Jacek Młynarski

A. Pieczara, A. Borek-Dorosz, S. Buda, W. Tipping, D. Graham, R. Pawłowski, J. Młynarski, M. Barańska, „Modified glucose as a sensor to track the metabolism of individual living endothelial cells – Observation of the 1602 cm−1 band called “Raman spectroscopic signature of life”” , Biosensors and Bioelectronics

A. Pieczara, E. Matuszyk, P. Szcześniak, J.Młynarski, M. Barańska, „Changes in the mitochondrial membrane potential in endothelial cells can be detected by Raman microscopy”, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy

B. Radwan, S. Rocchetti, E. Matuszyk, M. Sternak, M. Stodulski, R. Pawlowski, J. Młynarski, K. Brzozowski, S. Chlopicki, M. Baranska, „EdU sensing: The Raman way of following endothelial cell proliferation in vitro and ex vivo”, Biosensors and Bioelectronics

K. Molga, S. Szymkuć, P. Gołębiowska, O. Popik, P. Dittwald, M. Moskal, R. Roszak, J. Młynarski, B. Grzybowski, „A computer algorithm to discover iterative sequences of organic reactions”, Nature Synthesis

R. Pawłowski, M. Stodulski, J. Młynarski, „Propargylation of CoQ0 through the Redox Chain Reaction”, J. Org. Chem.

A. Osuch-Kwiatkowska, S. Jarosz, „Synthesis of the precursors of iminosugars with 7-membered ring”, Carbohydrate Research

J. Młynarski, J. A. Jaszczewska-Adamczak, „Asymmetric Epoxidation of Enones Promoted by Dinuclear Magnesium Catalyst”, Adv. Synth. Catal.

R. Campagna, Ł. Mateuszuk, K. Wojnar-Lason, P. Kaczara, A. Tworzydło, A. Kij, R. Bujok, J. Młynarski, Y. Wange, D. Sartini, M. Emanuelli, S. Chlopicki, „Nicotinamide N-methyltransferase in endothelium protects against oxidant stress-induced endothelial injury”, BBA – Molecular Cell Research.

E. Matuszyk, A. Adamczyk, B. Radwan, A. Pieczara, P. Szcześniak, J. Młynarski, K. Kamińska, M. Barańska, „Multiplex Raman imaging of organelles in endothelial cells”, Spectrochim. Acta A Mol. Biomol. Spectrosc.

I. Węglarz, K. Michalak, J. Młynarski, „Zinc‐Catalyzed Asymmetric Hydrosilylation of Cyclic Imines: Synthesis of Chiral 2‐Aryl‐Substituted Pyrrolidines as Pharmaceutical Building Blocks”, Adv. Synth. Catal.

P. Sokołowska, S. Jarosz, „Disaccharides as building blocks for novel glycomacrocycles”, Carbohydrate Chemistry: Chemical and Biological Approaches

Ł. Szyszka, S. Jarosz, „Chiral cyclotriveratrylene-based molecular cages: Synthesis and molecular recognition properties”, Trends in Organic Chemistry

Ł. Szyszka, P. Cmoch, M. Górecki, M. Ceborska, M. Potopnyk, S. Jarosz, „Chiral Molecular Cages Based on Cyclotriveratrylene and Sucrose Units Connected with p-Phenylene Linkers”, Eur. J. Org. Chem.

J. Jaźwiński, P. Łata, K. Tiara, S. Jarosz, „Striking difference in reactivity of trienes and oximes derived from glucose and xylose”, Arkivoc

Ł. Szyszka, M. Górecki, P. Cmoch, S. Jarosz, „Fluorescent Molecular Cages with Sucrose and Cyclotriveratrylene Units for the Selective Recognition of Choline and Acetylcholine”, J. Org. Chem.

P. Sokołowska, K. Dąbrowa, S. Jarosz, „Visible-Light Responsive Sucrose-Containing Macrocyclic Host for Cations”, Org. Lett.

