805, 130-138.
2015
65. Enantioselective Michael Reaction of Acetals with Nitroalkenes: An Improvement of the Oseltamivir Synthesis. P. Tisovsky, T. Penaska, M. Meciarova, R. Sebesta, ACS Sust. Chem. Eng. 2015, 3, 3429-3434.
64. Experimental and Theoretical Studies in Hydrogen-Bonding Organocatalysis. M. Žabka, R. Šebesta, Molecules 2015, 20(9), 15500-15524.
63. Retro-Brook Rearrangement of Ferrocene-Derivated silyl ethers. V. Bariak, A. Malastová, A. Almássy, R. Šebesta, Chem. Eur. J. 2015, 21, 13445-13453.
62. Optimization of stereoselective Michael addition of 2-(pentan-3-yloxy)acetaldehyde to N-[(Z)-2-nitroethenyl]acetamide with the aid of design of experiments. V. Hajzer, P. Alexy, A. Latika, J. Durmis, R. Šebesta; Monatsh. Chem. 2015, 146, 1541-1545.
61. Applications of Ferrocenium Salts in Organic Synthesis. Š. Toma, R. Šebesta, Synthesis, 2015, 47, 1683-1695.
60. Asymmetric one-pot conjugate addition of Grignard reagents to α,β-unsaturated compounds followed by reaction with carbenium ions. M. Drusan, E. Rakovský, J. Marek, R. Šebesta, Adv. Synth. Catal. 2015, 357, 1493-1498.
59. Assessment of non-standard reaction conditions for asymmetric 1,3-dipolar organocatalytic cycloaddition of nitrone with α,β-unsaturated aldehydes. M. Mojzesová, M. Mečiarová, A. Almássy, R. Marti, R. Šebesta, Chem. Pap. 2015, 69, 737-746.
58. Stereoselective domino conjugate addition of Grignard reagents to lactones followed by reaction with activated alkenes catalyzed by ferrocenyl carbene ligands. Z. Sorádová, J. Máziková, M. Mečiarová, R. Šebesta, Tetrahedron: Asymmetry, 2015, 26, 271-275. (Highlighted in Synfacts, 11, 2015.)
57. Enantioselective Addition of Oxazolones to N-Protected Imines Catalysed by Chiral Thioureas. M. Žabka, A. Malastová, R. Šebesta, RSC Adv. 2015, 5, 12890-12893.
56. Organocatalytic oxa-Diels-Alder reaction of α,ß-unsaturated ketones under non-classical conditions. M. Mojzesová, M. Mečiarová, R. Marti, R. Šebesta, New J. Chem. 2015, 39, 2573 - 2579.
2014
55. Bioactive Carbocyclic Nucleoside Analogues - Syntheses and Properties of Entecavir. M. Campian, M. Putala, R. Šebesta, Curr. Org. Chem. 2014, 18, 2808-2832.
54. Asymmetric organocatalytic SOMO reactions of enol silanes and silyl ketene (thio)acetals. P.Tisovský, M. Mečiarová, R. Šebesta, Org. Biomol. Chem. 2014, 12, 9446-9452.
53. Ferrocene phosphane-heteroatom/carbon bidentate ligands in asymmetric catalysis. Š. Toma, J. Csizmadiová, M. Mečiarová, R. Šebesta, Dalton Trans. 2014, 43, 16557-16579.
52. Organocatalytic SOMO reactions of copper(I)-acetylide and alkylindium compounds with aldehydes. P. Tisovský, M. Mečiarová, R. Šebesta, Chem. Pap. 2014, 68, 1113-1120.
51. Enantioselective Michael additions of aldehydes to nitroalkenes catalyzed with ionically tagged organocatalyst. R. Šebesta, A. Latika, Centr. Eur. J. Chem. 2014, 12, 416-425.
50. Higher enantioselectivities in thiourea-catalyzed Michael additions under solvent-free Conditions. R. Šebesta, M. Hestericová, Tetrahedron, 2014, 70, 901-905.
49. Enantioselective C-C and C-heteroatom bond forming reactions using chiral ferrocene Catalysts. M. Drusan, R. Šebesta, Tetrahedron, 2014, 70, 759-786.
48. Computational study of diastereoselective ortho-lithiations of chiral ferrocenes. A. Škvorcová, R. Šebesta, Org. Biomol. Chem. 2014, 12, 132-140.
2013
47. Enantioselective Michael addition of 1,3-dicarbonyl compounds to nitroalkene catalyzed by chiral squaramides – a key step in the synthesis of pregabalin. R. Baran, E. Veverková, A. Škvorcová, R. Šebesta, Org. Biomol. Chem. 2013, 11, 7705-7711.
46. Diastereoselective copper-catalysed 1,4-addition of Grignard reagents to N-enoyl oxazolidinones. M. Drusan, Z. Galeštoková, R. Šebesta, RSC Adv. 2013, 3, 9881-9888.
45. Asymmetric Mannich reactions catalyzed by proline and 4-hydroxyproline derived organocatalysts in the presence of water. E. Veverková, L. Liptáková, M. Veverka, R. Šebesta, Tetrahedron: Asymmetry 2013, 24, 548-552.
44. Ferrocene phosphane-carbene ligands in Cu-catalyzed enantioselective 1,4-additions of Grignard reagents to α,β-unsaturated carbonyl compounds. J. Csizmadiová, M. Mečiarová, A. Almássy, B. Horváth, R. Šebesta, J. Organomet. Chem. 2013, 737, 47-52.
43. Asymmetric copper-catalyzed 1,4-additions and allylic substitutions with nucleophiles formed by hydrometallation of alkenes. R. Šebesta, ChemCatChem 2013, 5, 1069-1071.(highlight).
42. Explanation of Different Regioselectivities in the ortho-Lithiation of Ferrocenyl(phenyl)methanamines. A. Almássy, A. Škvorcová, B. Horváth, F. Bilčík, V. Bariak, E. Rakovský, R. Šebesta. Eur. J. Org. Chem. 2013, 111-116.
