Year |
Citation |
Score |
2023 |
Sytniczuk A, Struzik F, Grela K, Kajetanowicz A. A tunable family of CAAC-ruthenium olefin metathesis catalysts modularly derived from a large-scale produced ibuprofen intermediate. Chemical Science. 14: 10744-10755. PMID 37829018 DOI: 10.1039/d3sc03849a |
0.507 |
|
2022 |
Grzesiński Ł, Milewski M, Nadirova M, Kajetanowicz A, Grela K. Unexpected Latency of -Stereoretentive Ruthenium Olefin Metathesis Catalysts Bearing Unsymmetrical N-heterocyclic Carbene or Cyclic(alkyl)(amino)carbene Ligands. Organometallics. 42: 2453-2459. PMID 37772273 DOI: 10.1021/acs.organomet.2c00428 |
0.524 |
|
2022 |
Tyszka-Gumkowska A, Kajetanowicz A, Grela K. Protocol for olefin metathesis reactions of hydrophobic substrates performed in aqueous emulsion with mechanical stirring or with microwaves support. Star Protocols. 3: 101671. PMID 36149799 DOI: 10.1016/j.xpro.2022.101671 |
0.408 |
|
2022 |
Tyszka-Gumkowska A, Purohit VB, Nienałtowski T, Dąbrowski M, Kajetanowicz A, Grela K. Testing enabling techniques for olefin metathesis reactions of lipophilic substrates in water as a diluent. Iscience. 25: 104131. PMID 35434568 DOI: 10.1016/j.isci.2022.104131 |
0.679 |
|
2022 |
Kośnik W, Lichosyt D, Śnieżek M, Janaszkiewicz A, Woźniak K, Malińska M, Trzaskowski B, Kajetanowicz A, Grela K. Ruthenium Olefin Metathesis Catalysts Bearing a Macrocyclic N-Heterocyclic Carbene Ligand: Improved Stability and Activity. Angewandte Chemie (International Ed. in English). e202201472. PMID 35347824 DOI: 10.1002/anie.202201472 |
0.513 |
|
2021 |
Monsigny L, Cejas Sánchez J, Piątkowski J, Kajetanowicz A, Grela K. Synthesis and Catalytic Properties of a Very Latent Selenium-Chelated Ruthenium Benzylidene Olefin Metathesis Catalyst. Organometallics. 40: 3608-3616. PMID 34776582 DOI: 10.1021/acs.organomet.1c00484 |
0.49 |
|
2021 |
Czarnocki S, Monsigny L, Sienkiewicz M, Kajetanowicz A, Grela K. Ruthenium Olefin Metathesis Catalysts Featuring N-Heterocyclic Carbene Ligands Tagged with Isonicotinic and 4-(Dimethylamino)benzoic Acid Rests: Evaluation of a Modular Synthetic Strategy. Molecules (Basel, Switzerland). 26. PMID 34500654 DOI: 10.3390/molecules26175220 |
0.47 |
|
2021 |
Monsigny L, Kajetanowicz A, Grela K. Ruthenium Complexes Featuring Unsymmetrical N-Heterocyclic Carbene Ligands-Useful Olefin Metathesis Catalysts for Special Tasks. Chemical Record (New York, N.Y.). 21: 3648-3661. PMID 34145741 DOI: 10.1002/tcr.202100126 |
0.478 |
|
2020 |
Nienałtowski T, Krzesiński P, Baumert ME, Skoczeń A, Suska-Kauf E, Pawłowska J, Kajetanowicz A, Grela K. 4-Methyltetrahydropyran as a Convenient Alternative Solvent for Olefin Metathesis Reaction: Model Studies and Medicinal Chemistry Applications. Acs Sustainable Chemistry & Engineering. 8: 18215-18223. PMID 33344098 DOI: 10.1021/acssuschemeng.0c06668 |
0.345 |
|
2020 |
Nienałtowski T, Szczepanik P, Małecki P, Czajkowska-Szczykowska D, Czarnocki S, Pawłowska J, Kajetanowicz A, Grela K. Large-Scale Synthesis of a Niche Olefin Metathesis Catalyst Bearing an Unsymmetrical N-Heterocyclic Carbene (NHC) Ligand and its Application in a Green Pharmaceutical Context. Chemistry (Weinheim An Der Bergstrasse, Germany). 26: 15708-15717. PMID 33210346 DOI: 10.1002/chem.202003830 |
0.503 |
|
2020 |
Planer S, Małecki P, Trzaskowski B, Kajetanowicz A, Grela K. Sterically Tuned N-Heterocyclic Carbene Ligands for the Efficient Formation of Hindered Products in Ru-Catalyzed Olefin Metathesis Acs Catalysis. PMID 33123411 DOI: 10.1021/Acscatal.0C02770 |
0.414 |
|
2020 |
Grela K, Kajetanowicz A. Nitro and Other Electron Withdrawing Group-Activated Ruthenium Catalysts for Olefin Metathesis Reaction. Angewandte Chemie. PMID 32808704 DOI: 10.1002/Anie.202008150 |
0.61 |
|
2020 |
Woźniak Ł, Rajkiewicz AA, Monsigny L, Kajetanowicz A, Grela K. Preparation of Functionalized α,β-Unsaturated Sulfonamides via Olefin Cross-Metathesis Organic Letters. 22: 4970-4973. PMID 32610933 DOI: 10.1021/Acs.Orglett.0C01471 |
0.342 |
|
2020 |
Pieczykolan M, Czaban-Jóźwiak J, Malinska M, Woźniak K, Dorta R, Rybicka A, Kajetanowicz A, Grela K. The Influence of Various -Heterocyclic Carbene Ligands on Activity of Nitro-Activated Olefin Metathesis Catalysts. Molecules (Basel, Switzerland). 25. PMID 32408688 DOI: 10.3390/Molecules25102282 |
0.591 |
|
2020 |
Dąbrowski M, Wyrębek P, Trzybiński D, Woźniak K, Grela K. In a Quest for Selectivity Paired with Activity: A Ruthenium Olefin Metathesis Catalyst Bearing an Unsymmetrical Phenanthrene-Based N-Heterocyclic Carbene. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32133701 DOI: 10.1002/Chem.201904549 |
0.76 |
|
2020 |
Jolly PI, Marczyk A, Małecki P, Trzybiński D, Woźniak K, Kajetanowicz A, Grela K. Specialized Olefin Metathesis Catalysts Featuring Unsymmetrical N-Heterocyclic Carbene Ligands Bearing N-(Fluoren-9-yl) Arm Catalysts. 10: 599. DOI: 10.3390/Catal10060599 |
0.48 |
|
2020 |
Chołuj A, Nogaś W, Patrzałek M, Krzesiński P, Chmielewski MJ, Kajetanowicz A, Grela K. Preparation of Ruthenium Olefin Metathesis Catalysts Immobilized on MOF, SBA-15, and 13X for Probing Heterogeneous Boomerang Effect Catalysts. 10: 438. DOI: 10.3390/Catal10040438 |
0.591 |
|
2020 |
Sytniczuk A, Milewski M, Kajetanowicz A, Grela K. Preparation of macrocyclic musks via olefin metathesis: comparison with classical syntheses and recent advances Russian Chemical Reviews. 89: 469-490. DOI: 10.1070/Rcr4930 |
0.419 |
|
2020 |
Szczepaniak G, Piątkowski J, Nogaś W, Lorandi F, Yerneni SS, Fantin M, Ruszczyńska A, Enciso AE, Bulska E, Grela K, Matyjaszewski K. An isocyanide ligand for the rapid quenching and efficient removal of copper residues after Cu/TEMPO-catalyzed aerobic alcohol oxidation and atom transfer radical polymerization Chemical Science. 11: 4251-4262. DOI: 10.1039/D0Sc00623H |
0.7 |
|
2020 |
Bieniek M, Bujok R, Milewski M, Arlt D, Kajetanowicz A, Grela K. Making the family portrait complete: Synthesis of Electron Withdrawing Group activated Hoveyda-Grubbs catalysts bearing sulfone and ketone functionalities Journal of Organometallic Chemistry. 918: 121276. DOI: 10.1016/J.Jorganchem.2020.121276 |
0.846 |
|
2019 |
Planer S, Jana A, Grela K. Ethyl Lactate: A Green Solvent for Olefin Metathesis. Chemsuschem. 12: 4655-4661. PMID 31412165 DOI: 10.1002/Cssc.201901735 |
0.577 |
|
2019 |
Patrzałek M, Piątkowski J, Kajetanowicz A, Grela K. Anion Metathesis in Facile Preparation of Olefin Metathesis Catalysts Bearing a Quaternary Ammonium Chloride Tag Synlett. 30: 1981-1987. DOI: 10.1055/S-0037-1611834 |
