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Łukasz Albrecht's Research Group
Łukasz Albrecht
Łukasz Albrecht was born in Łódź, Poland (1980). He obtained his M.Sc. (2004), Ph.D. (2009) and habilitation (2015) from the Lodz University of Technology, Poland. In 2009-2012 he was a postdoctoral fellow with Professor Karl Anker Jørgensen at the Center for Catalysis, Aarhus University, Denmark. Since 2013 he has started his independent research activity at the Lodz University of Technology, Poland working on new applications of asymmetric organocatalysis.
90. The Influence of Experimental Parameters on Quantitative Deuterium Measurements for Ethyl Alcohols of Different Origin. Ciepielowski, G.; Pacholczyk‐Sienicka, B.; Klajman, K.; Paneth, P.; Albrecht, Ł. J. Sci. Food Agric. 2020, 100, 1812–1815.
89. Allylic-Allylic Alkylation with 3,5-Dimethyl-4-Nitroisoxazole: A Route to Dicarboxylic Acid Derivatives. Kowalczyk-Dworak, D.; Kwit, M.; Albrecht, Ł. J. Org. Chem. 2020, 85, 2938–2944.
88. The Game of Electrons: Organocatalytic Higher‐Order Cycloadditions Involving Fulvene‐ and Tropone‐Derived Systems. Frankowski, S.; Romaniszyn, M.; Skrzyńska, A.; Albrecht, Ł. Chem. – A Eur. J. 2020, 26, 2120–2132.
87. Asymmetric Formal Vinylogous Iminium Ion Activation for Vinyl-Substituted Heteroaryl and Aryl Aldehydes. Gao, X. Y.; Yan, R. J.; Xiao, B. X.; Du, W.; Albrecht, Ł.; Chen, Y. C. Org. Lett. 2019, 21, 9628–9632.
86. Site-Selective and Enantioselective α,β,γ-Functionalization of 5-Alkylidenefuran-2(5 H)-Ones: A Route to Polycyclic γ-Lactones. Skrzyńska, A.; Frankowski, S.; Moczulski, M.; Drelich, P.; Albrecht, Ł. Org. Lett. 2019, 21, 1248–1252.
85. α,β-Unsaturated Butenolides in an Organocatalytic Doubly Annulative Cascade for the Preparation of 3,4-Dihydrocoumarins. Kowalczyk-Dworak, D.; Albrecht, L. Org. Biomol. Chem. 2019, 17, 2624–2628.
83. The Role of Saccharomyces Cerevisiae Yeast and Lactic Acid Bacteria in the Formation of 2-Propanol from Acetone during Fermentation of Rye Mashes Obtained Using Thermal-Pressure Method of Starch Liberation. Pielech-Przybylska, K.; Balcerek, M.; Dziekońska-Kubczak, U.; Pacholczyk-Sienicka, B.; Ciepielowski, G.; Albrecht, Ł.; Patelski, P. Molecules 2019, 24, 610–624.
82. 2-Substituted 1,4-Naphthoquinones in [6 + 4]-Cycloaddition with 8,8-Dicyanoheptafulvene. Romaniszyn, M.; Gronowska, K.; Albrecht, Ł. J. Org. Chem. 2019, 84, 9929–9936.
81. Effect of Co-Inoculation with Saccharomyces Cerevisiae and Lactic Acid Bacteria on the Content of Propan-2-Ol, Acetaldehyde and Weak Acids in Fermented Distillery Mashes. Pielech-Przybylska, K.; Balcerek, M.; Ciepielowski, G.; Pacholczyk-Sienicka, B.; Albrecht, Ł.; Dziekońska-Kubczak, U.; Bonikowski, R.; Patelski, P. Int. J. Mol. Sci. 2019, 20, 1659–1675.
80. Aromatizative Inverse-Electron-Demand Hetero-Diels-Alder Reaction in the Synthesis of Benzothiophene Derivatives. Saktura, M.; Joachim, B.; Grzelak, P.; Albrecht, Ł. European J. Org. Chem. 2019, 2019, 6592–6596.