41. Methyltrioxorhenium-catalyzed oxidation of secondary amines to nitrones in ionic liquids. M. Mečiarová, M. Mojzesová, R. Šebesta, Chem. Pap. 2013, 67, 51-58.
2012
40. Enantioselective Michael Addition of the 2-(1-Ethylpropoxy)acetaldehyde to N-[(1Z)-2-Nitroethenyl]acetamide – Optimization of the Key Step in the Organocatalytic Oseltamivir Synthesis. V. Hajzer, A. Latika, J. Durmis, R. Šebesta, Helv. Chim. Acta 2012, 95, 2421-2428.
39. Domino Reactions Initiated by Enantioselective Cu-Catalyzed Conjugate Addition. Z. Galeštoková, R. Šebesta, Eur. J. Org. Chem. 2012, 6688–6695.
38. TADDOL-Based Phosphane–Phosphite Ligands in Enantioselective Cu-Catalyzed Grignard 1,4-Additions Followed by Mannich-Type Alkylations. M. Drusan, W. Loelsberg, A. Škvorcová, H.-G. Schmalz, R. Šebesta, Eur. J. Org. Chem. 2012, 6285-6290.(Highlighted in Synfacts, 9, 2013.)
37. Thiol-Free Synthesis of Oseltamivir and Its Analogues via Organocatalytic Michael Additions of Oxyacetaldehydes to 2-Acylaminonitroalkenes. J. Rehák, M. Huťka, A. Latika, H. Brath, A. Almássy, V. Hajzer, J. Durmis, Š. Toma, R. Šebesta, Synthesis, 2012, 44, 2424-2430.
36. Organocatalyst Efficiency in the Michael Additions of Aldehydes to Nitroalkenes in Water and in a Ball-Mill. E. Veverková, V. Poláčková, L. Liptáková, E. Kázmerová, M. Mečiarová, Š. Toma, R. Šebesta, ChemCatChem 2012, 4, 1013-1018.
35. Enantioselective one-pot conjugate addition of Grignard reagents to cyclic enones followed by amidomethylation. Bilčík, F.; Drusan, M.; Marák, J.; Šebesta, R.; J. Org. Chem. 2012, 77, 760-765.
2011
34. Diastereoselective Mannich Reaction of Chiral Enolates Formed by Enantioselective Conjugate Addition of Grignard Reagents. Galeštoková, Z.; Šebesta, R. Eur. J. Org. Chem. 2011, 7092-7096.
33. [5]Ferrocenophane alkene-phosphane ligands for enantioselective Rh-catalyzed conjugate additions. Csizmadiová, J.; Mečiarová, M.; Rakovský, E.; Horváth, B.; Šebesta, R. Eur. J. Org. Chem. 2011, 6110-6116.
32. Organocatalitic Reactions Under Unusual Conditions. Toma, Š.; Šebesta, R.; Mečiarová, M. Curr. Org. Chem., 2011, 15, 2257-2281.
31. Diastereoselective ortho-lithiation of [5]ferrocenophanes. Škvorcová, A.; Rakovský, E.; Kožíšek, J.; Šebesta, R. J. Organomet. Chem. 2011, 696, 2600-2606.
30. Synthesis of aryl(ferrocenyl)methanols via an enantioselective addition of arylboronic acids. Tisovský, P.; Mečiarová, M.; Šebesta, R. Tetrahedron: Asymmetry 2011, 22, 536-540.
29. Pd–catalyzed conjugate addition of arylboronic acids to α,β-unsaturated ketones under microwave irradiation. Poláčková, V.; Bariak, V.; Šebesta, R.; Toma, Š. Chem. Pap. 2011, 65, 338-344.
2010
28. Enantioselective organocatalytic Michael additions of oxyacetaldehydes to nitroolefins. Huťka, M.; Poláčková, V.; Marák, J.; Kanianský, D.; Šebesta, R.; Toma, Š. Eur. J. Org. Chem. 2010, 6430-6435.
27. Enantioselective one-pot conjugate addition of Grignard reagents followed by Mannich reaction. Šebesta, R.; Bilčík, F.; Fodran, P. Eur. J. Org. Chem. 2010, 5666-5671.
26. Asymmetric allylic substitutions on symmetrical and non-symmetrical substrates using [5]ferrocenophane ligands. Šebesta, R.; Škvorcová, A.; Horváth, B. Tetrahedron: Asymmetry 2010, 21, 1910-1915.
25. Asymmetric Mannich reaction catalyzed by N-arylsulfonyl-L-proline amides. Veverková, E.; Štrasserová, J.; Šebesta, R.; Toma, Š. Tetrahedron: Asymmetry 2010, 21, 58-61.
2009
24. Asymmetric organocatalyzed Michael addition of aldehydes to β-nitrostyrene in ionic liquids. Mečiarová, M.; Toma, Š.; Šebesta, R. Tetrahedron: Asymmetry 2009, 20, 2403-2406.
23. Imidazolium-tagged ferrocenyl diphosphanes in allylic substitution with heteroatom nucleophiles. Šebesta, R.; Bilčík, F. Tetrahedron: Asymmetry 2009, 20, 1892-1896.
22. Influence of structural changes in ferrocene phosphane aminophosphane ligands on their catalytic activity. Šebesta, R.; Škvorcová, A. J. Organomet.Chem. 2009, 694, 1898-1902.
21. Are Ionic Liquids Suitable Media for Organocatalytic Reactions? Toma, Š.; Mečiarová, M.; Šebesta, R. Eur. J. Org. Chem. 2009, 321-327.
2003 – 2008
20. [3] Ferrocenophane ligands with inserted methylene group. Šebesta, R.; Bilčík, F.; Horváth, B. Eur. J. Org. Chem. 2008, 5157-5161.
19. Enantioselective reductions of [m]ferrocenophanones. Šebesta, R.; Mečiarová, M.; Molnár, E.; Cziszmadiová, J.; Fodran, P.; Onomura, O.; Toma, Š. J. Organomet. Chem. 2008, 693, 3131-3134.
