Dr Jacek Wojaczyński

Contact information

Address:

Department of Chemistry, University of Wrocław,
14 F. Joliot-Curie St.
50-383 Wrocław, POLAND

Phone:

(48) (71) 3757276 (room 1067, office)
(48) (71) 3757628 (room 1071, lab)

E-mail:

jacek.wojaczynski[at]chem.uni.wroc.pl

Research Interests

Supramolecular chemistry. NMR spectroscopy including paramagnetic compounds. Stereochemistry. History of chemistry. Degradation of porphyrinoids.

Selected Papers

Szterenberg, L.; Latos-Grażyński, L.; Wojaczyński, J. Metallobiliverdin Radicals - DFT Studies. ChemPhysChem 2003, 4, 691.

Wójtowicz, H.; Wojaczyński, J.; Olczak, M.; Króliczewski, J.; Latos-Grażyński, L.; Olczak, T. Heme environment in HmuY, the heme-binding protein of Porphyromonas gingivalis. Biochem. Biophys. Res. Commun.2009383, 178.

Wojaczyński, J.; Latos-Grażyński, L. Photooxidation of N-Confused Porphyrin: A Route to N-Confused Biliverdin Analogues. Chem. Eur. J. 201016, 2679.

Wojaczyńska, E.; Wojaczyński, J. Enantioselective Synthesis of Sulfoxides: 2000 - 2009. Chem. Rev. 2010110, 4303.

Wójtowicz, H.; Bielecki, M.; Wojaczyński, J.; Olczak, M.; Smalley, J. W.; Olczak, T. The Porphyromonas gingivalis HmuY haemophore binds gallium(III), zinc(II), cobalt(III), manganese(III), nickel(II), and copper(II) protoporphyrin IX but in a manner different to iron(III) protoporphyrin IX. Metallomics 20135, 343.

Wojaczyński, J. Degradation Pathways for Porphyrinoids. Topics in Heterocyclic Chemistry 2014, 33, 143.

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.

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. 201513, 6116.

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 reactionsNew J. Chem. 2016, 40, 9795. 

Wojaczyńska, E.; Kamińska, K.; Wojaczyński, J.; Skarżewski, J., Chiral pyrrolidine thioethers and 2-azanorbornane derivatives bearing additional nitrogen functions. Enantiopure ligands for palladium-catalyzed Tsuji-Trost reaction. Arkivoc 2017, ii, 162.

(See the complete publication list of our group.)