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Faculty of Computer Science and Management

Prof. Elżbieta Wojaczyńska, DSc, PhD, Eng

Email: elzbieta.wojaczynska@pwr.edu.pl

Unit: Faculty of Chemistry » Department of Physical and Quantum Chemistry

Elżbieta WojaczyńskaWybrzeże Wyspiańskiego 29, 50-371 Wrocław
building A-2, room 219, 220
phone +48 71 320 2410

Dean's plenipotentiary for the faculty promotion

Rector’s plenipotentiary for the Lower Silesian Science Festival

Research fields

  • Stereoselective synthesis as a tool for preparation of chiral compounds useful as building blocks, ligands or organocatalysts and exhibiting biological activity, in particular: asymmetric aza-Diels-Alder reaction, stereoselective Mannich reaction, preparation of chiral polyampholites.

Recent papers

2023

  • Wojaczyńska E., Wojaczyński J., Chiral sulfinyls from sulfones, Nat. Chem. 2023, 15,
    165-166.

2022

  • Iwan D., Kamińska K., Denel-Bobrowska M., Olejniczak A.B., Wojaczyńska E. Chiral
    sulfonamides wth various N-heterocyclic and aromatic units – synthesis and antiviral
    activity evaluation, Biomed. Pharmacother. 2022, 153, 113473.
  • Kamińska K., Iwan D., Iglesias-Reguant A., Spałek W., Daszkiewicz M., Sobolewska A.,
    Zaleśny R., Wojaczyńska E., Bartkiewicz S., Synthesis, spectroscopic and computational
    studies of photochromic azobenzene derivatives with 2-azabicycloalkane scaffold, J. Mol.
    Liq. 2022, 363, 119869.

2021

  • Steppeler F., Kłopotowska D., Wietrzyk J., Wojaczyńska E., Synthesis and
    antiproliferative activity of triazoles based on 2-azabicycloalkanes, Materials 2021, 14,
    2039.

2020

  • Wojaczyńska E., Wojaczyński J., Modern stereoselective synthesis of chiral sulfinyl
    compounds, Chem. Rev. 2020, 120, 4578-4611.
  • Iwanejko J., Sowiński M., Wojaczyńska E., Olszewski T.K., Górecki M., An approach to
    new chiral bicyclic imines nd amines via Horner-Wadsworth-Emmons reaction, RCS Adv.
    2020, 10, 14618-14629.

2019

  • Miniewicz A., Bartkiewicz S., Wojaczyńska E., Galica T., Zaleśny R., Jakubas R., Second
    harmonic generation in nonlinear optical crystal formed of propellane-type molecule, J.
    Mater. Chem. C 2019, 7, 1255-1262.
  • Iwanejko J., Brol A., Szyja B., Daszkiewicz M., Wojaczyńska E., Olszewski T.K.,
    Aminophosphonates and aminophosphonic acids with tetrasubstituted stereogenic center:
    diastereoselective synthesis from cyclic ketimines, Org. Biomol. Chem. 2019, 17, 7352-
    7359.

2018 

  • Iwanejko J., Wojaczyńska E., Cyclic imines – preparation and application in synthesis,
    Org. Biomol. Chem. 2018, 16, 7296-7314.


2017

  • Kamińska K., Wojaczyńska E., Skarżewski J., Kochel A., Wojaczyński J., Application of
    sulfonyl chlorides and chiral amines in the efficient synthesis of nonracemic sulfinamides,
    Tetrahedron: Asymmetry 2017, 28, 561-566.
  • Kamińska K., Wojaczyńska E., Santi C., Sancineto L., Pensa M. F., Kochel A., Wieczorek
    R., Wojaczyński J., Slupski G., Tetrahedron: Asymmetry 2017, 28, 1367-1372.

2016

  • Wojaczyńska E., Skarżewski J., Sidorowicz Ł., Wieczorek R., Wojaczyński J., Zinc complexes formed by 2,2'-bipyridine and 1,10-phenanthroline moieties combined with 2-azanorbornane: modular chiral catalysts for aldol reactions, New J. Chem. 2016, 40, 9795-9805.

2015

  • Wojaczyńska E., Wojaczyński J., Kleniewska K., Dorsz M., Olszewski T.K., 2-Azanorbornane - a versatile chiral aza-Diels-Alder cycloadduct: preparation, applications in stereoselective synthesis and biological activity, Org. Biomol. Chem. 2015, 13, 6116-6148.

2014

  • Iwanejko J., Wojaczyńska E., Wojaczyński J., Bąkowicz J., Stereoselective preparation of chiral compounds in Mannich-type reactions of a bicyclic imine and phenols or indole, Tetrahedron Lett. 2014, 55, 6619-6622.

2013

  • Wojaczyńska E., Bąkowicz J., Dorsz M., Skarżewski J., Monoimine derived from trans-1,2-diaminocyclohexane and ethyl glyoxylate: an intermediate in aza-Diels-Alder and Mannich reactions, J. Org. Chem. 2013, 78, 2808-2811.

2010

  • Wojaczyńska E., Wojaczyński J., Enantioselective synthesis of sulfoxides 2000-2009, Chem. Rev. 2010, 110, 4303-4356.
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