18. Benzyl Isopropoxymethyl Carbamate – An Aminomethylating Reagent For Mannich Reactions of Titanium Enolates. Meyer, H.; Beck, A. K.; Šebesta, R.; Seebach, D. Org. Synth. 2008, 85, 287-294.
17. Catalysts with ionic tags and their use in ionic liquids. Šebesta, R.; Kmentová, I.; Toma, Š. Green Chem. 2008, 10, 484-496.
16. [5]Ferrocenophane based ligands for stereoselective Rh-catalyzed hydrogenation and Cu-catalyzed Michael addition. Almássy, A.; Barta, K.; Franciò, G.; Šebesta, R.; Leitner, W.; Toma, Š. Tetrahedron: Asymmetry 2007, 18, 1893-1898.
15. Copper-Catalyzed Enantioselective Conjugate Addition of Organometallic Reagents to Acyclic Dienones. Šebesta, R.; Pizzuti, M. G.; Minnaard, A. J.; Feringa, B. L. Adv. Synth. Catal. 2007, 349, 1931-1937.
14. Imidazolium-Tagged Ferrocene Ligands. Šebesta, R.; Mečiarová, M.; Poláčková, V.; Veverková, E.; Kmentová, I.; Gajdošíková, E.; Cvengroš, J.; Buffa, R.; Gajda, V. Collect. Czech. Chem. Commun. 2007, 72, 1057-1068.
13. New [5]ferrocenophane diphosphine ligands for Pd-catalyzed allylic substitution. Šebesta, R.; Almassy, A.; Císařová, I.; Toma, Š. Tetrahedron: Asymmetry 2006, 17, 2531-2537.
12. Synthesis, and helix or hairpin-turn secondary structures of 'mixed' α/β-peptides consisting of residues with proteinogenic side chains and of 2-amino-2-methylpropanoic acid (Aib). Seebach, D.; Jaun, B.; Sebesta, R.; Mathad, R.I.; Flögel, O.; Limbach, M.; Sellner, H.; Cottens, S. Helv. Chim. Acta 2006, 89, 1801-1825.
11. The Proteolytic Stability of Designed β-Peptides Containing α-Peptide-Bond Mimics and of Mixed α,β-Peptides: Application to the Construction of MHC-Binding Peptides. Hook, D. F.; Bindschädler, P.; Mahajan, Y. R.; Sebesta, R.; Kast, P.; Seebach, D. Chem. Biodiv. 2005, 2, 591.
10. Catalytic enantioselective conjugate addition of dialkylzinc reagents to N-substituted-2,3-dehydro-4-piperidones. Šebesta, R.; Pizzuti, M. G.; Boersma, A. J. ; Minnaard, A. J. ; Feringa, B. L. Chem. Commun. 2005, 1711.
9. How we drifted into peptide chemistry and where we have arrived at. Seebach, D.; Kimmerlin, T.; Šebesta, R.; Campo, M. A.; Beck, A. K. Tetrahedron 2004, 60, 7455.
8. Preparation of (S,S)-Fmoc- β 2hIle-OH, (S)-Fmoc- β 2hMet-OH, and (S)-Fmoc- β 2hTyr(tBu)-OH for Solid-Phase Syntheses of β 2- and β 2/ β 3-Peptides. Sebesta, R.; Seebach, D. Helv. Chim. Acta 2003, 86, 4061.
7. Enantioselective Preparation of 2-Aminomethyl Carboxylic Acid Derivatives: Solving the β2-Amino Acid Problem with the Chiral Auxiliary 4-Isopropyl-5,5-diphenyloxazolidin-2-one (DIOZ). Seebach, D.; Schaeffer, L.; Gessier, F.; Bindschadler, P.; Jager, C.; Josien, D.; Kopp, S.; Lelais, G.; Mahajan, Y. R.; Micuch, P.; Šebesta, P.; Schweizer, B.W. Helv. Chim. Acta 2003, 86, 1582.
Master and PhD-thesis
6. Derivatives of (S)-2-methoxymethylpyrrolidin-1-yl)methylferrocene – new planar chiral ligands. Šebesta, R.; Sališová, M. Collect. Czech. Chem. Commun. 2002, 67, 1700-1708.
5. Cyclodextrins and Their Complexes – Structure and Interactions. Mikuš, P.; Kaniansky, D.; Šebesta, R.; Sališová, M. Chem. Listy 2002, 96, 693. (in Slovak language)
4. Synthesis of (Rp)-2-Aminomethyl-1-[(S)-4-isopropyl-2-yl]ferrocenes. Šebesta, R.; Toma, Š.; Sališová, M. Eur. J. Org. Chem. 2002, 692.
3. Novel Ferrocene Chiral Imines. Šebesta, R.; Sališová, M. Chem. Pap. 2001, 55, 297.
2. Analytical Characterization of Purities of Alkyl- and Arylamino Derivatives of β -Cyclodextrin by Capillary Zone Electrophoresis with Conductivity Detection. Mikuš, P.; Kaniansky, D.; Šebesta, R.; Sališová, M. Enantiomer 1999, 4, 249.
1. Synthesis of New Aminoderivatives of β-Cyclodextrin. Šebesta, R.; Sališová, M. Enantiomer 1999, 4, 271.
114. Comparison of Diastereoselective ortho-Metalations and C–H Activations of Chiral Ferrocenes. T. Čarný, R. Šebesta, Synlett 2023, DOI: 10.1055/a-2089-4934.
113. Asymmetric tandem conjugate addition and reaction with carbocations on acylimidazole Michael acceptors. B. Mudráková, R. M. de Figueiredo, J.-M. Campagne, R. Šebesta, Beilstein J. Org. Chem. 2023, 19, 881-888.
112. Enolates ambushed – asymmetric tandem conjugate addition and subsequent enolate trapping with conventional and less traditional electrophiles. P. Kisszékelyi; R. Šebesta, Beilstein J. Org. Chem. 2023, 19, 593–634.
111. Asymmetric organocatalysis under mechanochemical conditions. V. Nemethová, D. Krištofíková, M. Mečiarová, R. Šebesta, Chem. Rec. 2023, e202200283.
