Karol Grela

Kierownik zespołu
Prof. dr hab. Karol Grela

R. Kusy, K. Grela, „Protocol for (E)-selective semihydrogenation of alkynes using iridium-based catalyst”, STAR Protocols

A. Kajetanowicz, K. Grela, „Nitro and Other Electron Withdrawing Group Activated Ruthenium Catalysts for Olefin Metathesis Reactions”, Angew. Chem. Int. Ed.

K. Grela, R. Kusy, „Ligand-Free (Z)-Selective Transfer Semihydrogenation of Alkynes Catalyzed by in situ Generated Oxidizable Copper Nanoparticles”, Green Chem.

R. Gajda, A. Poater, A. Brotons-Rufes, S. Planer, K Woźniak, K. Grela, A. Kajetanowicz, „Aminomethylpyridinequinones as new ligands for PEPPSI-type complexes”, Arkivoc

K. Grela, A.  Kajetanowicz, A. Szadkowska, J. Czaban-Jóźwiak, „Alkene Cross-Metathesis Reactions”, Org. React.

A. Kajetanowicz, K. Grela, „Nitro and Other Electron Withdrawing Group Activated Ruthenium Catalysts for Olefin Metathesis Reactions”, Angew. Chem. Int. Ed.

Ł. Woźniak, A. A. Rajkiewicz, L. Monsigny, A. Kajetanowicz, K Grela, „Preparation of Functionalized α,β-Unsaturated Sulfonamides via Olefin Cross-Metathesis”, Org. Lett.

M. Pieczykolan, J.Czaban-Jóźwiak, M. Malinska, K. Woźniak, R. Dorta, A. Rybicka, A. Kajetanowicz, K. Grela, „The Influence of Various N-Heterocyclic Carbene Ligands on Activity of Nitro-Activated Olefin Metathesis Catalysts”, Molecules

M. Bieniek, R. Bujok, M. Milewski, D. Arlt, A. Kajetanowicz, K. Grela, „Making the family portrait complete: Synthesis of Electron Withdrawing Group activated Hoveyda-Grubbs catalysts bearing sulfone and ketone functionalities”, J. Organomet. Chem.

A. Sytniczuk, G. Forcher, D.B. Grotjahn, K. Grela, „Sequential Alkene Isomerization and Ring-Closing Metathesis in Production of Macrocyclic Musks from Biomass”, Chem. Eur. J.

G.K. Zieliński, J. Majtczak, M. Gutowski, K. Grela, „A Selective and Functional Group-Tolerant Ruthenium-Catalyzed Olefin Metathesis/Transfer Hydrogenation Tandem Sequence Using Formic Acid as Hydrogen Source”, J. Org. Chem.

K. Młodzikowska, A.A. Rajkiewicz, K. Grela, B. Trzaskowski, „Boron–boron, carbon–carbon and nitrogen–nitrogen bonding in N-heterocyclic carbenes and their diazaboryl and triazole analogues: Wanzlick equilibrium revisited”, New J. Chem.

A. Zieliński, G. Szczepaniak, R. Gajda, K. Woźniak, B. Trzaskowski, D. Vidović, A. Kajetanowicz, K. Grela, „Ruthenium Olefin Metathesis Catalysts Systematically Modified in Chelating Benzylidene Ether Fragment: Experiment and Computations”, Eur. J. Inorg. Chem.

J. Czaban-Jóźwiak, Ł. Woźniak, A. Ulikowski, K. Kwiecińska, A.A. Rajkiewicz, K. Grela, „Modification of Polyhedral Oligomeric Silsesquioxanes (POSS) Molecules by Ruthenium Catalyzed Cross Metathesis”, Molecules

A. Sytniczuk, A. Kajetanowicz, K. Grela, „Fishing for the right catalyst for the cross-metathesis reaction of methyl oleate with 2-methyl-2-butene”, Catal. Sci. Technol.

A. Kajetanowicz, M. Milewski, J. Rogińska, R. Gajda, K. Woźniak, „Hoveyda-Type Quinone-Containing Complexes – Catalysts to Prevent Migration of the Double Bond under Metathesis Conditions”, Eur. J. Org. Chem.

G. Zieliński, K. Grela, „Tandem Catalysis Utilizing Olefin Metathesis Reactions”, Chem. Eur. J.

K. Skowerski, J. Białecki, S. J. Czarnocki, K. Żukowska, K. Grela, „Effective immobilisation of a metathesis catalyst bearing an ammonium-tagged NHC ligand on various solid supports”, Beilstein J. Org. Chem.

G. K. Zieliński, C. Samojłowicz, T. Wdowik, K. Grela, „In tandem or alone: a remarkably selective transfer hydrogenation of alkenes catalyzed by ruthenium olefin metathesis catalysts”, Org. Biomol. Chem.

K. Grela, „Progress in metathesis chemistry II”, Beilstein J. Org. Chem.

G. Szczepaniak, K. Urbaniak, C. Wierzbicka, K. Kosiński, K. Skowerski, K. Grela, „High-Performance Isocyanide Scavengers for Use in Low-Waste Purification of Olefin Metathesis Products”, ChemSusChem