0.624 |
|
2019 |
Chołuj A, Krzesiński P, Ruszczyńska A, Bulska E, Kajetanowicz A, Grela K. Noncovalent Immobilization of Cationic Ruthenium Complex in a Metal–Organic Framework by Ion Exchange Leading to a Heterogeneous Olefin Metathesis Catalyst for Use in Green Solvents Organometallics. 38: 3397-3405. DOI: 10.1021/Acs.Organomet.9B00287 |
0.572 |
|
2019 |
Szczepaniak G, Nogaś W, Piątkowski J, Ruszczyńska A, Bulska E, Grela K. Semiheterogeneous Purification Protocol for the Removal of Ruthenium Impurities from Olefin Metathesis Reaction Products Using an Isocyanide Scavenger Organic Process Research & Development. 23: 836-844. DOI: 10.1021/Acs.Oprd.8B00392 |
0.73 |
|
2019 |
Smoleń M, Marczyk A, Kośnik W, Trzaskowski B, Kajetanowicz A, Grela K. Ruthenium-Catalysed Olefin Metathesis in Environmentally Friendly Solvents: 2-Methyltetrahydrofuran Revisited European Journal of Organic Chemistry. 2019: 640-646. DOI: 10.1002/Ejoc.201801741 |
0.373 |
|
2019 |
Kajetanowicz A, Chwalba M, Gawin A, Tracz A, Grela K. Non‐Glovebox Ethenolysis of Ethyl Oleate and FAME at Larger Scale Utilizing a Cyclic (Alkyl)(Amino)Carbene Ruthenium Catalyst European Journal of Lipid Science and Technology. 122: 1900263. DOI: 10.1002/Ejlt.201900263 |
0.549 |
|
2019 |
Jana A, Zieliński GK, Czarnocka‐Śniadała S, Grudzień K, Podwysocka D, Szulc M, Kajetanowicz A, Grela K. Synthesis of Substituted β‐Functionalised Styrenes by Microwave‐Assisted Olefin Cross‐Metathesis and Scalable Synthesis of Apremilast Chemcatchem. 11: 5808-5813. DOI: 10.1002/Cctc.201901473 |
0.386 |
|
2019 |
Mukherjee N, Marczyk A, Szczepaniak G, Sytniczuk A, Kajetanowicz A, Grela K. A Gentler Touch: Synthesis of Modern Ruthenium Olefin Metathesis Catalysts Sustained by Mechanical Force Chemcatchem. 11: 5362-5369. DOI: 10.1002/Cctc.201901444 |
0.781 |
|
2018 |
Wyrębek P, Małecki P, Sytniczuk A, Kośnik W, Gawin A, Kostrzewa J, Kajetanowicz A, Grela K. Looking for the Noncyclic(amino)(alkyl)carbene Ruthenium Catalyst for Ethenolysis of Ethyl Oleate: Selectivity Is on Target. Acs Omega. 3: 18481-18488. PMID 31458420 DOI: 10.1021/acsomega.8b03119 |
0.496 |
|
2018 |
Smoleń M, Kośnik W, Gajda R, Woźniak K, Skoczeń A, Kajetanowicz A, Grela K. Ruthenium Complexes Bearing Thiophene-Based Unsymmetrical N-Heterocyclic Carbene Ligands as Selective Catalysts for Olefin Metathesis in Toluene and Environmentally Friendly 2-Methyltetrahydrofuran. Chemistry (Weinheim An Der Bergstrasse, Germany). 24: 15372-15379. PMID 30230657 DOI: 10.1002/Chem.201803460 |
0.568 |
|
2018 |
Sytniczuk A, Leszczyńska A, Kajetanowicz A, Grela K. Preparation of Musk-Smelling Macrocyclic Lactones from Biomass: Looking for the Optimal Substrate Combination. Chemsuschem. 11: 3157-3166. PMID 30028581 DOI: 10.1002/Cssc.201801463 |
0.34 |
|
2018 |
Czaban-Jóźwiak J, Woźniak Ł, Ulikowski A, Kwiecińska K, Rajkiewicz AA, Grela K. Modification of Polyhedral Oligomeric Silsesquioxanes (POSS) Molecules by Ruthenium Catalyzed Cross Metathesis. Molecules (Basel, Switzerland). 23. PMID 30011916 DOI: 10.3390/Molecules23071722 |
0.52 |
|
2018 |
Sytniczuk A, Dąbrowski M, Banach U, Urban M, Czarnocka-Śniadała S, Milewski M, Kajetanowicz A, Grela K. At Long Last: Olefin Metathesis Macrocyclization at High Concentration. Journal of the American Chemical Society. PMID 29944361 DOI: 10.1021/Jacs.8B04820 |
0.72 |
|
2018 |
Sytniczuk A, Forcher G, Grotjahn DB, Grela K. Sequential Alkene Isomerization and Ring-Closing Metathesis in Production of Macrocyclic Musks from Biomass. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29931831 DOI: 10.1002/Chem.201800728 |
0.401 |
|
2018 |
Karras M, Dąbrowski M, Pohl R, Rybáček J, Vacek J, Bednárová L, Grela K, Starý I, Stará IG, Schmidt B. Helicenes as chirality inducing groups in transition metal catalysis: the first helically chiral olefin metathesis catalyst. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29917281 DOI: 10.1002/Chem.201802786 |
0.753 |
|
2018 |
Michalska M, Grudzień K, Małecki P, Grela K. Gold(I)-Catalyzed Formation of Naphthalene/Acenaphthene Heterocyclic Acetals. Organic Letters. 20: 954-957. PMID 29412677 DOI: 10.1021/Acs.Orglett.7B03856 |
0.401 |
|
2018 |
Jolly PI, Marczyk A, Małecki P, Ablialimov O, Trzybiński D, Woźniak K, Osella S, Trzaskowski B, Grela K. Azoliniums, Adducts, NHCs and Azomethine Ylides: Divergence in Wanzlick Equilibrium and Olefin Metathesis Catalyst Formation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29405499 DOI: 10.1002/Chem.201706036 |
0.514 |
|
2018 |
Zieliński GK, Majtczak J, Gutowski M, Grela K. A Selective and Functional Group Tolerant Ruthenium Catalyzed Olefin Metathesis/Transfer Hydrogenation Tandem Sequence Using Formic Acid as Hydrogen Source. The Journal of Organic Chemistry. PMID 29302962 DOI: 10.1021/Acs.Joc.7B02468 |
0.393 |
|
2018 |
Jana A, Grela K. Forged and fashioned for faithfulness-ruthenium olefin metathesis catalysts bearing ammonium tags. Chemical Communications (Cambridge, England). 54: 122-139. PMID 29188265 DOI: 10.1039/C7Cc06535C |
0.599 |
|
2018 |
Grudzień K, Trzaskowski B, Smoleń M, Gajda R, Woźniak K, Grela K. Hoveyda-Grubbs catalyst analogues bearing the derivatives of N-phenylpyrrol in the carbene ligand - structure, stability, activity and unique ruthenium-phenyl interactions. Dalton Transactions (Cambridge, England : 2003). 46: 11790-11799. PMID 28829469 DOI: 10.1039/C7Dt02180A |
0.492 |
|
2018 |
Młodzikowska K, Rajkiewicz AA, Grela K, Trzaskowski B. Boron–boron, carbon–carbon and nitrogen–nitrogen bonding in N-heterocyclic carbenes and their diazaboryl and triazole analogues: Wanzlick equilibrium revisited New Journal of Chemistry. 42: 6183-6190. DOI: 10.1039/C8Nj00296G |
0.306 |
|
2018 |
Mukherjee N, Planer S, Grela K. Formation of tetrasubstituted C–C double bonds via olefin metathesis: challenges, catalysts, and applications in natural product synthesis Organic Chemistry Frontiers. 5: 494-516. DOI: 10.1039/C7Qo00800G |
0.465 |
|
2018 |
Szczepaniak G, Ruszczyńska A, Kosiński K, Bulska E, Grela K. Highly efficient and time economical purification of olefin metathesis products from metal residues using an isocyanide scavenger Green Chemistry. 20: 1280-1289. DOI: 10.1039/C7Gc03324A |
0.689 |
|
2018 |
Małecki P, Gajda K, Gajda R, Woźniak K, Trzaskowski B, Kajetanowicz A, Grela K. Specialized Ruthenium Olefin Metathesis Catalysts Bearing Bulky Unsymmetrical NHC Ligands: Computations, Synthesis, and Application Acs Catalysis. 9: 587-598. DOI: 10.1021/Acscatal.8B04783 |