110. Mechanochemical Radical Boronation of Aryl Diazonium Salts Promoted by Sodium Chloride. S. Andrejčák, P. Kisszékelyi, M. Májek, R. Šebesta, Eur. J. Org. Chem. 2023, e202201399.
2022
109. Derivatives of benzo-1,4-thiazine-3-carboxylic acid and the corresponding amino acid conjugates. P. Kisszékelyi, T. Peňaška, K. Stankovianska, M. Mečiarová, R. Šebesta, Beilstein J. Org. Chem. 2022, 18, 1195–1202.
108. Mechanochemical Pd-Catalyzed Cross-Coupling of Arylhalides and Organozinc Pivalates. T. Čarný, T. Peňaška, S. Andrejčák, R. Šebesta, Chem. Eur. J. 2022, e202202040.
107. Pro-Pro Dipeptide-Thiourea Organocatalyst in the Mannich Reaction between alpha-Imino Esters and Pyruvates; P. Čmelová, P. Šramel, B. Zahradníková, V. Modrocká, H. Szabados, M. Mečiarová, R. Šebesta, Eur. J. Org. Chem. 2022, e202200106.
106. Asymmetric Tandem Conjugate Addition and Reaction with Carbocations on Unsaturated Heterocycles. B. Mudráková, P. Kisszékelyi, D. Vargová, D. Zakiewicz, R. Šebesta, Adv. Synth. Catal. 2022, 364, 1337-1344.
105. New advances in asymmetric organocatalysis. R. Šebesta, Beilstein J. Org. Chem. 2022, 18, 240-242.
104. Catalyst-Promoted Diastereodivergent Enantioselective Formal oxa-Diels-Alder Reaction of Unsaturated Ketones with Enoates Under Liquid-Assisted Grinding Conditions. T. Peňaška, V. Modrocká, K. Stankovianska, M. Mečiarová, E. Rakovský, R. Šebesta, ChemSusChem 2022, 15, e202200028.
2021
103. N-Sulfinylpyrrolidine-containing ureas and thioureas as bifunctional organocatalysts. V. Poláčková, D. Krištofíková, B. Némethová, R. Górová, M. Mečiarová, R. Šebesta, Beilstein J. Org. Chem. 2021, 17, 2629–2641.
102. Asymmetric Sequential Michael Addition and Cyclization Reactions of 2-(2-Nitrovinyl)phenols Catalyzed by Bifunctional Amino-Squaramides. E. Veverková, P. Molnosiová, R. Šebesta, SynOpen 2021, 5, 278-284.
101. Diastereoselective Double C-H Functionalization of Chiral Ferrocenes with Heteroaromatics. K. Plevová, P. Kisszékelyi, D. Vargová, S. Andrejčák, V. Tóth, L. Fertáľ, E. Rakovský, J. Filo, R. Šebesta, Chem. Eur. J. 2021, 27, 15501-15507.
100. Isomerization of Ferrocenyl Phosphinites to Phosphane-oxides and retro-Phospha-Brook Rearrangement. A. Almássy, A. Hejtmánková, D. Vargová, R. Šebesta, J. Organomet. Chem. 2021, 941, 121801.
99. Stereoselective Organocatalytic Construction of Spiro Oxindole Pyrrolidines Using Unsaturated alpha-Ketoesters and alpha-Ketoamides. T. Peňaška, V. Palchykov, E. Rakovský, G. Addová, R. Šebesta, Eur. J. Org. Chem. 2021, 1693-1703.
98. Hybrid Peptide–Thiourea Catalyst for Asymmetric Michael Additions of Aldehydes to Heterocyclic Nitroalkenes, P. Čmelová, D. Vargová, R. Šebesta, J. Org. Chem. 2021, 86, 581-592.
97. Are Organozirconium Reagents Applicable in Current Organic Synthesis, I. Némethová, R. Šebesta, Synthesis 2021, 53, 447-460.
2020
96. Mechanochemically Activated Asymmetric Organocatalytic Domino Mannich Reaction-Fluorination. D. Krištofíková, M. Mečiarová, E. Rakovský, R. Šebesta, ACS Sust. Chem. Eng. 2020, 8, 14417–14424.
95. Asymmetric copper-catalyzed conjugate additions of organometallic reagents in the syntheses of natural compounds and pharmaceuticals. D. Vargová, I. Némethová, R. Šebesta, Org. Biomol. Chem. 2020, 18, 3780-3796.
94. Synthesis of chiral 3,4-disubstituted pyrrolidines with antibacterial properties. L. Rodriguez, R. Fišera, B. Gaálová, K. Koči, H. Bujdáková, M. Mečiarová, R. Górová, H. Jurdáková, R. Šebesta, Eur. J. Org. Chem. 2020, 2565-2575.
93. Green Asymmetric Organocatalysis. D. Krištofíková, V. Modrocká, M. Mečiarová, R. Šebesta, ChemSusChem 2020, 13, 2828-2858.
92. Reductive alkylation of imines via asymmetric Cu-catalyzed addition of organozirconium reagents. I. Némethová, D. Vargová, B. Mudráková, J. Filo, R. Šebesta, J. Organomet. Chem. 2020, 908, 121099.
2019
91. Why do thioureas and squaramides slow down the Ireland-Claisen rearrangement? D. Krištofíková, J. Filo, M. Mečiarová, R. Šebesta, Beillstein J. Org. Chem. 2019, 15, 2948-2957.
90. Reductions of Imines using zirconocene chloride hydride. D. Vargová, B. Mudráková, I. Némethová, R. Šebesta, Eur. J. Org. Chem. 2019, 7606-7612.
89. Trapping of chiral enolates generated by Lewis acid promoted conjugate addition of Grignard reagents to unreactive Michael acceptors by various electrophiles. D. Vargová, J. M. Perez, S. R. Harutyunyan, R. Šebesta, Chem. Commun. 2019, 55, 11766-11769.
88. Transformation of Racemic Azlactones into Enantioenriched Dihydropyrroles and Lactones Enabled by Hydrogen‐Bond Organocatalysis. M. Žabka, A. Kocian, S. Bilka, S. Andrejčák, R. Šebesta, Eur. J. Org. Chem. 2019, 6077-6085.
