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Natalia Prusinowska

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The Journal of Organic Chemistry|December 8, 2022
Unravelling Structural Dynamics, Supramolecular Behavior, and Chiroptical Properties of Enantiomerically Pure Macrocyclic Tertiary Ureas and ThioureasNatalia Prusinowska, Joanna Szymkowiak, Marcin Kwit
The Journal of Organic Chemistry|January 10, 2018
Enantiopure Tertiary Urea and Thiourea Derivatives of Trianglamine Macrocycle: Structural Studies and Metallogeling PropertiesNatalia Prusinowska, Joanna Szymkowiak, Marcin Kwit
Scientific Reports|May 12, 2026
From triangles to squares - chiral, overcrowded polyimine macrocycles of significant chiroptical response enable the capture of chlorinated solventsNatalia Prusinowska, Agnieszka Czapik, Marcin Kwit
The Journal of Organic Chemistry|April 28, 2021
Chiral Triphenylacetic Acid Esters: Residual Stereoisomerism and Solid-State Variability of Molecular ArchitecturesNatalia Prusinowska, Agnieszka Czapik, Marcin Kwit
Acta Crystallographica. Section B, Structural Science|November 25, 2010
Solid solution of two diastereomers of [3a(R,S),7a(R,S)]-3-[(1'R)-1-phenylethyl]perhydro-1,3-benzothiazol-2-iminium chlorideAgnieszka Plutecka, Urszula Rychlewska, Natalia Prusinowska, et al.
Scientific Reports|January 6, 2025
Thio-modified trianglimines, a novel group of chiral macrocyclic compounds of high structural dynamicsNatalia Prusinowska, Agnieszka Czapik, Joanna Szymkowiak, et al.
Organic & Biomolecular Chemistry|August 13, 2019
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureasNatalia Prusinowska, Agnieszka Czapik, Martika Wojciechowska, et al.
Organic & Biomolecular Chemistry|August 31, 2022
Symmetry-driven diastereoselective functionalization of simple trianglaminePaweł Skowronek, Natalia Prusinowska, Mateusz Bardziński, et al.
Chemistry, an Asian Journal|June 29, 2018
Sterically Crowded Trianglimines-Synthesis, Structure, Solid-State Self-Assembly, and Unexpected Chiroptical PropertiesNatalia Prusinowska, Mateusz Bardziński, Agnieszka Janiak, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
The Journal of Organic Chemistry|December 8, 2022
Unravelling Structural Dynamics, Supramolecular Behavior, and Chiroptical Properties of Enantiomerically Pure Macrocyclic Tertiary Ureas and ThioureasNatalia Prusinowska, Joanna Szymkowiak, Marcin Kwit
The Journal of Organic Chemistry|January 10, 2018
Enantiopure Tertiary Urea and Thiourea Derivatives of Trianglamine Macrocycle: Structural Studies and Metallogeling PropertiesNatalia Prusinowska, Joanna Szymkowiak, Marcin Kwit
Scientific Reports|May 12, 2026
From triangles to squares - chiral, overcrowded polyimine macrocycles of significant chiroptical response enable the capture of chlorinated solventsNatalia Prusinowska, Agnieszka Czapik, Marcin Kwit
The Journal of Organic Chemistry|April 28, 2021
Chiral Triphenylacetic Acid Esters: Residual Stereoisomerism and Solid-State Variability of Molecular ArchitecturesNatalia Prusinowska, Agnieszka Czapik, Marcin Kwit
Acta Crystallographica. Section B, Structural Science|November 25, 2010
Solid solution of two diastereomers of [3a(R,S),7a(R,S)]-3-[(1'R)-1-phenylethyl]perhydro-1,3-benzothiazol-2-iminium chlorideAgnieszka Plutecka, Urszula Rychlewska, Natalia Prusinowska, et al.
Scientific Reports|January 6, 2025
Thio-modified trianglimines, a novel group of chiral macrocyclic compounds of high structural dynamicsNatalia Prusinowska, Agnieszka Czapik, Joanna Szymkowiak, et al.
Organic & Biomolecular Chemistry|August 13, 2019
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureasNatalia Prusinowska, Agnieszka Czapik, Martika Wojciechowska, et al.
Organic & Biomolecular Chemistry|August 31, 2022
Symmetry-driven diastereoselective functionalization of simple trianglaminePaweł Skowronek, Natalia Prusinowska, Mateusz Bardziński, et al.
Chemistry, an Asian Journal|June 29, 2018
Sterically Crowded Trianglimines-Synthesis, Structure, Solid-State Self-Assembly, and Unexpected Chiroptical PropertiesNatalia Prusinowska, Mateusz Bardziński, Agnieszka Janiak, et al.
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