Zespół VIII

E. Chlebus, M. Chlebus, A. Szmurło, K. Dąbrowa, „Is contact allergy to preservatives, antioxidants and fragrances an additional factor influencing the treatment rosacea?”, Dermatol Rev, 2020, 107, 210-227

P. Niedbała, J. Jurczak, „Effective synthetic strategy towards highly selective macrocyclic anion receptors based on static combinatorial chemistry”, Tetrahedron, 2020, 76, 131693

K. Dąbrowa, P. Niedbała, M. Pawlak, M. Lindner, W. Ignacak, Janusz Jurczak, „Tuning Anion-Binding Properties of 22-Membered Unclosed Cryptands by Structural Modification of the Lariat Arm”, ACS Omega, 2020, 5, 29601–29608

M. Majdecki, A. Tyszka-Gumkowska, J. Jurczak, „Highly Enantioselective Epoxidation of α,β-Unsaturated Ketones Using Amide-Based Cinchona Alkaloids as Hybrid Phase-Transfer Catalysts”, Org. Lett., 2020, 22, 8687-8691

J. Cedrowski, K. Dąbrowa, A. Krogul-Sobczak, G. Litwinienko, „A Lesson Learnt from Food Chemistry—Elevated Temperature Triggers the Antioxidant Action of Two Edible Isothiocyanates: Erucin and Sulforaphane”, Antioxidants, 2020, 9, 1090

G. Pikus, A. Tyszka-Gumkowska, J. Jurczak, „Static Combinatorial Chemistry: A High-Pressure Approach to the Synthesis of Macrocyclic Benzoamide Libraries”, ACS Comb. Sci., 2020, 22, 213-221

M. Majdecki, P. Niedbała, J. Jurczak, „Synthesis of C2 Hybrid Amide‐Based PTC Catalysts and Their Comparison with Saturated Analogues”, ChemistrySelect, 2020, 5, 6424-6429

S. Wasiłek, J. Jurczak, „The Impact of Solvent and the Receptor Structure on Chiral Recognition Using Model Acyclic Bisamides Decorated with Glucosamine Pendant Arms”, J. Org. Chem., 2020, 85, 11902-11907

G. Pikus, A. Tyszka-Gumkowska, J. Jurczak, „The influence of high pressure on static combinatorial libraries of chiral BINOL-based macrocyclic amides”, Tetrahedron, 2020, 76, 131438

P. Niedbała, J. Jurczak, „One-Pot Parallel Synthesis of Unclosed Cryptands—Searching for Selective Anion Receptors via Static Combinatorial Chemistry Techniques”, ACS Omega, 2020, 5, 26271-26277

O. Święch, M. Majdecki, L.J. Opuchlik, R. Bilewicz, „Impact of pH and cell medium on the interaction of doxorubicin with lipoic acid cyclodextrin conjugate as the drug carrier”, J. Incl. Phenom. Macrocycl. Chem., 2020, 97, 129-136

O. Święch, A. Krzak, M. Majdecki, A. Trębińska-Stryjewska, M. Wakuła, p. Garbacz, W. Gąsiorowska, R. Bilewicz, „Water-soluble galactosamine derivative of β-cyclodextrin as protective ligand and targeted carrier for delivery of toxic anthracycline drug”, Int. J. Pharm., 2020, 589, 119834

K. Dąbrowa, M. Lindner, S. Wasiłek, J. Jurczak, „Selective Recognition of Chloride by a 24‐Membered Macrocyclic Host with a Hydrophobic Methylenepyrene Substituent”, European Journal of Organic Chemistry, 2020, 2020, 4528-4533

P. Niedbała, M. Majdecki, K. Dąbrowa, J. Jurczak, „Selective Carboxylate Recognition Using Urea-Functionalized Unclosed Cryptands: Mild Synthesis and Complexation Studies”, J. Org. Chem., 2020, 85, 5058–5064

A. Tyszka-Gumkowska, J. Jurczak, „A General Method for High-Pressure-Promoted Postfunctionalization of Unclosed Cryptands: Potential Phase-Transfer Catalysts”, J. Org. Chem., 2019, 85, 1308-1314

M. Majdecki, P. Niedbała, J. Jurczak, „Amide-Based Cinchona Alkaloids as Phase-Transfer Catalysts: Synthesis and Potential Application”, Org. Lett., 2019, 21, 19, 8085-8090.

M. Majdecki, A. Krzak, K. Żelechowska, O. Swiech, „Monosubstituted hydrazone β-cyclodextrin derivatives for pH-sensitive complex formation with aromatic drugs”, J. Incl. Phenom. Macrocycl. Chem., 2019, 93, 77-83.

A. Tyszka, G. Pikus, K.Dabrowa, J. Jurczak, „Late-Stage Functionalization of (R)-BINOL-Based Diazacoronands and Their Chiral Recognition of alpha-Phenylethylamine Hydrochlorides”, J. Org. Chem., 2019, 84, 6502-6507.