87. Bifunctional Thio/Squaramide Catalyzed Stereoselective Michael Additions of Aldehydes to Nitroalkenes towards Synthesis of Chiral Pyrrolidines. K. Ormandyová, S. Bilka, M. Mečiarová, R. Šebesta, ChemistrySelect, 2019, 4, 8870-8875.
86. Diastereoselective Pd-Catalyzed CH Arylation of Ferrocenylmethanamines with Arylboronic Acids or Pinacol Esters. K. Plevová, B. Mudráková, E. Rakovský, R. Šebesta, J. Org. Chem. 2019, 84, 7312-7319.
85. Asymmetric Transition-Metal Catalysis in the Formation and Functionalization of Metal Enolates. D. Vargová, I. Némethová, K. Plevová, R. Šebesta, ACS Catal. 2019, 9, 3104-3143.
84. Copper-Catalyzed Conjugate Addition of in-situ Formed Alkyl Boranes to α,β-Unsaturated Ketones. B. Mravec, K. Plevová, R. Šebesta, Monatsh. Chem. 2019, 150, 295-302.
83. Organocatalysts Effect on the Stereoselectivity of [2,3]-Wittig Rearrangement. T. Peňaška, M. Meyer Mojzes, J. Filo, H. Jurdáková, M. Mečiarová, R. Šebesta, Eur. J. Org. Chem. 2019, 605-610.
2018
82. Bifunctional Amine-Squaramides as Organocatalysts in Michael/hemiketalization Reactions of β,γ-Unsaturated α-Ketoesters and α,β-Unsaturated ketones with 4-Hydroxycoumarins. V. Modrocká, E. Veverková, M. Mečiarová, R. Šebesta, J. Org. Chem. 2018, 83, 13111-13120.
81. Synthesis and structural characterisation of Group 11 metal complexes with a phosphinoferrocene oxazoline. O. Bárta, M. Drusan, I. Císařová, R. Šebesta, P. Štěpnička, New J. Chem. 2018, 42, 11450-11457.
80. Investigations towards the stereoselective organocatalyzed Michael addition of dimethyl malonate to a racemic nitroalkene: possible route to the 4-methylpregabalin core structure. D. Vargová, R. Baran, R. Šebesta, Beilstein J. Org. Chem. 2018, 14, 553-559.
79. Enantioselective Synthesis of 2,3-Dihydrofurocoumarins by Squaramide-Catalyzed Michael Addition/Cyclization of 4-Hydroxycoumarins with b-Nitrostyrenes. V. Modrocká, E. Veverková, R. Baran, R. Šebesta, ChemistrySelect 2018, 3, 1466-1471.
78. Enantioselective copper-catalyzed conjugate additions of in situ generated organozirconium reagents to N-heterocyclic Michael acceptors. I. Némethová, S. Bilka, R. Šebesta, J. Organomet. Chem. 2018, 856, 100-108.
77. Peptide-catalyzed stereoselective Michael addition of aldehydes and ketones to heterocyclic nitroalkenes. V. Poláčková, P. Čmelová, R. Górová, R. Šebesta, Monatsh. Chem. 2018, 149, 729-736.
76. A practical three-step synthesis of vinylferrocene. K. Plevová, B. Mudráková, R. Šebesta, Synthesis 2018, 50, 760-763.
75. Synthesis of sulfone analog of oseltamivir precursor. V. Poláčková, R. Šándrik, R. Šebesta, Chem. Pap. 2018, 72, 221-227.
2017
74. Organocatalytic Diastereoselective Synthesis of Spirooxindols via [3+2] Cycloadditions of Azomethine Ylides with α,β-Unsaturated Esters. T. Peňaška, K. Ormandyová, M. Mečiarová, J. Filo, R. Šebesta, New J. Chem. 2017, 41, 5506-5512.
73. Electrophilic trapping of zirconium enolates obtained by Cu-catalyzed addition of in-situ generated organozirconium reagents. I. Némethová, Z. Sorádová, R. Šebesta, Synthesis, 2017, 49, 2461-2469.
72. Stereoisomers of oseltamivir – synthesis, in silico prediction and biological evaluation.
V. Hajzer, R. Fišera, A. Latika, J. Durmis, J. Kollár, V. Frecer, Z. Tučeková, S. Miertuš, F. Kostolanský, E. Varečková, R. Šebesta, Org. Biomol. Chem. 2017, 15, 1828-1841.
71. Organocatalyst efficiency in α-aminoxylation and α-hydrazination of carbonyl derivatives in aqueous media and ball-mill. E. Veverková, V. Modrocká, R Šebesta, Eur. J. Org. Chem. 2017, 1191-1195.
70. Fe–Li Interactions in Ferrocenyllithium Compounds, A. Malastová, J. Vallo, A. Almássy, M. Pitoňák, P. Neogrády, R. Šebesta, Eur. J. Inorg. Chem. 2017, 483-488.
2016
69. Enantioselective organocatalysis using SOMO activation. M. Meciarova, P. Tisovský, R. Sebesta New J. Chem. 2016, 40, 4855-4864.
68. Enantioselective Cu-Catalyzed Functionalizations of Unactivated Alkenes. Z. Soradová, R. Šebesta, ChemCatChem 2016, 8, 2581-2588.
67. Squaramide-Catalyzed Michael Addition as a Key Step for the Direct Synthesis of GABAergic Drugs
E. Veverková, S. Bilka, R. Baran, R. Šebesta Synthesis, 2016, 48, 1474-1482.
66. Synthesis of epimer of Taniaphos ligand. A. Almássy, E. Rakovský, A. Malastová, Z. Soradová, R. Šebesta, J. Organomet. Chem. 2016, 805, 130-138.
2015
65. Enantioselective Michael Reaction of Acetals with Nitroalkenes: An Improvement of the Oseltamivir Synthesis. P. Tisovsky, T. Penaska, M. Meciarova, R. Sebesta, ACS Sust. Chem. Eng. 2015, 3, 3429-3434.