0.619 |
|
2018 |
Mukherjee N, Gawin R, Czarnocki SJ, Gajda R, Malińska M, Woźniak K, Kajetanowicz A, Grela K. Unexpected formation of nitroso-chelated cyclic η1-acylruthenium(II) complex, an effective catalysts for transfer hydrogenation reaction Journal of Organometallic Chemistry. 867: 359-366. DOI: 10.1016/J.Jorganchem.2018.01.035 |
0.55 |
|
2018 |
Gawin A, Małecki P, Dranka M, Zachara J, Skompska M, Kajetanowicz A, Grela K. An unexpected formation of a Ru(III) benzylidene complex during activation of a LatMet-type ring-opening polymerisation catalyst Journal of Catalysis. 364: 345-353. DOI: 10.1016/J.Jcat.2018.05.014 |
0.498 |
|
2018 |
Zieliński A, Szczepaniak G, Gajda R, Woźniak K, Trzaskowski B, Vidović D, Kajetanowicz A, Grela K. Ruthenium Olefin Metathesis Catalysts Systematically Modified in Chelating Benzylidene Ether Fragment: Experiment and Computations European Journal of Inorganic Chemistry. 2018: 3675-3685. DOI: 10.1002/Ejic.201800639 |
0.833 |
|
2018 |
Gawin A, Pump E, Slugovc C, Kajetanowicz A, Grela K. Ruthenium Amide Complexes - Synthesis and Catalytic Activity in Olefin Metathesis and in Ring-Opening Polymerisation European Journal of Inorganic Chemistry. 2018: 1766-1774. DOI: 10.1002/Ejic.201800251 |
0.484 |
|
2017 |
Jana A, Trzybiński D, Woźniak K, Grela K. Well-Defined Chiral Copper NHC Complex in the Asymmetric Conjugated β-Borylation and One-Pot Metathesis-Asymmetric β-Borylation Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 24: 891-897. PMID 29120504 DOI: 10.1002/Chem.201704335 |
0.517 |
|
2017 |
Jana A, Misztal K, Żak A, Grela K. Synthesis of Selectively Substituted or Deuterated Indenes via Sequential Pd and Ru Catalysis. The Journal of Organic Chemistry. 82: 4226-4234. PMID 28332398 DOI: 10.1021/Acs.Joc.7B00200 |
0.399 |
|
2017 |
Jana A, Grela K. Correction to "Mild Functionalization of Tetraoxane Derivatives via Olefin Metathesis: Compatibility of Ruthenium Alkylidene Catalysts with Peroxides". Organic Letters. 19: 1256. PMID 28225283 DOI: 10.1021/acs.orglett.7b00413 |
0.491 |
|
2017 |
Jana A, Grela K. Mild Functionalization of Tetraoxane Derivatives via Olefin Metathesis: Compatibility of Ruthenium Alkylidene Catalysts with Peroxides. Organic Letters. 19: 520-523. PMID 28094973 DOI: 10.1021/Acs.Orglett.6B03688 |
0.467 |
|
2017 |
Sytniczuk A, Kajetanowicz A, Grela K. Fishing for the right catalyst for the cross-metathesis reaction of methyl oleate with 2-methyl-2-butene Catalysis Science & Technology. 7: 1284-1296. DOI: 10.1039/C6Cy02623K |
0.439 |
|
2017 |
Czarnocki SJ, Czeluśniak I, Olszewski TK, Malinska M, Woźniak K, Grela K. Rational and Then Serendipitous Formation of Aza Analogues of Hoveyda-Type Catalysts Containing a Chelating Ester Group Leading to a Polymerization Catalyst Family Acs Catalysis. 7: 4115-4121. DOI: 10.1021/Acscatal.7B00843 |
0.622 |
|
2017 |
Paradiso V, Bertolasi V, Costabile C, Caruso T, Dąbrowski M, Grela K, Grisi F. Expanding the Family of Hoveyda–Grubbs Catalysts Containing Unsymmetrical NHC Ligands Organometallics. 36: 3692-3708. DOI: 10.1021/Acs.Organomet.7B00488 |
0.584 |
|
2017 |
Małecki P, Gajda K, Ablialimov O, Malińska M, Gajda R, Woźniak K, Kajetanowicz A, Grela K. Hoveyda–Grubbs-Type Precatalysts with UnsymmetricalN-Heterocyclic Carbenes as Effective Catalysts in Olefin Metathesis Organometallics. 36: 2153-2166. DOI: 10.1021/Acs.Organomet.7B00211 |
0.592 |
|
2017 |
Trzaskowski B, Goddard W, Grela K. Faster initiating olefin metathesis catalysts from introducing double bonds into cyclopropyl, cyclobutyl and cyclopentyl derivatives of Hoveyda-Grubbs precatalysts Molecular Catalysis. 433: 313-320. DOI: 10.1016/J.Mcat.2016.12.018 |
0.491 |
|
2017 |
Szwaczko K, Czeluśniak I, Grela K. A partially serendipitous discovery of thermo-switchable ruthenium olefin metathesis initiator that seem to be well suited for ROMP of monomers bearing vinyl pendant groups Journal of Organometallic Chemistry. 847: 146-153. DOI: 10.1016/J.Jorganchem.2017.04.003 |
0.525 |
|
2016 |
Kusy R, Grela K. E- and Z-Selective Transfer Semihydrogenation of Alkynes Catalyzed by Standard Ruthenium Olefin Metathesis Catalysts. Organic Letters. 18: 6196-6199. PMID 27934375 DOI: 10.1021/Acs.Orglett.6B03254 |
0.586 |
|
2016 |
César V, Zhang Y, Kośnik W, Zieliński A, Rajkiewicz AA, Ruamps M, Bastin S, Lugan N, Lavigne G, Grela K. Ruthenium Catalysts Supported by Amino-Substituted NHC Ligands for Olefin Metathesis of Challenging Substrates. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27914097 DOI: 10.1002/Chem.201604934 |
0.8 |
|
2016 |
Zieliński GK, Grela K. Tandem Catalysis Utilizing Olefin Metathesis Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 9440-54. PMID 27203528 DOI: 10.1002/Chem.201505136 |
0.518 |
|
2016 |
Skowerski K, Białecki J, Czarnocki SJ, Żukowska K, Grela K. Effective immobilisation of a metathesis catalyst bearing an ammonium-tagged NHC ligand on various solid supports. Beilstein Journal of Organic Chemistry. 12: 5-15. PMID 26877803 DOI: 10.3762/Bjoc.12.2 |
0.573 |
|
2016 |
Michalska M, Grela K. Simple and Mild Synthesis of Indoles via Hydroamination Reaction Catalysed by NHC-Gold Complexes: Looking for Optimized Conditions Synlett. 27: 599-603. DOI: 10.1055/S-0035-1560976 |
0.43 |
|
2016 |
Smoleń M, Kośnik W, Loska R, Gajda R, Malińska M, Woźniak K, Grela K. Synthesis and catalytic activity of ruthenium indenylidene complexes bearing unsymmetrical NHC containing a heteroaromatic moiety Rsc Advances. 6: 77013-77019. DOI: 10.1039/C6Ra18210K |
0.612 |
|
2016 |
Chołuj A, Zieliński A, Grela K, Chmielewski MJ. Metathesis@MOF: Simple and Robust Immobilization of Olefin Metathesis Catalysts inside (Al)MIL-101-NH2 Acs Catalysis. 6: 6343-6349. DOI: 10.1021/Acscatal.6B01048 |
0.82 |
|
2016 |
Trzaskowski B, Grela K. Hoveyda-Grubbs complexes with boryl anions are predicted to be fast metathesis catalysts Catalysis Communications. 86: 133-138. DOI: 10.1016/J.Catcom.2016.08.025 |
0.545 |
|
2016 |
Smolen M, Kosnik W, Loska R, Gajda R, Malinska M, Wozniak K, Grela K. ChemInform Abstract: Synthesis and Catalytic Activity of Ruthenium Indenylidene Complexes Bearing Unsymmetrical NHC Containing a Heteroaromatic Moiety. Cheminform. 47. DOI: 10.1002/chin.201647024 |
0.392 |
|
2016 |
Zieliński GK, Grela K. Cover Picture: Tandem Catalysis Utilizing Olefin Metathesis Reactions (Chem. Eur. J. 28/2016) Chemistry - a European Journal. 22: 9413-9413. DOI: 10.1002/Chem.201602589 |
0.383 |
|
