Zbigniew Wróbel

Kierownik zespołu
dr hab. Zbigniew Wróbel, prof. IChO PAN

Asystenci
Dr Andrzej Kwast

M. Walewska-Królikiewicz, B. Wilk, A. Kwast, Z. Wróbel, „Synthesis of various 1-alkylbenzimidazole derivatives directly from 2-alkylaminonitroarenes via a two-step, one-pot procedure”, J. Heterocyclic Chem.

M. Walewska-Królikiewicz, B. Wilk, A. Kwast, Z. Wróbel, „Comprehensive approach to the multigram, heavy-metal-free synthesis of 4-EWG-substituted quinoline derivatives”, Tetrahedron

M. Walewska-Królikiewicz, B. Wilk, A. Kwast, Z. Wróbel, „(2-Aminoaryl)iminophosphoranes as Versatile Starting Materials for the Synthesis of 1-Aryl-2-trifluoromethylbenzimidazoles”, Synlett

I. Kulszewicz-Bajer, R. Nowakowski, M. Zagórska, A. Maranda-Niedbała, W. Mech, Z. Wróbel, J. Drapała, I. Wielgus, K. P. Korona, „Copolymers Containing 1-Methyl-2-phenyl-imidazole Moieties as Permanent Dipole Generating Units: Synthesis, Spectroscopic, Electrochemical, and Photovoltaic Properties”, Molecules

Z. Wróbel, B. Wilk, P. Cmoch, A. Kwast, „The reported formation of 5 H ‐dibenzo [ b,e ][1,4]diazepin‐11( 10 H )‐ones in the noncatalyzed , base‐promoted double arylation of anthranilamide revisited. Correction of some product structures”, J. Heterocycl. Chem.

Z. Wróbel, B. Wilk, A. Kwast, „Substitution of a nitro group by diazonium salts in σH-Adducts of carbanions to mono-nitrobenzenes. Formation of substituted azobenzenes and indazoles”, Tetrahedron

M. Walewska-Królikiewicz, B. Wilk, A. Kwast, Z. Wróbel, „Two-step, regioselective, multigram-scale synthesis of 2-(trifluoromethyl)indoles from 2-nitrotoluenes”, Tetrahedron Lett.

G. Spólnik, P. Wach, Z. Wróbel, W. Danikiewicz, „2-Iodomalondialdehyde is an abundant component of soluble organic iodine in atmospheric wet precipitation”, Science of The Total Environment

P. Kowalik, P. Bujak, Z. Wróbel, M. Penkala, K. Kotwica, A. Maroń, A. Proń, „From Red to Green Luminescence via Surface Functionalization. Effect of 2-(5-Mercaptothien-2-yl)-8-(thien-2-yl)-5-hexylthieno[3,4-c]pyrrole-4,6-dione Ligands on the Photoluminescence of Alloyed Ag–In–Zn–S Nanocrystals”, Inorg. Chem.

M. Tryniszewski, R. Bujok, R. Gańczarczyk, Z. Wróbel, „Reductive Condensation of a Nitro Group with Carboxylic Acids Promoted by Phosphorus(III) Compounds: A Short Route to 5H-Dibenzo[b,e][1,4]diazepin-11(10H)-ones”, Synthesis

T. Marszałek, I. Krygier, A. Proń, Z. Wróbel, P.M.W. Blom, I. Kulszewicz-Bajer, W. Pisula, „Self-assembly and charge carrier transport of sublimated dialkyl substituted quinacridones”, Org. Electron.

M. Tryniszewski, R. Bujok, P. Cmoch, R. Gańczarczyk, I. Kulszewicz-Bajer, Z. Wróbel, „Direct Reductive Cyclocondensation of the Nitro Group with the Amido Group: Key Role of the Iminophosphorane Intermediate in the Synthesis of 1,4-Dibenzodiazepine Derivatives”, J. Org. Chem.

P. Bujak, Z. Wróbel, M. Penkala, K. Kotwica, A. Kmita, M. Gajewska, A. Ostrowski, P. Kowalik, A. Proń, „Highly Luminescent Ag–In–Zn–S Quaternary Nanocrystals: Growth Mechanism and Surface Chemistry Elucidation”, Inorg. Chem.

Z. Wróbel, R. Bujok, M. Tryniszewski, A. Kwast, “Simple synthesis of 2-alkylidene- and 2-keto-7-triazolylquinoxaline systems from 2-nitrosodiarylamines”, Arkivoc

R. Bujok, M. Wiszniewski, P. Cmoch, Z. Wróbel, “A general and convenient method for the synthesis of 2,4-dinitrobenzyl ketones. Almost unlimited access to 2-substituted 6-nitroindoles from 2,4-dinitrotoluene and aldehydes”, New J. Chem.

R. Bujok, P. Cmoch, Z. Wróbel, K. Wojciechowski, „Transition-metal-free synthesis of 3-(1-pyrrolidinyl)quinolines and 3-(1-pyrrolidinyl)quinoline 1-oxides via a one-pot reaction of 3-(1-pyrrolidinyl)crotonates with nitrobenzenes”, Org. Biomol. Chem.

Z.Wróbel, K. Plichta, A. Kwast, “Reactivity and substituent effects in the cyclization of N-aryl-2-nitrosoanilines to phenazines”, Tetrahedron

Ł. Skórka, P. Kurzep, G. Wiosna-Sałyga, B. Łuczyńska, I. Wielgus, Z. Wróbel, J. Ulański, I. Kulszewicz-Bajer, „New diarylaminophenyl derivatives of carbazole: Effect of substituent position on their redox, spectroscopic and electroluminescent properties”, Synth. Met.