64. Experimental and Theoretical Studies in Hydrogen-Bonding Organocatalysis. M. Žabka, R. Šebesta, Molecules 2015, 20(9), 15500-15524.
63. Retro-Brook Rearrangement of Ferrocene-Derivated silyl ethers. V. Bariak, A. Malastová, A. Almássy, R. Šebesta, Chem. Eur. J. 2015, 21, 13445-13453.
62. Optimization of stereoselective Michael addition of 2-(pentan-3-yloxy)acetaldehyde to N-[(Z)-2-nitroethenyl]acetamide with the aid of design of experiments. V. Hajzer, P. Alexy, A. Latika, J. Durmis, R. Šebesta; Monatsh. Chem. 2015, 146, 1541-1545.
61. Applications of Ferrocenium Salts in Organic Synthesis. Š. Toma, R. Šebesta, Synthesis, 2015, 47, 1683-1695.
60. Asymmetric one-pot conjugate addition of Grignard reagents to α,β-unsaturated compounds followed by reaction with carbenium ions. M. Drusan, E. Rakovský, J. Marek, R. Šebesta, Adv. Synth. Catal. 2015, 357, 1493-1498.
59. Assessment of non-standard reaction conditions for asymmetric 1,3-dipolar organocatalytic cycloaddition of nitrone with α,β-unsaturated aldehydes. M. Mojzesová, M. Mečiarová, A. Almássy, R. Marti, R. Šebesta, Chem. Pap. 2015, 69, 737-746.
58. Stereoselective domino conjugate addition of Grignard reagents to lactones followed by reaction with activated alkenes catalyzed by ferrocenyl carbene ligands. Z. Sorádová, J. Máziková, M. Mečiarová, R. Šebesta, Tetrahedron: Asymmetry, 2015, 26, 271-275. (Highlighted in Synfacts, 11, 2015.)
57. Enantioselective Addition of Oxazolones to N-Protected Imines Catalysed by Chiral Thioureas. M. Žabka, A. Malastová, R. Šebesta, RSC Adv. 2015, 5, 12890-12893.
56. Organocatalytic oxa-Diels-Alder reaction of α,ß-unsaturated ketones under non-classical conditions. M. Mojzesová, M. Mečiarová, R. Marti, R. Šebesta, New J. Chem. 2015, 39, 2573 - 2579.
2014
55. Bioactive Carbocyclic Nucleoside Analogues - Syntheses and Properties of Entecavir. M. Campian, M. Putala, R. Šebesta, Curr. Org. Chem. 2014, 18, 2808-2832.
54. Asymmetric organocatalytic SOMO reactions of enol silanes and silyl ketene (thio)acetals. P.Tisovský, M. Mečiarová, R. Šebesta, Org. Biomol. Chem. 2014, 12, 9446-9452.
53. Ferrocene phosphane-heteroatom/carbon bidentate ligands in asymmetric catalysis. Š. Toma, J. Csizmadiová, M. Mečiarová, R. Šebesta, Dalton Trans. 2014, 43, 16557-16579.
52. Organocatalytic SOMO reactions of copper(I)-acetylide and alkylindium compounds with aldehydes. P. Tisovský, M. Mečiarová, R. Šebesta, Chem. Pap. 2014, 68, 1113-1120.
51. Enantioselective Michael additions of aldehydes to nitroalkenes catalyzed with ionically tagged organocatalyst. R. Šebesta, A. Latika, Centr. Eur. J. Chem. 2014, 12, 416-425.
50. Higher enantioselectivities in thiourea-catalyzed Michael additions under solvent-free Conditions. R. Šebesta, M. Hestericová, Tetrahedron, 2014, 70, 901-905.
49. Enantioselective C-C and C-heteroatom bond forming reactions using chiral ferrocene Catalysts. M. Drusan, R. Šebesta, Tetrahedron, 2014, 70, 759-786.
48. Computational study of diastereoselective ortho-lithiations of chiral ferrocenes. A. Škvorcová, R. Šebesta, Org. Biomol. Chem. 2014, 12, 132-140.
2013
47. Enantioselective Michael addition of 1,3-dicarbonyl compounds to nitroalkene catalyzed by chiral squaramides – a key step in the synthesis of pregabalin. R. Baran, E. Veverková, A. Škvorcová, R. Šebesta, Org. Biomol. Chem. 2013, 11, 7705-7711.
46. Diastereoselective copper-catalysed 1,4-addition of Grignard reagents to N-enoyl oxazolidinones. M. Drusan, Z. Galeštoková, R. Šebesta, RSC Adv. 2013, 3, 9881-9888.
45. Asymmetric Mannich reactions catalyzed by proline and 4-hydroxyproline derived organocatalysts in the presence of water. E. Veverková, L. Liptáková, M. Veverka, R. Šebesta, Tetrahedron: Asymmetry 2013, 24, 548-552.
44. Ferrocene phosphane-carbene ligands in Cu-catalyzed enantioselective 1,4-additions of Grignard reagents to α,β-unsaturated carbonyl compounds. J. Csizmadiová, M. Mečiarová, A. Almássy, B. Horváth, R. Šebesta, J. Organomet. Chem. 2013, 737, 47-52.
43. Asymmetric copper-catalyzed 1,4-additions and allylic substitutions with nucleophiles formed by hydrometallation of alkenes. R. Šebesta, ChemCatChem 2013, 5, 1069-1071.(highlight).
42. Explanation of Different Regioselectivities in the ortho-Lithiation of Ferrocenyl(phenyl)methanamines. A. Almássy, A. Škvorcová, B. Horváth, F. Bilčík, V. Bariak, E. Rakovský, R. Šebesta. Eur. J. Org. Chem. 2013, 111-116.
41. Methyltrioxorhenium-catalyzed oxidation of secondary amines to nitrones in ionic liquids. M. Mečiarová, M. Mojzesová, R. Šebesta, Chem. Pap. 2013, 67, 51-58.