2016 |
Żukowska K, Pączek Ł, Grela K. Sulfoxide-Chelated Ruthenium Benzylidene Catalyst: a Synthetic Study on the Utility of Olefin Metathesis Chemcatchem. 8: 2817-2823. DOI: 10.1002/Cctc.201600538 |
0.545 |
|
2015 |
Grela K. Progress in metathesis chemistry II. Beilstein Journal of Organic Chemistry. 11: 1639-40. PMID 26664583 DOI: 10.3762/Bjoc.11.179 |
0.579 |
|
2015 |
Szczepaniak G, Urbaniak K, Wierzbicka C, Kosiński K, Skowerski K, Grela K. High-Performance Isocyanide Scavengers for Use in Low-Waste Purification of Olefin Metathesis Products. Chemsuschem. 8: 4139-48. PMID 26556779 DOI: 10.1002/cssc.201500784 |
0.747 |
|
2015 |
Zieli?ski GK, Samoj?owicz C, Wdowik T, Grela K. In tandem or alone: a remarkably selective transfer hydrogenation of alkenes catalyzed by ruthenium olefin metathesis catalysts. Organic & Biomolecular Chemistry. 13: 2684-8. PMID 25586518 DOI: 10.1039/C4Ob02480J |
0.515 |
|
2015 |
Pazio A, Woźniak K, Grela K, Trzaskowski B. Nitrenium ions and trivalent boron ligands as analogues of N-heterocyclic carbenes in olefin metathesis: A computational study Dalton Transactions. 44: 20021-20026. DOI: 10.1039/C5Dt03446A |
0.397 |
|
2015 |
Pazio A, Woźniak K, Grela K, Trzaskowski B. Conformational flexibility of hoveyda-type and grubbs-type complexes bearing acyclic carbenes and its impact on their catalytic properties Organometallics. 34: 563-570. DOI: 10.1021/Om5006462 |
0.34 |
|
2015 |
Pump E, Leitgeb A, Kozłowska A, Torvisco A, Falivene L, Cavallo L, Grela K, Slugovc C. Variation of the Sterical Properties of the N-Heterocyclic Carbene Coligand in Thermally Triggerable Ruthenium-Based Olefin Metathesis Precatalysts/Initiators Organometallics. 34: 5383-5392. DOI: 10.1021/Acs.Organomet.5B00715 |
0.373 |
|
2015 |
Wappel J, Grudzień K, Barbasiewicz M, Michalak M, Grela K, Slugovc C. Initiation efficacy of halo-chelated cis-dichloro-configured ruthenium-based second-generation benzylidene complexes in ring-opening metathesis polymerization Monatshefte Fur Chemie. 146: 1153-1160. DOI: 10.1007/S00706-015-1494-8 |
0.346 |
|
2015 |
Szczepaniak G, Urbaniak K, Wierzbicka C, Kosiński K, Skowerski K, Grela K. Cover Picture: High-Performance Isocyanide Scavengers for Use in Low-Waste Purification of Olefin Metathesis Products (ChemSusChem 24/2015) Chemsuschem. 8: 4097-4097. DOI: 10.1002/Cssc.201501455 |
0.679 |
|
2015 |
Szczepaniak G, Urbaniak K, Wierzbicka C, Kosiński K, Skowerski K, Grela K. High-Performance Isocyanide Scavengers for Use in Low-Waste Purification of Olefin Metathesis Products Chemsuschem. 8: 4139-4148. DOI: 10.1002/Cssc.201500784 |
0.763 |
|
2014 |
Koz?owska A, Dranka M, Zachara J, Pump E, Slugovc C, Skowerski K, Grela K. Chelating ruthenium phenolate complexes: synthesis, general catalytic activity, and applications in olefin metathesis polymerization. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 14120-5. PMID 25204738 DOI: 10.1002/Chem.201403580 |
0.629 |
|
2014 |
Szczepaniak G, Kosiński K, Grela K. Towards "cleaner" olefin metathesis: Tailoring the NHC ligand of second generation ruthenium catalysts to afford auxiliary traits Green Chemistry. 16: 4474-4492. DOI: 10.1039/C4Gc00705K |
0.805 |
|
2014 |
Kajetanowicz A, Sytniczuk A, Grela K. Metathesis of renewable raw materials - Influence of ligands in the indenylidene type catalysts on self-metathesis of methyl oleate and cross-metathesis of methyl oleate with (Z)-2-butene-1,4-diol diacetate Green Chemistry. 16: 1579-1585. DOI: 10.1039/C3Gc42194E |
0.469 |
|
2014 |
Ablialimov O, Kedziorek M, Malinska M, Wozniak K, Grela K. Synthesis, structure, and catalytic activity of new ruthenium(II) indenylidene complexes bearing unsymmetrical N - heterocyclic carbenes Organometallics. 33: 2160-2171. DOI: 10.1021/Om4009197 |
0.453 |
|
2014 |
Smoleń M, Kȩdziorek M, Grela K. 2-Methyltetrahydrofuran: Sustainable solvent for ruthenium-catalyzed olefin metathesis Catalysis Communications. 44: 80-84. DOI: 10.1016/J.Catcom.2013.06.027 |
0.54 |
|
2014 |
Woźniak Ł, Zieliński G, Grela K. Olefin Metathesis Catalysts-A Tabular Review Olefin Metathesis: Theory and Practice. 573-585. DOI: 10.1002/9781118711613.oth1 |
0.45 |
|
2013 |
Ko?nik W, Grela K. Synthesis of functionalised N-heterocyclic carbene ligands bearing a long spacer and their use in olefin metathesis. Dalton Transactions (Cambridge, England : 2003). 42: 7463-7. PMID 23463014 DOI: 10.1039/C3Dt33010A |
0.543 |
|
2013 |
Klu?iar M, Grela K, Mauduit M. Ruthenium-based complexes containing a benzimidazolium tag covalently connected to N-heterocyclic carbene ligands: environmentally friendly catalysts for olefin metathesis transformations. Dalton Transactions (Cambridge, England : 2003). 42: 7354-8. PMID 23360984 DOI: 10.1039/C2Dt32856A |
0.569 |
|
2013 |
Torborg C, Szczepaniak G, Zieli?ski A, Mali?ska M, Wo?niak K, Grela K. Stable ruthenium indenylidene complexes with a sterically reduced NHC ligand. Chemical Communications (Cambridge, England). 49: 3188-90. PMID 23287841 DOI: 10.1039/C2Cc37514A |
0.776 |
|
2013 |
Wdowik T, Samoj?owicz C, Jawiczuk M, Mali?ska M, Wo?niak K, Grela K. Ruthenium nitronate complexes as tunable catalysts for olefin metathesis and other transformations. Chemical Communications (Cambridge, England). 49: 674-6. PMID 23223376 DOI: 10.1039/C2Cc37385H |
0.561 |
|
2013 |
Kajetanowicz A, Czaban J, Krishnan GR, Malińska M, Woźniak K, Siddique H, Peeva LG, Livingston AG, Grela K. Batchwise and continuous nanofiltration of POSS-tagged Grubbs-Hoveyda-type olefin metathesis catalysts. Chemsuschem. 6: 182-92. PMID 23086741 DOI: 10.1002/Cssc.201200466 |
0.595 |
|
2013 |
Gawin R, Pieczykolan M, Malińska M, Woźniak K, Grela K. Testing new ruthenium complexes bearing chiral 1,2,4-triazol-5-ylidene- ligands as catalysts for asymmetric olefin metathesis Synlett. 24: 1250-1254. DOI: 10.1055/S-0033-1338877 |
0.528 |
|
2013 |
Olszewski TK, Bieniek M, Skowerski K, Grela K. A new tool in the toolbox: Electron-withdrawing group activated -Ruthenium Catalysts for Olefin Metathesis Synlett. 24. DOI: 10.1055/S-0032-1318497 |
0.784 |
|
2013 |
Trzaskowski B, Grela K. Structural and mechanistic basis of the fast metathesis initiation by a six-coordinated ruthenium catalyst Organometallics. 32: 3625-3630. DOI: 10.1021/Om400233S |
0.586 |
|
2013 |
Zìukowska K, Szadkowska A, Trzaskowski B, Pazio A, Paì̈czek Ł, Woźniak K, Grela K. 3-bromopyridine as a sixth ligand in sulfoxide-based hoveyda complexes: A study on catalytic properties Organometallics. 32: 2192-2198. DOI: 10.1021/Om400064C |