B. Mikulak-Klucznik, P. Gołębiowska, A. A. Bayly, O. Popik, T. Klucznik, S. Szymkuć, E. P. Gajewska, P. Dittwald, O. Staszewska-Krajewska, W. Beker, T. Badowski, K. A. Scheidt, K. Molga, J. Młynarski, M. Mrksich, B. A. Grzybowski, „Computational planning of the synthesis of complex natural products”, Nature

M. Pasternak‐Suder, W. Pacułt, S. Baś, J. Młynarski, „Asymmetric Aldol Reaction of Pyruvate Promoted by Chiral Tertiary Amines”, ChemistrySelect

M. Stefaniak, S. Buda, J. Młynarski, „Asymmetric hetero Diels‐Alder reaction of trans‐1‐methoxy‐3‐trimethylsilyloxy‐buta‐1,3‐diene catalyzed by zinc complexes”, Eur. J. Org. Chem.

A. Świerczek, K. Pociecha, M. Ślusarczyk, G. Chłoń-Rzepa, S. Baś, J. Młynarski, K. Więckowski, M. Zadrożna, B. Nowak, E. Wyska, „Comparative Assessment of the New PDE7 Inhibitor – GRMS-55 and Lisofylline in Animal Models of Immune-Related Disorders: A PK/PD Modeling Approach”, Pharm Res

I. Węglarz, M. Szewczyk, J. Młynarski, „Zinc Acetate Catalyzed Enantioselective Reductive Aldol Reaction of Ketones”, Adv. Synth. Catal.

E. P. Gajewska, S. Szymkuć, P. Dittwald, M. Startek, O. Popik, J. Młynarski, B. A. Grzybowski, „Algorithmic Discovery of Tactical Combinations for Advanced Organic Syntheses”, Chem

M. Nawój, A. Grobelny, J. Młynarski, „Macrolide Core Synthesis of Calysolin IX via Intramolecular Glycosylation Approach”, Eur. J. Org. Chem.

A. Adamkiewicz, I. Węglarz, A. Butkiewicz, M. Woyciechowska, J. Młynarski, „Lewis Acid‐Catalyzed Stereoselective α‐Addition of Chiral Aldehydes to Cyclic Dienol Silanes: Aqueous Synthesis of Chiral Butenolides”, Adv. Synth. Catal.

G. Witkowski, M. Potopnyk, K. Tiara, A. Osuch-Kwiatkowska, S. Jarosz, „Synthesis of Highly Oxygenated Bicyclic Carbasugars. Remarkable Difference in the Reactivity of the d-gluco and d-xylo- Derived Trienes”, Molecules

S. Jarosz, P. Sokołowska, Ł. Szyszka, „Synthesis of fine chemicals with high added value from sucrose: Towards sucrose-based macrocycles”, Tetrahedron Letters

P. Szcześniak, S. Buda, L. Lefevre, O. Staszewska‐Krajewska, J. Młynarski, „Total Asymmetric Synthesis of (+)‐Paroxetine and (+)‐Femoxetine”, Eur. J. Org. Chem.

M. A. Dudek, E. Machalska, T. Oleszkiewicz, E. Grzebelus, R. Baranski, P. Szcześniak, J. Młynarski, G. Zając, A. Kaczor, M. Barańska, „Chiral Amplification in Nature: Cell‐extracted Chiral Carotenoid Microcrystals Studied Via RROA of Model Systems”, Angew. Chem. Int. Ed.

P. Szcześniak, O. Staszewska-Krajewska, J. Młynarski, „Total Asymmetric Synthesis of (+)-Asenapine.”, Org. Biomol. Chem.

Ł. Szyszka, P. Cmoch, A. Butkiewicz, M. Potopnyk, S. Jarosz, „Synthesis of Cyclotriveratrylene-Sucrose-Based Capsules”, Org. Lett.

A. Gajewska, A. Osuch-Kwiatkowska, S. Jarosz, „Synthesis of sulfur containing macrocycles with sucrose scaffold”, Carbohydr. Res.