2012
40. Enantioselective Michael Addition of the 2-(1-Ethylpropoxy)acetaldehyde to N-[(1Z)-2-Nitroethenyl]acetamide – Optimization of the Key Step in the Organocatalytic Oseltamivir Synthesis. V. Hajzer, A. Latika, J. Durmis, R. Šebesta, Helv. Chim. Acta 2012, 95, 2421-2428.
39. Domino Reactions Initiated by Enantioselective Cu-Catalyzed Conjugate Addition. Z. Galeštoková, R. Šebesta, Eur. J. Org. Chem. 2012, 6688–6695.
38. TADDOL-Based Phosphane–Phosphite Ligands in Enantioselective Cu-Catalyzed Grignard 1,4-Additions Followed by Mannich-Type Alkylations. M. Drusan, W. Loelsberg, A. Škvorcová, H.-G. Schmalz, R. Šebesta, Eur. J. Org. Chem. 2012, 6285-6290.(Highlighted in Synfacts, 9, 2013.)
37. Thiol-Free Synthesis of Oseltamivir and Its Analogues via Organocatalytic Michael Additions of Oxyacetaldehydes to 2-Acylaminonitroalkenes. J. Rehák, M. Huťka, A. Latika, H. Brath, A. Almássy, V. Hajzer, J. Durmis, Š. Toma, R. Šebesta, Synthesis, 2012, 44, 2424-2430.
36. Organocatalyst Efficiency in the Michael Additions of Aldehydes to Nitroalkenes in Water and in a Ball-Mill. E. Veverková, V. Poláčková, L. Liptáková, E. Kázmerová, M. Mečiarová, Š. Toma, R. Šebesta, ChemCatChem 2012, 4, 1013-1018.
35. Enantioselective one-pot conjugate addition of Grignard reagents to cyclic enones followed by amidomethylation. Bilčík, F.; Drusan, M.; Marák, J.; Šebesta, R.; J. Org. Chem. 2012, 77, 760-765.
2011
34. Diastereoselective Mannich Reaction of Chiral Enolates Formed by Enantioselective Conjugate Addition of Grignard Reagents. Galeštoková, Z.; Šebesta, R. Eur. J. Org. Chem. 2011, 7092-7096.
33. [5]Ferrocenophane alkene-phosphane ligands for enantioselective Rh-catalyzed conjugate additions. Csizmadiová, J.; Mečiarová, M.; Rakovský, E.; Horváth, B.; Šebesta, R. Eur. J. Org. Chem. 2011, 6110-6116.
32. Organocatalitic Reactions Under Unusual Conditions. Toma, Š.; Šebesta, R.; Mečiarová, M. Curr. Org. Chem., 2011, 15, 2257-2281.
31. Diastereoselective ortho-lithiation of [5]ferrocenophanes. Škvorcová, A.; Rakovský, E.; Kožíšek, J.; Šebesta, R. J. Organomet. Chem. 2011, 696, 2600-2606.
30. Synthesis of aryl(ferrocenyl)methanols via an enantioselective addition of arylboronic acids. Tisovský, P.; Mečiarová, M.; Šebesta, R. Tetrahedron: Asymmetry 2011, 22, 536-540.
29. Pd–catalyzed conjugate addition of arylboronic acids to α,β-unsaturated ketones under microwave irradiation. Poláčková, V.; Bariak, V.; Šebesta, R.; Toma, Š. Chem. Pap. 2011, 65, 338-344.
2010
28. Enantioselective organocatalytic Michael additions of oxyacetaldehydes to nitroolefins. Huťka, M.; Poláčková, V.; Marák, J.; Kanianský, D.; Šebesta, R.; Toma, Š. Eur. J. Org. Chem. 2010, 6430-6435.
27. Enantioselective one-pot conjugate addition of Grignard reagents followed by Mannich reaction. Šebesta, R.; Bilčík, F.; Fodran, P. Eur. J. Org. Chem. 2010, 5666-5671.
26. Asymmetric allylic substitutions on symmetrical and non-symmetrical substrates using [5]ferrocenophane ligands. Šebesta, R.; Škvorcová, A.; Horváth, B. Tetrahedron: Asymmetry 2010, 21, 1910-1915.
25. Asymmetric Mannich reaction catalyzed by N-arylsulfonyl-L-proline amides. Veverková, E.; Štrasserová, J.; Šebesta, R.; Toma, Š. Tetrahedron: Asymmetry 2010, 21, 58-61.
2009
24. Asymmetric organocatalyzed Michael addition of aldehydes to β-nitrostyrene in ionic liquids. Mečiarová, M.; Toma, Š.; Šebesta, R. Tetrahedron: Asymmetry 2009, 20, 2403-2406.
23. Imidazolium-tagged ferrocenyl diphosphanes in allylic substitution with heteroatom nucleophiles. Šebesta, R.; Bilčík, F. Tetrahedron: Asymmetry 2009, 20, 1892-1896.
22. Influence of structural changes in ferrocene phosphane aminophosphane ligands on their catalytic activity. Šebesta, R.; Škvorcová, A. J. Organomet.Chem. 2009, 694, 1898-1902.
21. Are Ionic Liquids Suitable Media for Organocatalytic Reactions? Toma, Š.; Mečiarová, M.; Šebesta, R. Eur. J. Org. Chem. 2009, 321-327.
2003 – 2008
20. [3] Ferrocenophane ligands with inserted methylene group. Šebesta, R.; Bilčík, F.; Horváth, B. Eur. J. Org. Chem. 2008, 5157-5161.
19. Enantioselective reductions of [m]ferrocenophanones. Šebesta, R.; Mečiarová, M.; Molnár, E.; Cziszmadiová, J.; Fodran, P.; Onomura, O.; Toma, Š. J. Organomet. Chem. 2008, 693, 3131-3134.
18. Benzyl Isopropoxymethyl Carbamate – An Aminomethylating Reagent For Mannich Reactions of Titanium Enolates. Meyer, H.; Beck, A. K.; Šebesta, R.; Seebach, D. Org. Synth. 2008, 85, 287-294.
17. Catalysts with ionic tags and their use in ionic liquids. Šebesta, R.; Kmentová, I.; Toma, Š. Green Chem. 2008, 10, 484-496.