0.43 |
|
2013 |
Jabłonka-Gronowska E, Witkowski B, Horeglad P, Gierczak T, Grela K. Testing the 1,1,3,3-tetramethyldisiloxane linker in olefin metathesis Comptes Rendus Chimie. 16: 566-572. DOI: 10.1016/J.Crci.2013.01.017 |
0.548 |
|
2013 |
Czaban J, Schertzer BM, Grela K. Low catalyst loadings in self-metathesis of 1-dodecene Advanced Synthesis and Catalysis. 355: 1997-2006. DOI: 10.1002/Adsc.201200713 |
0.451 |
|
2013 |
Czaban J, Torborg C, Grela K. Olefin Metathesis: From Academic Concepts to Commercial Catalysts Sustainable Catalysis: Challenges and Practices For the Pharmaceutical and Fine Chemical Industries. 163-214. DOI: 10.1002/9781118354520.ch09 |
0.485 |
|
2012 |
Barbasiewicz M, Michalak M, Grela K. A new family of halogen-chelated Hoveyda-Grubbs-type metathesis catalysts. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 14237-41. PMID 23033060 DOI: 10.1002/Chem.201202817 |
0.544 |
|
2012 |
Pietraszuk C, Rogalski S, Powa?a B, Mi?tkiewski M, Kubicki M, Spólnik G, Danikiewicz W, Wo?niak K, Pazio A, Szadkowska A, Koz?owska A, Grela K. Ruthenium-amido complexes: synthesis, structure, and catalytic activity in olefin metathesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 6465-9. PMID 22511306 DOI: 10.1002/Chem.201103973 |
0.472 |
|
2012 |
Skowerski K, Wierzbicka C, Szczepaniak G, Gułajski Ł, Bieniek M, Grela K. Easily removable olefin metathesis catalysts Green Chemistry. 14: 3264-3268. DOI: 10.1039/C2Gc36015B |
0.85 |
|
2012 |
Skowerski K, Szczepaniak G, Wierzbicka C, Gułajski Ł, Bieniek M, Grela K. Highly active catalysts for olefin metathesis in water Catalysis Science and Technology. 2: 2424-2427. DOI: 10.1039/C2Cy20320K |
0.845 |
|
2012 |
Ablialimov O, Kȩdziorek M, Torborg C, Malińska M, Woźniak K, Grela K. New ruthenium(II) indenylidene complexes bearing unsymmetrical N-heterocyclic carbenes Organometallics. 31: 7316-7319. DOI: 10.1021/Om300783G |
0.331 |
|
2012 |
Żukowska K, Szadkowska A, Pazio AE, Woźniak K, Grela K. Correction to Thermal Switchability of N-Chelating Hoveyda-type Catalyst Containing a Secondary Amine Ligand Organometallics. 31: 3814-3814. DOI: 10.1021/Om3003587 |
0.497 |
|
2012 |
Zukowska K, Szadkowska A, Pazio AE, Woźniak K, Grela K. Thermal switchability of N-chelating hoveyda-type catalyst containing a secondary amine ligand Organometallics. 31: 462-469. DOI: 10.1021/Om2011062 |
0.568 |
|
2012 |
Bek D, Gawin R, Grela K, Balcar H. Ruthenium metathesis catalyst bearing chelating carboxylate ligand immobilized on mesoporous molecular sieve SBA-15 Catalysis Communications. 21: 42-45. DOI: 10.1016/J.Catcom.2012.01.020 |
0.581 |
|
2012 |
Gawin R, Grela K. Synthesis of stable ruthenium olefin metathesis catalysts with mixed anionic ligands European Journal of Inorganic Chemistry. 1477-1484. DOI: 10.1002/Ejic.201101048 |
0.532 |
|
2012 |
Guidone S, Blondiaux E, Samojłowicz C, Gułajski Ł, Dziorek MK, Malińska M, Pazio A, Woźniak K, Grela K, Doppiu A, Cazin CSJ. Catalytic and structural studies of hoveyda-grubbs type pre-catalysts bearing modified ether ligands Advanced Synthesis and Catalysis. 354: 2734-2742. DOI: 10.1002/Adsc.201200385 |
0.6 |
|
2012 |
Cabrera J, Padilla R, Dehn R, Deuerlein S, Gułajski Ł, Chomiszczak E, Teles JH, Limbach M, Grela K. Olefin metathesis on a TLC Plate as a Tool for a High-Throughput Screening of Catalyst-Substrate Sets Advanced Synthesis and Catalysis. 354: 1043-1051. DOI: 10.1002/Adsc.201100863 |
0.546 |
|
2011 |
Samoj?owicz C, Bieniek M, Pazio A, Makal A, Wo?niak K, Poater A, Cavallo L, Wójcik J, Zdanowski K, Grela K. The doping effect of fluorinated aromatic solvents on the rate of ruthenium-catalysed olefin metathesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 12981-93. PMID 21956694 DOI: 10.1002/Chem.201100160 |
0.775 |
|
2011 |
Ahmadi A, McBride C, Freire JJ, Kajetanowicz A, Czaban J, Grela K. Force field parametrization and molecular dynamics simulation of flexible POSS-linked (NHC; phosphine) Ru catalytic complexes. The Journal of Physical Chemistry. A. 115: 12017-24. PMID 21932838 DOI: 10.1021/Jp2062332 |
0.406 |
|
2011 |
Samojłowicz C, Grela K. Olefin metathesis reactions of sulfur-containing alkenes and dienes Arkivoc. 2011: 82-103. DOI: 10.3998/Ark.5550190.0012.407 |
0.41 |
|
2011 |
Szadkowska A, Samojlowicz C, Grela K. Enhancement of ruthenium-catalyzed olefin metathesis reactions: Searching for new catalyst or new reaction conditions? Pure and Applied Chemistry. 83: 553-563. DOI: 10.1351/Pac-Con-10-09-10 |
0.589 |
|
2011 |
Pazio A, Makal A, Szadkowska A, Grela K, Woźniak K. Additional ligand in the Ru coordination sphere of Hoveyda-type catalysts. Part II Acta Crystallographica Section a Foundations of Crystallography. 67: C429-C430. DOI: 10.1107/S0108767311089215 |
0.494 |
|
2011 |
Shafi S, Kȩdziorek M, Grela K. Cross metathesis of N-allylamines and α,β-unsaturated carbonyl compounds: A one-pot synthesis of substituted pyrroles Synlett. 124-128. DOI: 10.1055/S-0030-1259083 |
0.466 |
|
2011 |
Bieniek M, Samojaowicz C, Sashuk V, Bujok R, Śledź P, Lugan N, Lavigne G, Arlt D, Grela K. Rational design and evaluation of upgraded Grubbs/Hoveyda olefin metathesis catalysts: Polyfunctional benzylidene ethers on the test bench Organometallics. 30: 4144-4158. DOI: 10.1021/Om200463U |
0.803 |
|
2011 |
Szadkowska A, Z̀ukowska K, Pazio AE, Woźniak K, Kadyrov R, Grela K. Ruthenium olefin metathesis catalysts containing six-membered sulfone and sulfonamide chelating rings Organometallics. 30: 1130-1138. DOI: 10.1021/Om101129B |
0.604 |
|
2011 |
Leitgeb A, Szadkowska A, Michalak M, Barbasiewicz M, Grela K, Slugovc C. Unequal siblings: Adverse characteristics of naphtalene-based hoveyda-type second generation initiators in ring opening metathesis polymerization Journal of Polymer Science, Part a: Polymer Chemistry. 49: 3448-3454. DOI: 10.1002/Pola.24776 |
0.307 |
|
2011 |
Samojłowicz C, Borré E, Mauduit M, Grela K. Microwave-assisted ruthenium-catalysed olefin metathesis in fluorinated aromatic hydrocarbons: A beneficial combination Advanced Synthesis and Catalysis. 353: 1993-2002. DOI: 10.1002/Adsc.201100053 |
0.427 |
|
2010 |
Poater A, Ragone F, Correa A, Szadkowska A, Barbasiewicz M, Grela K, Cavallo L. Mechanistic insights into the cis-trans isomerization of ruthenium complexes relevant to catalysis of olefin metathesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 14354-64. PMID 21053211 DOI: 10.1002/Chem.201001849 |
0.351 |
|
2010 |