P. Sokołowska, M. Kowalski, S. Jarosz, „First Synthesis of Cryptands with Sucrose Scaffold, Beilstein”, J. Org. Chem.

S. Jarosz, K. Tiara, M. A. Potopnyk, „Stereoselective synthesis of sugar mimetics from simple monosaccharides”, Pur. Appl. Chem.

F. Stanek, R. Pawłowski, J. Młynarski, M. Stodulski, „Visible‐Light‐Mediated α‐Oxygenation of 3‐(N,N‐Dimethylaminomethyl)‐Indoles to Aldehydes”, Eur. J. Org. Chem.

P. Banachowicz, J. Młynarski, S. Buda, „Intramolecular tandem seleno-Michael/aldol reaction: a simple route to hydroxy cyclo-1-ene-1-carboxylate esters.”, J. Org. Chem.

M. Stefaniak, G. Łopatkiewicz, M. Antkowiak, J. Młynarski, „Stereocontrolled Synthesis of Oleanolic Saponin Ladyginoside A Isolated from Ladyginia Bucharica.”, Carbohydr. Res.

S. Baś, R. Kusy, M. Pasternak-Suder, C. Nicolas, J. Młynarski, O. Martin, „Total Synthesis of Pipecolic Acid and 1-C-Alkyl 1,5-Iminopentitol Derivatives by way of Stereoselective Aldol Reactions from (S)-Isoserinal.”, Org. Biomol. Chem.

K. Tiara, M. A. Potopnyk, S. Jarosz, „Synthesis of sucrose-based macrocycle with unsymmetrical monosaccharides „arms” ” , Beilstein J. Org. Chem.

K. Łęczycka-Wilk, F. Ulatowski, P. Cmoch, S. Jarosz, „ „Choose-a-Size” Control in the Synthesis of Sucrose Based Thiourea Macrocycles”, Org. Biomol. Chem.

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

P. Szcześniak, O. Staszewska-Krajewska, B. Furman, J. Młynarski, „Solid supported Hayashi-Jorgensen Catalyst as an Efficient and Recyclable Catalyst for Asymmetric Michael Addition Reaction”, Tetrahedron: Asymmetry

G. Łopatkiewicz, S. Buda, J. Młynarski, „Application of the EF and GH Fragments to the Synthesis of Idraparinux”, J. Org. Chem.

A. Dudek, J. Młynarski, „Iron-Catalyzed Nitro-Mannich Reaction”, J. Org. Chem.

P. Szcześniak, O. Staszewska-Krajewska, B. Furman, J. Młynarski, „Asymmetric Synthesis of Cyclic Nitrones via Organiocatalytic Michael Addition of Aldehydes to Nitroolefins and Subsequent Reductive Cyclization Chemistry”, Select

P. Konieczny, Ł. Michalski, R. Podgajny, S. Chorazy, R. Pełka, D. Czernia, S. Buda, J. Młynarski, B. Sieklucka, T. Wasiutyński, „Self-Enhancement of Rotating Magnetocaloric Effect in Anisotropic Two-Dimensional (2D) Cyanido-Bridged MnII–NbIV Molecular Ferrimagnet”, Inorg. Chem.

K. Łęczycka-Wilk, K. Dabrowa, P. Cmoch, S. Jarosz, „Chloride-Templated Macrocyclization and Anion-Binding Properties of C2-Symmetric Macrocyclic Ureas Derived from Sucrose”, Org. Lett.

M. Szewczyk, A. Bezłada, J. Mlynarski, „Zinc-Catalyzed Enantioselective Hydrosilylation of Ketones and Imines Under Solvent-Free Conditions”, ChemCatChem

G. Łopatkiewicz, J. Mlynarski, „Synthesis of L-Pyranosides by Hydroboration of Hex-5-enopyranosides Revisited”, J. Org. Chem.

S. Baś, J. Mlynarski, „Synthesis of 2-Keto-D- and L-Gluconic Acid via Stereoselective Direct Aldol Reactions”, J. Org. Chem.