79. Polyphenolic Profiles in Lettuce (Lactuca Sativa L.) after CaCl2 Treatment and Cold Storage. Materska, M.; Olszówka, K.; Chilczuk, B.; Stochmal, A.; Pecio, Ł.; Pacholczyk-Sienicka, B.; Piacente, S.; Pizza, C.; Masullo, M. Eur. Food Res. Technol. 2019, 245, 733–744.
78. Inverting the Reactivity of Troponoid Systems in Enantioselective Higher-Order Cycloaddition. Frankowski, S.; Skrzyńska, A.; Albrecht, Ł. Chem. Commun. 2019, 55, 11675–11678.
76. The First Application of 1H NMR Spectroscopy for the Assessment of the Authenticity of Perfumes. Ciepielowski, G.; Pacholczyk-Sienicka, B.; Albrecht, Ł. Preprints 2019
75. Breaking Aromaticity with Aminocatalysis: A Convenient Strategy for Asymmetric Synthesis Przydacz, A.; Skrzyńska, A.; Albrecht, Ł. Angew. Chem. Int. Ed. 2019, 58, 63–73.
74. Comparison of quantitative NMR and IRMS spectrometry for the authentication of Polish Vodka Ciepielowski, G.; Pacholczyk-Sienicka, B.; Frączek, T.; Klajman, G.; Paneth, P.; Albrecht, Ł. , J. Sci. Food Agric. 2019, 99, 263–268.
73. Synthesis of γ,γ-Disubstituted Butenolides through a Doubly Vinylogous Organocatalytic Cycloaddition Skrzyńska, A.; Drelich, P.; Frankowski, S.; Albrecht, Ł. Chem. Eur. J. 2018, 24, 16543–16547.
72. Enantioselective organocatalytic approach to δ-lactones bearing a fused cyclohexanone scaffold Kowalczyk, D.; Albrecht, Ł. Tetrahedron Lett. 2018, 59, 2636–2639.
71. The Application of 2-Benzyl-1,4-naphthoquinones as Pronucleophiles in Aminocatalytic Synthesis of Tricyclic Derivatives Skrzyńska, A.; Romaniszyn, M.; Pomikło, D.; Albrecht, Ł. J. Org. Chem. 2018, 83, 5019–5026.
70. Isothiocyanate Strategy for the Synthesis of Quaternary Amino Acids Bearing a Spirocyclic Ring System Frankowski, S.; Gajda, T.; Albrecht, Ł. Adv. Synth. Catal. 2018, 360, 1822-1832.
69. Bifunctional catalysis in the stereocontrolled synthesis of tetrahydro-1,2-oxazines Moczulski, M.; Drelich, P.; Albrecht, Ł. Org. Biomol. Chem. 2018, 16, 376-379.
68. Vinylogous Nucleophiles Bearing the Endocyclic Double Bond in the Allylic Alkylation with Morita-Baylis-Hillman Carbonates Kowalczyk, D.; Albrecht, Ł. Adv. Synth. Catal. 2017, DOI: 10.1002/adsc.201701185
67. Brønsted-base-catalyzed Remote Cascade Reactivity of 2,4-Dienones - Asymmetric Synthesis of Tetrahydrothiophenes Przydacz, A.; Kowalczyk, R.; Albrecht, Ł. Org. Biomol. Chem. 2017, DOI: 10.1039/C7OB02397A.
66. The First Organocatalytic, ortho-Regioselective Inverse-electron-demand Hetero-Diels-Alder Reaction Hejmanowska, J.; Jasiński, M.; Wojciechowski, J. Mlostoń, G.; Albrecht, Ł. Chem. Commun. 2017, 53, 11472-11475.
65. Organocatalytic cis-Aziridination of α,β-Unsaturated Aldehydes. A Facile Entry to syn-1,2-Amino alcohols Frankowski, S.; Bojanowski, J.; Saktura, M.; Romaniszyn, M.; Drelich, P.; Albrecht, Ł., Org. Lett. 2017, 19, 5000–5003.