A. Tyszka-Gumkowska, G. Pikus, J. Jurczak, „Chiral Recognition of Carboxylate Anions by (R)-BINOL-Based Macrocyclic Receptors”, Molecules, 2019, 24, 2635-2643.

M. Lindner, A. Krasiński, J. Jurczak, „Facile, stereocontrolled synthetic route towards bis-functionalised pyrrolizidines”, Synthesis, 2018, 50, 4295-4300.

J. Grabowski, J.M. Granda, J. Jurczak, „Preparation of acetals from aldehydes and alcohols under basic conditions”, Org. Biomol. Chem., 2018, 16, 3114-3120.

A. Cholewiak, P. Stepniak, J. Jurczak, „Linear neutral receptors for anions: synthesis, structure and applications”, Synthesis, 2018, 50, 4555-4568.

A. Cholewiak, Ł. Dobrzycki, J. Jurczak, F. Ulatowski, „Disulphide bond exchange inhibited by air-kinetic and thermodynamic products in a library of macrocyclic cysteine derivatives”, Org. Biomol. Chem., 2018, 16, 2411-2420.

J. Jurczak, A. Sobczuk, K. Dąbrowa, M. Lindner, P. Niedbała, P. Stepniak, „Chirality of 20-membered unclosed cryptand: macroring distortion via lariat arm modification”, Chirality, 2018, 30, 219-225.

K. Dąbrowa , M. Ceborska, J. Jurczak, „Solid-state entrapment of water clusters by 26-membered pentamide unclosed cryptands–probing the para-substituent effect”, Supramol. Chem., 2018, 30, 464-472.

D. Lichosyt, S. Wasiłek, P. Dydio, J. Jurczak, „The influence of binding site geometry on anion-binding selectivity: a case study of macrocyclic receptors built on the azulene skeleton”, Chem. Eur. J., 2018, 24, 11683-11692.

J. Jurczak, A. Sobczuk, K. Dabrowa, M. Lindner, P. Niedbała, „An indirect synthetic approach toward conformationally constrained 20-membered unclosed cryptands via late-stage installation of intraannular substituents”, J. Org. Chem., 2018, 83, 13560-13567.

K.Dabrowa, F. Ulatowski, D. Lichosyt, J. Jurczak, „Catching the chloride: Searching for non-Hofmeister selectivity behavior in systematically varied polyamide macrocyclic receptors”, Org. Biomol. Chem., 2017, 15 5927-5943.

P. Stepniak, B. Lainer, K. Chmurski, J. Jurczak, „pH-Controlled recognition of amino acids by urea derivatives of β-cyclodextrin”, RSC Adv., 2017, 7 15742-15746.

G. Pikus, E. Paśniczek, J. Jurczak, „The influence of salt additives on macrocyclic product distributions in double-amidation reactions”, Arkivoc, 2017, 534-545.

K. Dabrowa, M. Ceborska, M. Pawlak, J. Jurczak, „Comparative structural studies of four homologous thioamidic unclosed crytpands: Self-encapsulation of lariat arm, odd-even effects, anomalously short ss chalcogen bonding, and more”, Cryst. Growth. Des., 2017, 17, 701-710.

K. Dąbrowa, J. Jurczak, „Tetra-(meta-butylcarbamoyl)azobenzene: A Rationally Designed Photoswitch with Binding Affinity for Oxoanions in a Long-Lived Z-State”, Org. Lett., 2017, 19, 1378-1381.

P. Stepniak, B. Lainer, K. Chmurski, J. Jurczak, „The effect of urea moiety in amino acid binding by β-cyclodextrin derivatives: A 1000-fold increase in efficacy comparing to native β-cyclodextrin”, Carb. Polym., 2017, 164, 233-241.

A. Cholewiak, A. Tycz, J. Jurczak, „8-Propyldithieno[3,2-b:2′,3′-e]pyridine-3,5-diamine (DITIPIRAM) Derivatives as Neutral Receptors Tailored for Binding of Carboxylates”, Org. Lett., 2017, 19, 3001-3004.

F. Ulatowski, J. Jurczak, „Oligocarboxylates as useful templates in dynamic combinatorial chemistry”, Pure Appl. Chem. 2017, 89 801-807.

K. Ziach, J. Jurczak, J. Romański, „Sodium thiocyanate binding by a 3-aminobenzoic acid based ion pair receptor consisting of a thiourea binding domain”, Inorg. Chem. Commun., 2017, 84, 251-254.

A. Krzak, O. Święch, M. Majdecki, R. Bilewicz, „Complexing daunorubicin with β-cyclodextrin derivative increases drug intercalation into DNA”, Electrichim. Acta, 2017, 247, 139-148.

D. Jagleniec, K. Ziach, K. Dąbrowa, J. Romański, „Late-Stage Functionalization of (R)-BINOL-Based Diazacoronands and Their Chiral Recognition of α-Phenylethylamine Hydrochlorides”, J. Org. Chem., 2019, 84, 10, 6502-6507.