M. A. Molenda, S. Baś, J. Mlynarski, „A Concise Organocatalytic Synthesis of 3-deoxy-2-Ulosonic Acids via Cinchona Alkaloid-Promoted Aldol Reaction of Pyruvate”, Eur. J. Org. Chem.

A. Adamkiewicz, M. Woyciechowska, J. Mlynarski, „a-Regioselective Aqueous Mukaiyama Aldol Reaction of 2-(Trimethylsilyloxy)furan with Pyruvates”, Eur. J. Org. Chem.

G. Zajac, A. Kaczor, A. Pallares Zazo, J. Mlynarski, M. Dudek, M. Baranska, „Aggregation-Induced Resonance Raman Optical Activity (AIRROA) – a New Mechanism for Chirality Enhancement”, J. Phys. Chem. B.

A. Adamkiewicz, J. Mlynarski, „Diastereoselective Hydrosilylation of N-(tert-butanesulfinyl)-imines Catalyzed by Zinc Acetate”, Eur. J. Org. Chem.

A. Bezłada, M. Szewczyk, J. Mlynarski, „Enantioselective Hydrosilylation of Imines Catalyzed by Chiral Zinc Acetate Complexes”, J. Org. Chem.

G. Zajac, A. Kaczor, S. Buda, J. Mlynarski, J. Frelek, J. Dobrowolski, M. Baranska, „Prediction of ROA and ECD Related to Conformational Changes of Astaxantin Enantiomers”, J. Phys. Chem. B.

M. Szewczyk, F. Stanek, A. Bezłada, J. Mlynarski, „Zinc Acetate-Catalyzed Highly Enantioselective Hydrosilylation of Ketones”, Adv. Synth. Catal.

M. Rogozińska-Szymczak, J. Mlynarski, „Unmodified Primary Amine Organocatalysts for Asymmetric Michael Reaction in Aqueous Media”, Eur. J. Org. Chem.

S. Chorazy, M. Reczynski, R. Podgajny, W. Nogas, S. Buda, M. Rams, W. Nitek, B. Nowicka, J. Mlynarski, S.-i. Ohkoshi, B. Sieklucka, „Implementation of Chirality into High-Spin Ferromagnetic CoII9WV6 and NiII9WV6 Cyanido-Bridged Clusters”, Cryst. Growth Des.

B. Gut, J. Mlynarski, „Tertiary Amine-Promoted Asymmetric Aldol Reaction of Aldehydes”, Eur. J. Org. Chem.

S.Chorazy, R. Podgajny, W. Nogas, S. Buda, W. Nitek, J. Mlynarski, M. Rams, M. Kozieł, E. Juszyńska-Gałązka, V. Vieru, L. Chibotaru, B. Sieklucka, „Optical Activity and Dehydration-Driven Switching of Magnetic Properties in Enantiopure Cyanido-Bridged CoII3WV2 Trigonal Bipyramids”, Inorg. Chem.

O. Popik, M. Pasternak-Suder, S. Baś, J. Mlynarski, „Organocatalytic Synthesis of Higher-carbon Sugars: Efficient Protocols for the Synthesis of Natural Seduheptulose and D-glycero-L-galacto-oct-2-ulose”, ChemistryOpen. This article is part of the Virtual Special Issue “Carbohydrates in the 21st Century: Synthesis and Applications”.

M. A. Molenda, S. Baś, O. El-Sepelgy, M. Stefaniak, J. Mlynarski, „Chemistry of Pyruvate Enolates: anti-selective Direct Aldol Reaction of Pyruvate Ester with Chiral Aldehydes Promoted by Dinuclear Zinc Catalyst”, Adv. Synth. Catal.

S. Buda, M. Nawój, P. Gołębiowska, K. Dyduch, A. Michalak, J. Mlynarski, „Application of 2-Substituted Benzyl Groups in Stereoselective Glycosylation”, J. Org. Chem.

D. Łowicki, S. Baś, J. Mlynarski, „Chiral Zinc Catalysts for Asymmetric Synthesis”, Tetrahedron

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