64. An organocatalytic cis-selective approach to bicyclic δ-lactones Kowalczyk, D.; Albrecht, Ł. Org. Biomol. Chem. 2017, 15, 7286–7289.
63. Convenient d0a3 synthon equivalents for the stereocontrolled synthesis of functionalized 1,4-amino alcohol precursors Drelich, P.; Moczulski, M.; Albrecht, Ł. Org. Lett. 2017, 19, 3143–3146.
62. Studies on the Formation of Dienamine and Trienamine Intermediates by 1H NMR Spectroscopy Łągiewka, B.; Albrecht, Ł. Asian J. Org. Chem. 2017, 6, 516–519 (cover paper)
61. Taming of Thioketones –The First Asymmetric thia-Diels-Alder Reaction with Thioketones as Heterodienophiles Hejmanowska, J.; Jasiński, M.; Mlostoń, G.; Albrecht, Ł. Eur. J. Org. Chem. 2017, 5, 950–954.
60. Aryl, Hetaryl, and Ferrocenyl Thioketones as Versatile Building Blocks for Exploration in the Organic Chemistry of Sulfur Mloston, G.; Grzelak, P.; Hamera-Fałdyga, R.; Jasiński, M.; Pipiak, P.; Urbaniak, K.; Albrecht, Ł.; Hejmanowska, J.; Heimgartner, H. Phosphorus, Sulfur Silicon Relat. Elem.2016, 2, 204–211
59. Organocatalytic asymmetric approach to spirocyclic tetrahydrothiophenes containing either a butenolide or an azlactone structural motif Hejmanowska, J.; Albrecht, Ł. ARKIVOC 2016, 225–241.
58. Asymmetric organocatalysis in the synthesis of pyrrolidine derivatives bearing a benzofuran-3(2H)-one scaffold Kowalczyk, D.; Albrecht, Ł. Synthesis 2016, DOI: 10.1055/s-0035-1562483(invited submission).
57. Organocatalytic doubly annulative approach to 3,4-dihydrocoumarins bearing a fused pyrrolidine scaffold Kowalczyk, D.; Albrecht, Ł. J. Org. Chem. 2016, 81, 6800–6807.
56. Asymmetric synthesis of β-amino-α-hydroxyaldehyde derivatives bearing a quaternary stereogenic center Drelich, P.; Skrzyńska, A.; Albrecht, Ł. Eur. J. Org. Chem.2016, 25, 4302–4306.
55. Asymmetric aminocatalysis in the synthesis of δ-lactone derivatives Albrecht, A.; Skrzyńska, A.; Pietrzak, A.; Bojanowski, J.; Albrecht, Ł. Asian J. Org. Chem. 2016, 9, 1115–1119.
54. Enantioselective synthesis of spirocyclic tetrahydrothiophene derivatives bearing a benzofuran-3(2H)-one scaffold. Unusual supramolecular crystal structure with high Z′ Kowalczyk, D.; Wojciechowski, J.; Albrecht, Ł.Tetrahedron Lett. 2016, 57, 2533–2538.
53. Aminocatalytic strategy for the synthesis of optically active benzothiophene derivatives Skrzyńska, A.; Albrecht, A.; Albrecht, Ł. Adv. Synth. Catal. 2016, 358,2838–2844.
52. Assessing the correlation between the degree of disc degeneration on the Pfirrmann scale and the metabolites identified in HR-MAS NMR spectroscopy Radek, M.; Pacholczyk-Sienicka, B.; Jankowski, S.; Albrecht, Ł.; Grodzka, M.; Depta, A.; Radek, A. Magnetic Resonance Imaging 2016, 34, 376.
51. Asymmetric Synthesis of 3,4-Dihydrocoumarins Bearing a α,α-Disubstituted Amino Acid Moiety Hejmanowska, J.; Albrecht, A.; Pięta, J.; Albrecht, Ł. Adv. Synth. Catal.2015, 357, 3843–3848.