D. Jagleniec, K. Ziach, K. Dąbrowa, J. Romański, „The effect of substitution pattern on binding ability in regioisomeric ion pair receptors based on an aminobenzoic platform”, Molecules, 2019, 24, 2990.

Jurczak J., Sobczuk A., Dąbrowa K., Lindner M., Niedbała P., „An Indirect Synthetic Approach toward Conformationally Constrained 20-Membered Unclosed Cryptands via Late-Stage Installation of Intraannular Substituents”, J. Org. Chem. 2018, 83, 13560-13567.

Chaciak B., Dąbrowa K., Świder P., Jarosz S., „Macrocyclic Derivatives with Sucrose Scaffold: Insertion of a Long Polyhydroxylated Linker Between the Terminal 6, 6’-Positions”, New J. Chem., 2018, 42, 18578-18584.

Dąbrowa, K.; Ceborska, M., Jurczak J., „Solid-State Entrapment of Water Clusters by 26-Membered Pentamide Unclosed Cryptands – Probing the para-Substituent Effect”, Supramol. Chem. 2018, 30, 464–472.

Lindler M., Niedbała P., Dabrowa K., Stępniak P. M., Sobczuk A., Jurczak J., „Catching the chloride: searching for non-Hofmeister selectivity behavior in systematically varied polyamide macrocyclic receptors”, Chirality 2018, 30, 219–225.

Dąbrowa K., Ulatowski F., Lichosyt D., Jurczak J., "Efficient nucleophilic substitution in self-assembled monolayer of dithiol on gold Chemistry of Heterocyclic Compounds", Org. Biomol. Chem. 2017, 15, 5927–5943.

Ceborska M., Zimnicka M., Kowalska A. A., Dąbrowa K., Repeć B., "Rotaxanes composed of dibenzo-24-crown-8 and macrocyclic transition metal complexing tetraimine units", Beilstein J. Org. Chem. 2017, 13, 2252–22631

Łęczycka-Wilk K., Dabrowa K., Cmoch P., Jarosz S., "Chloride-Templated Macrocyclization and Anion-Binding Properties of C 2-Symmetric Macrocyclic Ureas from Sucrose", Org. Lett. 2017, 19, 4596–4599.

Dąbrowa K., Jurczak J., "Tetra-(meta-butylcarbamoyl)azobenzene: a rationally designed photoswitch with binding affinity for oxoanions in long-lived Z-state", Org. Lett. 2017, 19, 1378–1381.

Dąbrowa K., Ceborska M., Pawlak M., Jurczak J., "Comparative structural studies of four homologous thioamidic unclosed crytpands: self-encapsulation of lariat arm, odd-even effects, anomalously short S···S chalcogen bonding, and more", Cryst. Growth Des. 2017, 17, 701–710.

Ziach K., Dąbrowa K., Niedbała P., Kalisiak J., Jurczak J., „Exploration of structural motifs influencing solid-state conformation and packing of unclosed cryptands sharing the same 19-membered macrocyclic core”, Tetrahedron 2016, 72, 8373–8381.

Dąbrowa K., Niedbała P., Jurczak J., „Engineering Light-Mediated Bistable Azobenzene Switches Bearing Urea D ‑ Aminoglucose Units for Chiral Discrimination of Carboxylates”, J. Org. Chem. 2016, 81, 3576–3584.

Ulatowski F., Dąbrowa K., Bałakier T., Jurczak J., „Recognizing the Limited Applicability of Job Plots in Studying Host − Guest Interactions in Supramolecular Chemistry”, J. Org. Chem. 2016, 81, 1746–1756.

Ulatowski F., Dąbrowa K., Jurczak J., „Supramolecular detection of geometrical differences of azobenzene carboxylates”, Tetrahedron Lett. 2016, 57, 1820–1824.

Dąbrowa K., Niedbała M., Majdecki P., Duszewski P., Jurczak J., „A General Method for Synthesis of Unclosed Cryptands via H‑Bond Templated Macrocyclization and Subsequent Mild Postfunctionalization”, Org. Lett. 2015, 17, 4774–4777.

Dąbrowa K., Niedbała P., Jurczak J., „Anion-tunable control of thermal Z→E isomerization in basic azobenzene receptors”, Chem. Commun. 2014, 50, 15748–15751.

Dąbrowa K., Ceborska M., Jurczak J., „Trapping of Octameric Water Cluster by the Neutral Unclosed Cryptand Environment”, Cryst. Growth Des. 2014, 14, 4906–4910.

Paluch P., Kaźmierski S., Jeziorna A., Sniechowska J., Dąbrowa K., Panek J. J., Jezierska-Mazzarello A., Jurczak J., Potrzebowski M. J., „Influence of Environmental Humidity on Organization and Molecular Dynamics of Heteromacrocyclic Assemblies”, J. Phys. Chem. B 2013, 117, 14420–14431.

Dąbrowa, K., Pawlak, M., Duszewski, P., Jurczak J., „Unclosed Cryptands”: A Point of Departure for Developing Potent Neutral Anion Receptors”, Org. Lett. 2012, 14, 6298–6301.