Tzur E, Szadkowska A, Ben-Asuly A, Makal A, Goldberg I, Wo?niak K, Grela K, Lemcoff NG. Studies on electronic effects in O-, N- and S-chelated ruthenium olefin-metathesis catalysts. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 8726-37. PMID 20564287 DOI: 10.1002/Chem.200903457 |
0.522 |
|
2010 |
Pazio A, Makal A, Szadkowska A, Grela K, Woźniak K. Additional ligand in the Ru coordination sphere - the Hoveyda-type catalysts Acta Crystallographica Section a Foundations of Crystallography. 66: s269-s269. DOI: 10.1107/S0108767310093864 |
0.535 |
|
2010 |
Wdowik T, Samojowicz C, Jawiczuk M, Zarecki A, Grela K. Olefin cross-metathesis with 3-nitropropene Synlett. 2931-2935. DOI: 10.1055/S-0030-1259042 |
0.531 |
|
2010 |
Szadkowska A, Gstrein X, Burtscher D, Jarzembska K, Woźniak K, Slugovc C, Grela K. Latent thermo-switchable olefin metathesis initiators bearing a pyridyl-functionalized chelating carbene: Influence of the leaving group's rigidity on the catalyst's performance Organometallics. 29: 117-124. DOI: 10.1021/Om900857W |
0.827 |
|
2010 |
Grela K, Konopski L. 2-Substituted nitrones and isomeric hydroxylamines - obtained via aluminium amalgam reduction of nitro nitriles and ketones-a new access to convenient intermediates for nitroso carbonyl compounds preparation Tetrahedron. 66: 3608-3613. DOI: 10.1016/J.Tet.2010.03.023 |
0.406 |
|
2010 |
Grela K, Konopski L. A convenient synthesis of deuterium labeled tertiary aliphatic nitro ketones and nitriles - starting materials for preparation of deuterated cyclic nitrones, isomeric hydroxylamines, and corresponding C-nitroso compounds Tetrahedron. 66: 3614-3622. DOI: 10.1016/J.Tet.2010.03.022 |
0.33 |
|
2010 |
Gawin R, Czarnecka P, Grela K. Ruthenium catalysts bearing chelating carboxylate ligands: application to metathesis reactions in water Tetrahedron. 66: 1051-1056. DOI: 10.1016/J.Tet.2009.11.009 |
0.559 |
|
2010 |
Grela K, Michrowska A, Bieniek M, Sashuk V, Szadkowska A. ChemInform Abstract: Phosphine-Free EWG-Activated Ruthenium Olefin Metathesis Catalysts: Design, Preparation, and Applications Cheminform. 41. DOI: 10.1002/chin.201014246 |
0.771 |
|
2010 |
Grela K, Bieniek M. ChemInform Abstract: Highly Selective Cross-Metathesis with Phenyl Vinyl Sulfone Using the “Second Generation” Grubb′s Catalyst. Cheminform. 32: no-no. DOI: 10.1002/chin.200145106 |
0.479 |
|
2010 |
Gawin R, Grela K. Ruthenium catalysts bearing carboxylate ligand Nato Science For Peace and Security Series a: Chemistry and Biology. 57-69. |
0.485 |
|
2010 |
Gułajski L, Grela K. The influence of the anionic counter-ion on the activity of ammonium substituted Hoveyda-type olefin metathesis catalysts in aqueous media Nato Science For Peace and Security Series a: Chemistry and Biology. 49-56. |
0.388 |
|
2009 |
Samoj?owicz C, Bieniek M, Grela K. Ruthenium-based olefin metathesis catalysts bearing N-heterocyclic carbene ligands. Chemical Reviews. 109: 3708-42. PMID 19534492 DOI: 10.1021/Cr800524F |
0.752 |
|
2009 |
Burtscher D, Grela K. Aqueous olefin metathesis. Angewandte Chemie (International Ed. in English). 48: 442-54. PMID 18980239 DOI: 10.1002/Anie.200801451 |
0.765 |
|
2009 |
Gułajski Ł, Mauduit M, Grela K. Onium-tagged Ru complexes as universal catalysts for olefin metathesis reactions in various media Pure and Applied Chemistry. 81: 2001-2012. DOI: 10.1351/Pac-Con-08-10-13 |
0.589 |
|
2009 |
Szadkowska A, Makal A, Woźniak K, Kadyrov R, Grela K. Ruthenium Olefin metathesis initiators bearing chelating sulfoxide ligands Organometallics. 28: 2693-2700. DOI: 10.1021/Om801183G |
0.455 |
|
2009 |
Szadkowska A, Grela K. Design and application of latent olefin metathesis catalysts featuring S-chelating alkylidene ligands Nato Science For Peace and Security Series a: Chemistry and Biology. 289-302. DOI: 10.1007/978-90-481-3278-2-19 |
0.414 |
|
2009 |
Gawin R, Grela K. Ruthenium catalysts bearing O-Chelating carboxylate ligand: Potential chemo-switchable romp catalysts Nato Science For Peace and Security Series a: Chemistry and Biology. 279-288. DOI: 10.1007/978-90-481-3278-2-18 |
0.473 |
|
2009 |
Jarzembska K, Seal S, Woźniak K, Szadkowska A, Bieniek M, Grela K. X-ray photoelectron spectroscopy and reactivity studies of a series of ruthenium catalysts Chemcatchem. 1: 144-151. DOI: 10.1002/Cctc.200900052 |
0.695 |
|
2008 |
Samoj?owicz C, Bieniek M, Zarecki A, Kadyrov R, Grela K. The doping effect of fluorinated aromatic hydrocarbon solvents on the performance of common olefin metathesis catalysts: application in the preparation of biologically active compounds. Chemical Communications (Cambridge, England). 6282-4. PMID 19048129 DOI: 10.1039/B816567J |
0.732 |
|
2008 |
Sled? P, Mauduit M, Grela K. Olefin metathesis in ionic liquids. Chemical Society Reviews. 37: 2433-42. PMID 18949116 DOI: 10.1039/B711482F |
0.393 |
|
2008 |
Barbasiewicz M, Szadkowska A, Makal A, Jarzembska K, Wo?niak K, Grela K. Is the Hoveyda-Grubbs complex a vinylogous Fischer-type carbene? Aromaticity-controlled activity of ruthenium metathesis catalysts. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 9330-7. PMID 18770510 DOI: 10.1002/Chem.200800704 |
0.576 |
|
2008 |
Gu?ajski L, Michrowska A, Naroznik J, Kaczmarska Z, Rupnicki L, Grela K. A highly active aqueous olefin metathesis catalyst bearing a quaternary ammonium group. Chemsuschem. 1: 103-9. PMID 18605672 DOI: 10.1002/Cssc.200700111 |
0.594 |
|
2008 |
Grela K. The joy and challenge of small rings metathesis. Angewandte Chemie (International Ed. in English). 47: 5504-7. PMID 18553318 DOI: 10.1002/Anie.200801575 |
0.387 |
|
2008 |
Sashuk V, Samoj?owicz C, Szadkowska A, Grela K. Olefin cross-metathesis with vinyl halides. Chemical Communications (Cambridge, England). 2468-70. PMID 18491017 DOI: 10.1039/B801687A |
0.684 |
|
2008 |
Bieniek M, Michrowska A, Usanov DL, Grela K. In an attempt to provide a user's guide to the galaxy of benzylidene, alkoxybenzylidene, and indenylidene ruthenium olefin metathesis catalysts. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 806-18. PMID 18064624 DOI: 10.1002/Chem.200701340 |
0.848 |
|
2008 |
Szadkowska A, Grela K. Initiation at snail's pace: Design and applications of latent olefin metathesis catalysts featuring chelating alkylidene ligands Current Organic Chemistry. 12: 1631-1647. DOI: 10.2174/138527208786786264 |
0.418 |
|
2008 |
Michrowska A, Grela K. Quest for the ideal olefin metathesis catalyst Pure and Applied Chemistry. 80: 31-43. DOI: 10.1351/Pac200880010031 |
0.607 |
|
2008 |