50. Organocatalytic nonclassical trienamine activation in the remote alkylation of furan derivatives Skrzyńska, A.; Przydacz, A.; Albrecht, Ł. Org. Lett.2015, 17, 5682–5685.
49. Nucleophilic catalysis in the enantioselective synthesis of α-methylidene-δ-lactones Albrecht, A.; Skrzyńska, A.; Przydacz, A.; Albrecht, Ł. Synlett 2015, 26, 2679–2684 (invited submission).
48. Chiral Iminophosphoranes — An Emerging Class of Superbase Organocatalysts Krawczyk, H.; Dzięgielewski, M.; Deredas, D.; Albrecht, A.; Albrecht, Ł. Chem. Eur. J. 2015,21, 10268–10277 (hot article).
47. An organocatalytic biomimetic approach to α-aminophosphonates Kowalczyk, D.; Albrecht, Ł. Chem. Commun. 2015, 51, 3981–3984 (cover paper).
46. Asymmetric organocatalysis with organophosphorus reagentsDzięgielewski, M.; Pięta, J.; Kamińska, E.; Albrecht, Ł.Eur. J. Org. Chem. 2015, 677–702 (most accessed from 12.2014 to 11.2015).
45. Organocatalytic enantioselective approach to spirocyclic Δβ,γ-butenolides Hejmanowska, J.; Dzięgielewski, M.; Kowalczyk, D.; Albrecht, Ł.Synlett 2014, 25, 2957–2961 (most accessed in 12.2014).
44. A convenient approach to a novel group of quaternary amino acids containing a geminal bisphosphonate moiety Hejmanowska, J.; Dzięgielewski, M.; Kowalczyk, D.; Albrecht, Ł. Synthesis 2014, 46, 3233–3238.
43. Novel organocatalytic activation of unmodified Morita-Baylis-Hillman alcohols for the synthesis of bicyclic α-alkylidene-ketones Stiller, J.; Kowalczyk, D.; Jiang, H.; Jørgensen, K. A.; Albrecht, Ł. Chem. Eur. J. 2014, 20, 13108–13112.
42. Asymmetric formation of bridged benzoxazocines through an organocatalytic multicomponent dienamine-mediated one-pot cascade Ransborg, L. K.; Overgaard, M.; Hejmanowska J.; Barfüsser, S.; Jørgensen, K. A.; Albrecht, Ł. Org. Lett. 2014, 16, 4182–4185.
41. H-Bonding in aminocatalysis: from proline and beyond Albrecht, Ł.; Jiang, H.; Jørgensen, K. A. Chem. Eur. J. 2014, 20, 358–368(cover paper).
40. Beyond classical reactivity patterns: shifting from 1,4- to 1,6-additions in regio- and enantioselective organocatalyzed vinylogous reactions of olefinic lactones with enals and 2,4-dienals Dell´Amico, L.; Albrecht, Ł.; Naicker, T.; Poulsen, P. H.; Jørgensen, K. A. J. Am. Chem. Soc. 2013, 135, 8063–8070.
39. 1,4-Naphthoquinones in H-bond-directed trienamine-mediated strategies Albrecht, Ł.; Udmark, J.; Gómez, C. V.;Jacobsen, C. B.; Jørgensen, K. A. Org. Lett.2013,15,3010–3013.
38. Aminocatalytic remote functionalization strategies Jiang, H.; Albrecht, Ł.; Jørgensen, K. A. Chem. Sci. 2013, 4, 2287–2300 (cover paper).
37. An efficient synthesis of β,γ,γ-trisubstituted α-diethoxyphosphoryl-γ-lactams: A convenient approach to α-methylene-γ-lactams Deredas, D.; Albrecht, Ł.; Krawczyk, H. Tetrahedron Lett.2013, 54, 3088–3090.