16. [5]Ferrocenophane based ligands for stereoselective Rh-catalyzed hydrogenation and Cu-catalyzed Michael addition. Almássy, A.; Barta, K.; Franciò, G.; Šebesta, R.; Leitner, W.; Toma, Š. Tetrahedron: Asymmetry 2007, 18, 1893-1898.
15. Copper-Catalyzed Enantioselective Conjugate Addition of Organometallic Reagents to Acyclic Dienones. Šebesta, R.; Pizzuti, M. G.; Minnaard, A. J.; Feringa, B. L. Adv. Synth. Catal. 2007, 349, 1931-1937.
14. Imidazolium-Tagged Ferrocene Ligands. Šebesta, R.; Mečiarová, M.; Poláčková, V.; Veverková, E.; Kmentová, I.; Gajdošíková, E.; Cvengroš, J.; Buffa, R.; Gajda, V. Collect. Czech. Chem. Commun. 2007, 72, 1057-1068.
13. New [5]ferrocenophane diphosphine ligands for Pd-catalyzed allylic substitution. Šebesta, R.; Almassy, A.; Císařová, I.; Toma, Š. Tetrahedron: Asymmetry 2006, 17, 2531-2537.
12. Synthesis, and helix or hairpin-turn secondary structures of 'mixed' α/β-peptides consisting of residues with proteinogenic side chains and of 2-amino-2-methylpropanoic acid (Aib). Seebach, D.; Jaun, B.; Sebesta, R.; Mathad, R.I.; Flögel, O.; Limbach, M.; Sellner, H.; Cottens, S. Helv. Chim. Acta 2006, 89, 1801-1825.
11. The Proteolytic Stability of Designed β-Peptides Containing α-Peptide-Bond Mimics and of Mixed α,β-Peptides: Application to the Construction of MHC-Binding Peptides. Hook, D. F.; Bindschädler, P.; Mahajan, Y. R.; Sebesta, R.; Kast, P.; Seebach, D. Chem. Biodiv. 2005, 2, 591.
10. Catalytic enantioselective conjugate addition of dialkylzinc reagents to N-substituted-2,3-dehydro-4-piperidones. Šebesta, R.; Pizzuti, M. G.; Boersma, A. J. ; Minnaard, A. J. ; Feringa, B. L. Chem. Commun. 2005, 1711.
9. How we drifted into peptide chemistry and where we have arrived at. Seebach, D.; Kimmerlin, T.; Šebesta, R.; Campo, M. A.; Beck, A. K. Tetrahedron 2004, 60, 7455.
8. Preparation of (S,S)-Fmoc- β 2hIle-OH, (S)-Fmoc- β 2hMet-OH, and (S)-Fmoc- β 2hTyr(tBu)-OH for Solid-Phase Syntheses of β 2- and β 2/ β 3-Peptides. Sebesta, R.; Seebach, D. Helv. Chim. Acta 2003, 86, 4061.
7. Enantioselective Preparation of 2-Aminomethyl Carboxylic Acid Derivatives: Solving the β2-Amino Acid Problem with the Chiral Auxiliary 4-Isopropyl-5,5-diphenyloxazolidin-2-one (DIOZ). Seebach, D.; Schaeffer, L.; Gessier, F.; Bindschadler, P.; Jager, C.; Josien, D.; Kopp, S.; Lelais, G.; Mahajan, Y. R.; Micuch, P.; Šebesta, P.; Schweizer, B.W. Helv. Chim. Acta 2003, 86, 1582.
Master and PhD-thesis
6. Derivatives of (S)-2-methoxymethylpyrrolidin-1-yl)methylferrocene – new planar chiral ligands. Šebesta, R.; Sališová, M. Collect. Czech. Chem. Commun. 2002, 67, 1700-1708.
5. Cyclodextrins and Their Complexes – Structure and Interactions. Mikuš, P.; Kaniansky, D.; Šebesta, R.; Sališová, M. Chem. Listy 2002, 96, 693. (in Slovak language)
4. Synthesis of (Rp)-2-Aminomethyl-1-[(S)-4-isopropyl-2-yl]ferrocenes. Šebesta, R.; Toma, Š.; Sališová, M. Eur. J. Org. Chem. 2002, 692.
3. Novel Ferrocene Chiral Imines. Šebesta, R.; Sališová, M. Chem. Pap. 2001, 55, 297.
2. Analytical Characterization of Purities of Alkyl- and Arylamino Derivatives of β -Cyclodextrin by Capillary Zone Electrophoresis with Conductivity Detection. Mikuš, P.; Kaniansky, D.; Šebesta, R.; Sališová, M. Enantiomer 1999, 4, 249.
1. Synthesis of New Aminoderivatives of β-Cyclodextrin. Šebesta, R.; Sališová, M. Enantiomer 1999, 4, 271.
Books chapters
1. β 2-Amino acids with proteinogenic side chains and corresponding peptides: synthesis, secondary structure and biological activity. Campo, M. A.; Escalante, J.; Šebesta, R. in Enantioselective Synthesis of β -Amino Acids, 2nd Edition, Eds. Juaristi, E.; Soloshonok, V. A.; VCH Wiley, New York, 2005, pp. 593-617.
2. Ionically-tagged Transition Metal Catalysts. R. Šebesta, in Enantioselective Homogeneous Supported Catalysis, The Royal Society of Chemistry, 2012, pp. 1-17.
3. Enantioselective Homogeneous Supported Catalysis. R. Šebesta, Ed., The Royal Society of Chemistry, 2012.
4. Ionic Liquids as (Co-)solvents and Catalysts for Organocatalytic Reactions. Š. Toma, R. Šebesta in Ionic Liquids in Biotransformations and Organocatalysis: Solvents and Beyond; P. Domínguez de María, Ed., Wiley, Weinheim, 2012.
5. Prolinol Silyl Ethers as Asymmetric Organocatalysts. R. Šebesta, Z. Sorádová in Sustainable Catalysis: Without Metals or Other Endangered Elements, The Royal Society of Chemistry, Part 1, 2015, 166-199, DOI:10.1039/9781782622093-00166