Kirschning A, Gułajski L, Mennecke K, Meyer A, Busch T, Grela K. Highly active ammonium-tagged olefin-metathesis catalyst for simplified purification Synlett. 2692-2696. DOI: 10.1055/S-0028-1083512 |
0.563 |
|
2008 |
Gułajski Ł, Šledz̀ P, Lupa A, Grela K. Olefin metathesis in water using acoustic emulsification Green Chemistry. 10: 279-282. DOI: 10.1039/B719493E |
0.409 |
|
2008 |
Kirschning A, Harmrolfs K, Mennecke K, Messinger J, Schön U, Grela K. Homo- and heterogeneous Ru-based metathesis catalysts in cross-metathesis of 15-allylestrone-towards 17β-hydroxysteroid dehydrogenase type 1 inhibitors Tetrahedron Letters. 49: 3019-3022. DOI: 10.1016/J.Tetlet.2008.02.134 |
0.55 |
|
2007 |
Rix D, Caïjo F, Laurent I, Gulajski L, Grela K, Mauduit M. Highly recoverable pyridinium-tagged Hoveyda-Grubbs pre-catalyst for olefin metathesis. Design of the boomerang ligand toward the optimal compromise between activity and reusability. Chemical Communications (Cambridge, England). 3771-3. PMID 17851623 DOI: 10.1039/B705451C |
0.579 |
|
2007 |
Gawin R, Makal A, Wo?niak K, Mauduit M, Grela K. A dormant ruthenium catalyst bearing a chelating carboxylate ligand: in situ activation and application in metathesis reactions. Angewandte Chemie (International Ed. in English). 46: 7206-9. PMID 17661308 DOI: 10.1002/Anie.200701302 |
0.589 |
|
2007 |
Clavier H, Grela K, Kirschning A, Mauduit M, Nolan SP. Sustainable concepts in olefin metathesis. Angewandte Chemie (International Ed. in English). 46: 6786-801. PMID 17640026 DOI: 10.1002/Anie.200605099 |
0.576 |
|
2007 |
Czernuszewicz RS, Mody V, Zareba AA, Zaczek MB, Ga?ezowski M, Sashuk V, Grela K, Gryko DT. Solvent-dependent resonance Raman spectra of high-valent oxomolybdenum(V) tris[3,5-bis(trifluoromethyl)phenyl]corrolate. Inorganic Chemistry. 46: 5616-24. PMID 17547394 DOI: 10.1021/Ic070275G |
0.63 |
|
2007 |
Bieniek M, Michrowska A, Gułajski Ł, Grela K. A practical larger scale preparation of second-generation hoveyda-type catalysts Organometallics. 26: 1096-1099. DOI: 10.1021/Om0607651 |
0.736 |
|
2007 |
Gstrein X, Burtscher D, Szadkowska A, Barbasiewicz M, Stelzer F, Grela K, Slugovc C. Ruthenium quinoline and quinoxaline complexes: Thermally triggered initiators for ring opening metathesis polymerization Journal of Polymer Science, Part a: Polymer Chemistry. 45: 3494-3500. DOI: 10.1002/Pola.22083 |
0.747 |
|
2007 |
Barbasiewicz M, Bieniek M, Michrowska A, Szadkowska A, Makal A, Woźniak K, Grela K. Probing of the ligand anatomy: Effects of the chelating alkoxy ligand modifications on the structure and catalytic activity of ruthenium carbene complexes Advanced Synthesis and Catalysis. 349: 193-203. DOI: 10.1002/Adsc.200600478 |
0.664 |
|
2006 |
Bieniek M, Ko?oda D, Grela K. A highly selective synthesis of dialkenyl sulfones via cross-metathesis of divinyl sulfone. Organic Letters. 8: 5689-92. PMID 17134248 DOI: 10.1021/Ol061991+ |
0.663 |
|
2006 |
Bieniek M, Bujok R, Cabaj M, Lugan N, Lavigne G, Arlt D, Grela K. Advanced fine-tuning of grubbs/hoveyda olefin metathesis catalysts: a further step toward an optimum balance between antinomic properties. Journal of the American Chemical Society. 128: 13652-3. PMID 17044669 DOI: 10.1021/Ja063186W |
0.858 |
|
2006 |
Michrowska A, Mennecke K, Kunz U, Kirschning A, Grela K. A new concept for the noncovalent binding of a ruthenium-based olefin metathesis catalyst to polymeric phases: preparation of a catalyst on Raschig rings. Journal of the American Chemical Society. 128: 13261-7. PMID 17017807 DOI: 10.1021/Ja063561K |
0.609 |
|
2006 |
Grela K, Michrowska A, Bieniek M. Catalysts for new tasks: preparation and applications of tunable ruthenium catalysts for olefin metathesis. Chemical Record (New York, N.Y.). 6: 144-56. PMID 16795007 DOI: 10.1002/Tcr.20079 |
0.773 |
|
2006 |
Michrowska A, Gu?ajski ?, Grela K. A simple and practical phase-separation approach to the recycling of a homogeneous metathesis catalyst. Chemical Communications (Cambridge, England). 841-3. PMID 16479285 DOI: 10.1039/B517088E |
0.568 |
|
2006 |
Mennecke K, Grela K, Kunz U, Kirschning A. Immobilisation of the Grubbs III Olefin Metathesis Catalyst with Polyvinyl Pyridine (PVP). Cheminform. 37. DOI: 10.1055/S-2005-918958 |
0.509 |
|
2006 |
Michrowska A, Gułajski Ł, Kaczmarska Z, Mennecke K, Kirschning A, Grela K. A green catalyst for green chemistry: Synthesis and application of an olefin metathesis catalyst bearing a quaternary ammonium group Green Chemistry. 8: 685-688. DOI: 10.1039/B605138C |
0.622 |
|
2006 |
Barbasiewicz M, Szadkowska A, Bujok R, Grela K. Structure and activity peculiarities of ruthenium quinoline and quinoxaline complexes: Novel metathesis catalysts Organometallics. 25: 3599-3604. DOI: 10.1021/Om060091U |
0.746 |
|
2006 |
Sashuk V, Grela K. Synthetic and mechanistic studies on enyne metathesis: A catalyst influence Journal of Molecular Catalysis a: Chemical. 257: 59-66. DOI: 10.1016/J.Molcata.2006.05.033 |
0.789 |
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2006 |
Gułajski Ł, Michrowska A, Bujok R, Grela K. New tunable catalysts for olefin metathesis: Controlling the initiation through electronic factors Journal of Molecular Catalysis a: Chemical. 254: 118-123. DOI: 10.1016/J.Molcata.2005.12.049 |
0.79 |
|
2006 |
Rix D, Clavier H, Coutard Y, Gulajski L, Grela K, Mauduit M. Activated pyridinium-tagged ruthenium complexes as efficient catalysts for ring-closing metathesis Journal of Organometallic Chemistry. 691: 5397-5405. DOI: 10.1016/J.Jorganchem.2006.07.042 |
0.555 |
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2006 |
Bieniek M, Bujok R, Stepowska H, Jacobi A, Hagenkötter R, Arlt D, Jarzembska K, Makal A, Woźniak K, Grela K. New air-stable ruthenium olefin metathesis precatalysts derived from bisphenol S Journal of Organometallic Chemistry. 691: 5289-5297. DOI: 10.1016/J.Jorganchem.2006.07.041 |
0.848 |
|
2006 |
Vinokurov N, Michrowska A, Szmigielska A, Drzazga Z, Wójciuk G, Demchuk O, Grela K, Pietrusiewicz K, Butenschön H. Homo- and Cross-Olefin Metathesis Coupling of Vinylphosphane Oxides and Electron-Poor Alkenes: Access to P-Stereogenic Dienophiles Advanced Synthesis & Catalysis. 348: 931-938. DOI: 10.1002/Adsc.200505463 |
0.447 |
|
2006 |
Michrowska A, Gułajski Ł, Grela K. "Green" catalysts for green chemistry: New concepts in olefin metathesis catalysts separation and reuse Chimica Oggi. 24: 19-22. |
0.493 |
|
2005 |