36. Stereocontrolled organocatalytic strategy for the synthesis of optically active cis-2,3-disubstituted-2,3-dihydrobenzofurans Christensen, J.; Albrecht, Ł.; Jørgensen, K. A.Chem. Asian J.2013, 8, 648–652.
35. Three-component reaction of 3-(diethoxyphosphoryl)coumarin, enolizable ketones and primary amines: Simple, stereoselective synthesis of benzo[1,3]oxazocine skeletons Deredas, D.; Albrecht, Ł.; Maniukiewicz, W.; Wojciechowski, J.; Wolf,W. M.; Paluch, P.; Janecki, T.;Różalski, M.; Krajewska, U.; Janecka, A.; Krawczyk, H. RSC Adv. 2013,3, 6821–6832.
34. Dienamine-mediated inverse-electron-demand hetero-Diels-Alder reaction by using enantioselective H-bond-directing strategy Albrecht, Ł. Dickmeiss, G.; Weise, C. F.; Rodríguez-Escrich, C.;Jørgensen, K. A Angew. Chem. Int. Ed.2012, 51, 13109–13113(highlighted in Synfacts).
33. Enantioselective formation of substituted 3,4-dihydrocoumarins by a multicatalytic one-pot process Jacobsen, C. B.; Albrecht, Ł.; Udmark, J.; Jørgensen, K. A. Org. Lett.2012, 14, 5526–5529.
32. Enantioselective H-bond-directing approach for trienamine-mediated reactions in asymmetric synthesis Albrecht, Ł.; Cruz Acosta, F.; Fraile, A.; Albrecht, A.; Christensen, J.; Jørgensen, K. A. Angew. Chem. Int. Ed. 2012, 51, 9088–9092 (hot paper in Angew. Chem. Int. Ed., highlighted in Synfacts).
31. Organocatalytic synthesis of optically active heteroaromatic compounds Albrecht, Ł.; Ransborg, L. K.; Jørgensen, K. A. Catal. Sci. Technol. 2012, 2, 1089–1098.
30. Asymmetric organocatalytic formal [2+2]-cycloadditions via bifunctional H-bond directing dienamine catalysis Albrecht, Ł.; Dickmeiss, G.; Cruz Acosta, F.; Rodríguez-Escrich, C.; Davis, R. L.; Jørgensen, K. A. J. Am. Chem. Soc. 2012, 134, 2543–2546.
29. Optically active thiophenes via an organocatalytic one-pot methodology Ransborg, L. K.; Albrecht, Ł.; Weise, C. F.; Bak, J. R.; Jørgensen, K. A. Org. Lett. 2012,14, 724–727.
28. Enantio- and diastereoselective synthesis of β,γ,γ,δ-tetrasubstituted α-methylene-δ-lactones Albrecht, Ł.; Deredas, D.; Wojciechowski, J.; Wolf, W. M.; Krawczyk, H.; Synthesis2012, 247–252.
27. Taming the Friedel-Crafts reaction – organocatalytic approach to optically active 2,3-dihydrobenzofurans Albrecht, Ł.; Ransborg, L. K.; Lauridsen, V.; Overgaard, M.; Zweifel, T.;Jørgensen, K. A. Angew. Chem. Int. Ed. 2011, 50, 12496–12500.
26. Organocatalytic strategies for the construction of optically active imidazoles, oxazoles and thiazoles Albrecht, Ł.; Ransborg, L. K.; Albrecht, A.; Lykke, L.; Jørgensen, K. A. Chem. Eur. J. 2011,17, 13240–13246 (highlighted in Synfacts).
25. The diarylprolinol silyl ether system: a general organocatalyst Jensen, K. L.; Dickmeiss, G.; Jiang, H.; Albrecht, Ł.; Jørgensen, K. A. Acc. Chem. Res. 2012, 45, 248–264.
24. A simple recipe for sophisticated cocktails: organocatalytic one-pot reactions - concept, nomenclature, and future perspectives Albrecht, Ł.; Jiang, H.; Jørgensen, K. A. Angew. Chem. Int. Ed. 2011, 50, 8492–8509.
23. Asymmetric trienamine catalysis for the construction of structurally rigid cyclic α,α-disubstituted amino acid derivatives Jiang, H.; Gschwend, B.; Albrecht, Ł.; Hansen, S. G.; Jørgensen, K. A. Chem. Eur. J. 2011,17, 9032–9036.
22. Recent advances in the synthesis of α-alkylidene-substituted δ-lactones, γ-lactams and δ-lactams Albrecht, A.; Albrecht, Ł.; Janecki, T. Eur J. Org. Chem. 2011, 2747–2766.
21. Asymmetric organocatalytic [3+2]-annulation strategy for the synthesis of N-fused heteroaromatic compounds Albrecht, Ł.; Albrecht, A.; Ransborg, L. K.; Jørgensen, K. A. Chem. Sci. 2011, 2, 1273–1277.
20. An organocatalytic approach to 2-hydroxyalkyl- and 2-aminoalkyl furanes Albrecht, Ł.; Ransborg, L. K.; Gschwend, B.; Jørgensen, K. A. J. Am. Chem. Soc.2010, 132, 17886–17893(highlighted in Synfacts).
19. Organocatalytic preparation of simple β-hydroxy and β-amino esters: low catalyst loadings and gram-scale synthesis Jiang, H.; Gschwend, B.; Albrecht, Ł.; Jørgensen, K. A. Org. Lett.2010, 12, 5052–5055 (highlighted in Synfacts).
18. Asymmetric formal trans-dihydroxylation and trans-aminohydroxylation ofα,β-unsaturated aldehydes via an organocatalytic reaction cascade Albrecht, Ł.; Jiang, H.; Dickmeiss, G.; Gschwend, B.; Hansen, S. G.; Jørgensen, K. A. J. Am. Chem. Soc. 2010, 132, 9188–9196.
17. A convenient synthesis and cytotoxic evaluation of β-aryl-α-methylidene-γ-lactones and β-aryl-α-methylidene-γ-lactams Albrecht, A.; Albrecht, Ł.; Różalski, M.; Krajewska, U.; Janecka, A.; Studzian, K.; Janecki T. New J. Chem. 2010, 34, 750–761.
16. Organocatalytic asymmetric synthesis of organophosphorus compounds Albrecht, Ł.; Albrecht, A.; Krawczyk, H.; Jørgensen, K. A. Chem. Eur. J.2010,16, 28–48.
15. Synthesis and cytotoxic evaluation of β-alkyl or β-aryl-δ-methyl-α-methylene-δ-lactones. Comparison with the corresponding γ-lactones Albrecht, Ł.; Wojciechowski, J.; Albrecht, A.; Wolf, W. M.; Janecka, A.; Studzian, K.; Krajewska, U.; Różalski, M.; Janecki, T.; Krawczyk, H. Eur. J. Med. Chem. 2010, 45, 710–718.
14. Chiralne katalizatory organiczne w asymetrycznej reakcji Michaela Albrecht, Ł.; Krawczyk, H. Wiadomości chemiczne 2009, 63, 391–436.
13. An efficient synthesis of β,γ-disubstituted-α-diethoxyphosphoryl-γ-lactones. A convenient approach to α-methylene-γ-lactones Krawczyk, H.; Albrecht, Ł. Phosphorus, Sulfur, and Silicon 2009,184, 963–978.
12. Organocatalytic domino Michael-Knoevenagel-condensation reaction for the synthesis of optically active 3-diethoxyphosphoryl-2-oxocycloclohex-3-enecarboxylates Albrecht, Ł.; Richter, B.; Vila, C.; Krawczyk, H.; Jørgensen, K. A. Chem. Eur. J. 2009,15, 3093–3102 (cover paper).
11. Rac-(1S,2R)-Diethyl [6-hydroxy-1-(4-methoxyphenyl)-3-oxo-2,3-dihydro-1H-benzo[f]chromen-2-yl]phosphonate Wojciechowski, J.; Krawczyk, H.; Albrecht, Ł.; Wolf, W. M. Acta Cryst. 2008, E64, 1240–1241.