Mennecke K, Grela K, Kunz U, Kirschning A. Immobilisation of the Grubbs III olefin metathesis catalyst with polyvinyl pyridine (PVP) Synlett. 2948-2952. DOI: 10.1055/s-2005-918958 |
0.507 |
|
2005 |
Mikus A, Sashuk V, Kedziorek M, Samojlowicz C, Ostrowski S, Grela K. Olefin and Enyne Cross-Metathesis — A New Tool for the Synthesis of Alkenyl-Substituted Azulenes. Cheminform. 36. DOI: 10.1055/S-2005-865242 |
0.708 |
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2005 |
Mikus A, Sashuk V, Kȩdziorek M, Samojłowicz C, Ostrowski S, Grela K. Olefin and enyne cross-metathesis - A new tool for the synthesis of alkenyl-substituted azulenes Synlett. 1142-1146. DOI: 10.1055/s-2005-865242 |
0.685 |
|
2004 |
Sashuk V, Ignatowska J, Grela K. A fine-tuned molybdenum hexacarbonyl/phenol initiator for alkyne metathesis. The Journal of Organic Chemistry. 69: 7748-51. PMID 15498008 DOI: 10.1021/Jo049158I |
0.776 |
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2004 |
Bujok R, Bieniek M, Masnyk M, Michrowska A, Sarosiek A, Stepowska H, Arlt D, Grela K. Ortho- and para-substituted Hoveyda-Grubbs carbenes. An improved synthesis of highly efficient metathesis initiators. The Journal of Organic Chemistry. 69: 6894-6. PMID 15387618 DOI: 10.1021/Jo049222W |
0.837 |
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2004 |
Michrowska A, Bujok R, Harutyunyan S, Sashuk V, Dolgonos G, Grela K. Nitro-substituted Hoveyda-Grubbs ruthenium carbenes: enhancement of catalyst activity through electronic activation. Journal of the American Chemical Society. 126: 9318-25. PMID 15281822 DOI: 10.1021/Ja048794V |
0.853 |
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2004 |
Sashuk V, Koszarna B, Winiarek P, Gryko DT, Grela K. The simple synthesis of stable A3- and trans-A 2B-molybdenum(V) corrolates Inorganic Chemistry Communications. 7: 871-875. DOI: 10.1016/J.Inoche.2004.05.010 |
0.69 |
|
2004 |
Michrowska A, Wawrzyniak P, Grela K. Synthesis of Macrocyclic Carbonates with Musk Odor by Ring-Closing Olefin Metathesis. Cheminform. 35. DOI: 10.1002/Ejoc.200300768 |
0.455 |
|
2003 |
Demchuk OM, Pietrusiewicz KM, Michrowska A, Grela K. Synthesis of substituted p-stereogenic vinylphosphine oxides by olefin cross-metathesis. Organic Letters. 5: 3217-20. PMID 12943391 DOI: 10.1021/Ol035011M |
0.471 |
|
2003 |
Michrowska A, Bieniek M, Kim M, Klajn R, Grela K. Cross-metathesis reaction of vinyl sulfones and sulfoxides Tetrahedron. 59: 4525-4531. DOI: 10.1016/S0040-4020(03)00682-3 |
0.826 |
|
2003 |
Grela K, Kim M. A Good Bargain: An Inexpensive, Air-Stable Ruthenium Metathesis Catalyst Derived from α-Asarone European Journal of Organic Chemistry. 2003: 963-966. DOI: 10.1002/Ejoc.200390151 |
0.82 |
|
2003 |
Grela K, Kim M. A Good Bargain: An Inexpensive, Air-Stable Ruthenium Metathesis Catalyst Derived from α-Asarone. Cheminform. 34. DOI: 10.1002/chin.200328069 |
0.43 |
|
2003 |
Grela K, Tryznowski M, Bieniek M. A PS-DES Immobilized Ruthenium Carbene: A Robust and Easily Recyclable Catalyst for Olefin Metathesis. Cheminform. 34. DOI: 10.1002/chin.200308059 |
0.5 |
|
2002 |
Grela K, Harutyunyan S, Michrowska A. A highly efficient ruthenium catalyst for metathesis reactions. Angewandte Chemie (International Ed. in English). 41: 4038-40. PMID 12412074 DOI: 10.1002/1521-3773(20021104)41:21<4038::Aid-Anie4038>3.0.Co;2-0 |
0.775 |
|
2002 |
Grela K, Ignatowska J. An improved catalyst for ring-closing alkyne metathesis based on molybdenum hexacarbonyl/2-fluorophenol. Organic Letters. 4: 3747-9. PMID 12375934 |
0.545 |
|
2002 |
Grela K, Tryznowski M, Bieniek M. A PS-DES immobilized ruthenium carbene: A robust and easily recyclable catalyst for olefin metathesis Tetrahedron Letters. 43: 9055-9059. DOI: 10.1016/S0040-4039(02)02283-9 |
0.768 |
|
2001 |
Fürstner A, Mathes C, Grela K. Concise total syntheses of epothilone A and C based on alkyne metathesis Chemical Communications. 1057-1059. DOI: 10.1039/B101669P |
0.588 |
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2001 |
Grela K, Bieniek M. Highly selective cross-metathesis with phenyl vinyl sulphone using the 'second generation' Grubbs' catalyst Tetrahedron Letters. 42: 6425-6428. DOI: 10.1016/S0040-4039(01)01269-2 |
0.765 |
|
2000 |
Fürstner A, Grela K. Ring-Closing Alkyne Metathesis: Application to the Stereoselective Total Synthesis of Prostaglandin E(2)-1,15-Lactone This work was supported by the Deutsche Forschungsgemeinschaft (Leibniz program) and the Fonds der Chemischen Industrie. K.G. thanks the Alexander von Humboldt Foundation for a fellowship. Angewandte Chemie (International Ed. in English). 39: 1234-1236. PMID 10767016 DOI: 10.1002/(Sici)1521-3773(20000403)39:7<1234::Aid-Anie1234>3.0.Co;2-V |
0.496 |
|
2000 |
Fürstner A, Grela K, Mathes C, Lehmann CW. Novel and Flexible Entries into Prostaglandins and Analogues Based on Ring Closing Alkyne Metathesis or Alkyne Cross Metathesis Journal of the American Chemical Society. 122: 11799-11805. DOI: 10.1021/Ja003119G |
0.645 |
|
2000 |
Fürstner A, Grela K. Ringschlussmetathese von Alkinen: Anwendung auf die stereoselektive Totalsynthese von Prostaglandin-E2-1,15-Lacton Angewandte Chemie. 112: 1292-1294. DOI: 10.1002/(Sici)1521-3757(20000403)112:7<1292::Aid-Ange1292>3.0.Co;2-G |
0.425 |
|
1998 |
Mąkosza M, Grela K. Preparation of Allylstannanes and Distannanes Using Zinc in Liquid Ammonia Synthetic Communications. 28: 2697-2702. DOI: 10.1080/00397919808004840 |
0.362 |
|
1998 |
Ma̧kosza M, Nieczypor P, Grela K. Convenient preparation of metals deposited on solid supports and their use in organic synthesis Tetrahedron. 54: 10827-10836. DOI: 10.1016/S0040-4020(98)00625-5 |
0.368 |
|
1997 |
Makosza M, Grela K. Convenient Preparation of 'High-Surface Sodium' in Liquid Ammonia: use in the Acyloin Reaction Synlett. 1997: 267-268. DOI: 10.1055/S-1997-763 |
0.329 |
|
1996 |
Mαkosza M, Grela K. A Mild and Simple Zinc-Promoted Barbier-Type Allylation of Aldehydes in Liquid Ammonia Synthetic Communications. 26: 2935-2940. DOI: 10.1080/00397919608005230 |
0.37 |
|
1996 |
Makosza M, Grela K, Fabianowski W. Active metals prepared in liquid ammonia. Zinc and tin-promoted synthesis of β-hydroxyesters, homoallylic and homopropargylic alcohols Tetrahedron. 52: 9575-9580. DOI: 10.1016/0040-4020(96)00494-2 |
0.364 |
|
1995 |
Mąkosza M, Grela K. Preparation of active zinc by reduction of zinc chloride with sodium in liquid ammonia and its use in the barbier reaction Tetrahedron Letters. 36: 9225-9226. DOI: 10.1016/0040-4039(95)01948-H |
0.341 |
|
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