10. Enantioselective organocatalytic approach to α-methylene-δ-lactones and δ-lactams Albrecht, Ł.; Richter, B.; Krawczyk, H.; Jørgensen, K. A. J. Org. Chem. 2008, 73, 8337–8343.
9. A novel and convenient synthesis of cyclopent-1-enecarboxylates by an intramolecular Horner-Wadsworth-Emmons reaction Krawczyk, H.; Albrecht, Ł. Synthesis 2008, 3951–3956.
8. Synthesis and crystal structure of 1-(aminomethyl)vinylphosphonic acid Krawczyk, H.; Albrecht, Ł.; Wojciechowski, J.; Wolf, W.M. Tetrahedron 2008,64, 5051–5054.
7. A convenient synthesis and cytotoxic evaluation of N-unsubstituted α-methylene-γ-lactams Krawczyk, H.; Albrecht, Ł.; Wojciechowski, J.; Wolf, W. M.; Krajewska, U.; Różalski, M. Tetrahedron 2008, 64, 6307–6314
6. Trifluoromethanesulfonic acid mediated Friedel-Crafts reaction of (E)-3-aryl-2-(diethoxyphosphoryl)acrylic acids with electron-rich hydroxyarenes. A convenient approach to α-methylene-δ-valerolactones Krawczyk, H.; Albrecht, Ł.; Wojciechowski, J.; Wolf, W. M. Tetrahedron 2007, 63, 12583–12594.5.
5. Rac-Diethyl [(1S,2R)-1-(4-bromophenyl)-6-hydroxy-3-oxo-2,3-dihydro-1H-benzo[f]chromen-2-yl]phosphonate Krawczyk, H.; Albrecht, Ł.; Wojciechowski, J.; Wolf, W. M. Acta Cryst. 2007, E63, o4148.
4. Bromodecarboxylation of (E)-3-aryl-2-(diethoxyphosphoryl)acrylic acids: A facile route to diethyl arylethynylphosphonates Krawczyk, H.; Albrecht, Ł.Synthesis 2007, 1877–1881.
3. (2R*,3R*,4R*)-tert-Butyl 2-(diethoxyphosphoryl)-4-nitro-3-(4-nitrophenyl) pentanoate Krawczyk, H.; Albrecht, Ł.; Wojciechowski, J.; Wolf, W. M.Acta Cryst. 2006, E62, o2746–o2745.
2. Spontaneous Nef reaction of 3-aryl-2-(diethoxyphophoryl)-4-nitroalkanoic acids Krawczyk, H.; Albrecht, Ł.; Wojciechowski, J.; Wolf, W. M. Tetrahedron 2006, 62,9135–9145.
1. Knoevenagel reaction of diethylphosphonoacetic acid: A facile route to diethyl (E)-2-arylvinylphosphonates Krawczyk, H.; Albrecht, Ł. Synthesis 2005, 2887–2896.
1. Deciphering a synthetic strategy – The art and beauty of organic synthesis
Pięta, J.; Drelich, P.; Przydacz, A.; Albrecht, A.; Albrecht, Ł. In Encyclopedia of Physical Organic Chemistry, 2016, ISBN: 978-1-118-47045-9
2. TMS-Prolinol catalyst in organocatalysis
Jiang, H.; Albrecht, Ł.; Dickmeiss, G.; Jensen, K. L.; Jørgensen, K. A. in Comprehensive Enantioselective Organocatalysis: Catalysts, Reactions, and Applications (Ed. Dalko, P. I.) Wiley-VCH, Weinheim, 2013, 33-50.
3. α-Alkylidene-γ- and δ-lactones and Lactams
Albrecht, Ł.; Albrecht, A.; Janecki, T.; in Natural Lactones and Lactams - Synthesis, Occurrence and Biological Activity(Ed. Janecki, T.) Wiley-VCH, Weinheim, 2013, 147-192.