☰

Marcin Kalek - Publications

Affiliations: 
2016- University of Warsaw, Poland 
Area:
Synthetic organic chemistry
Website:
http://kalekgroup.pl/members.html
Tree Info Similar researchers PubMed Report error

52 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Sarkar S, Kalek M. Metal-Free -Arylation of Phosphorothioate Diesters and Related Compounds with Diaryliodonium Salts. Organic Letters. PMID 36662120 DOI: 10.1021/acs.orglett.2c04310  0.674
2020 Perlinska AP, Kalek M, Christian T, Hou YM, Sulkowska JI. Mg-Dependent Methyl Transfer by a Knotted Protein: A Molecular Dynamics Simulation and Quantum Mechanics Study. Acs Catalysis. 10: 8058-8068. PMID 32904895 DOI: 10.1021/Acscatal.0C00059  0.361
2020 Kraszewski K, Tomczyk I, Drabinska A, Bienkowski K, Solarska R, Kalek M. Mechanism of Iodine(III)-Promoted Oxidative Dearomatizing Hydroxylation of Phenols: Evidence for Radical-Chain Pathway. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32608529 DOI: 10.1002/Chem.202002026  0.744
2020 Sarkar S, Ghosh MK, Kalek M. Synthesis of Pummerer’s ketone and its analogs by iodosobenzene-promoted oxidative phenolic coupling Tetrahedron Letters. 152459. DOI: 10.1016/J.Tetlet.2020.152459  0.551
2019 Ghosh MK, Rzymkowski J, Kalek M. Transition Metal-Free Aryl-Aryl Cross-Coupling: C-H Arylation of 2-Naphthols with Diaryliodonium Salts. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31162732 DOI: 10.1002/Chem.201902204  0.527
2019 Rajkiewicz AA, Wojciechowska N, Kalek M. N-Heterocyclic Carbene-Catalyzed Synthesis of Ynones via C–H Alkynylation of Aldehydes with Alkynyliodonium Salts—Evidence for Alkynyl Transfer via Direct Substitution at Acetylenic Carbon Acs Catalysis. 10: 831-841. DOI: 10.1021/Acscatal.9B04394  0.577
2018 Rajkiewicz AA, Kalek M. N-Heterocyclic Carbene-Catalyzed Olefination of Aldehydes with Vinyliodonium Salts To Generate α,β-Unsaturated Ketones. Organic Letters. PMID 29537278 DOI: 10.1021/Acs.Orglett.8B00447  0.797
2018 Kalek M, Ghosh M, Rajkiewicz A. Organocatalytic Group Transfer Reactions with Hypervalent Iodine­ Reagents Synthesis. 51: 359-370. DOI: 10.1055/S-0037-1609639  0.533
2017 Bäckvall JE, Qiu Y, Mendoza A, Posevins D, Himo F, Kalek M. Mechanistic Insight into Enantioselective Palladium-Catalyzed Oxidative Carbocyclization-Borylation of Enallenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29266429 DOI: 10.1002/Chem.201705239  0.712
2017 Kalek M, Himo F. Mechanism and Selectivity of Cooperatively-Catalyzed Meyer-Schuster Rearrangement/Tsuji-Trost Allylic Substitution. Evaluation of Synergistic Catalysis by Means of Combined DFT and Kinetics Simulations. Journal of the American Chemical Society. PMID 28675701 DOI: 10.1021/Jacs.7B01931  0.699
2017 Kalek M, Fu GC. Caution in the Use of Nonlinear Effects as a Mechanistic Tool for Catalytic Enantioconvergent Reactions: Intrinsic Negative Nonlinear Effects in the Absence of Higher-Order Species. Journal of the American Chemical Society. PMID 28276679 DOI: 10.1021/Jacs.7B01826  0.596
2016 Santoro S, Kalek M, Huang G, Himo F. Elucidation of Mechanisms and Selectivities of Metal-Catalyzed Reactions using Quantum Chemical Methodology. Accounts of Chemical Research. PMID 27082700 DOI: 10.1021/Acs.Accounts.6B00050  0.783
2015 Huang G, Kalek M, Liao RZ, Himo F. Mechanism, reactivity, and selectivity of the iridium-catalyzed C(sp(3))-H borylation of chlorosilanes. Chemical Science. 6: 1735-1746. PMID 29163873 DOI: 10.1039/C4Sc01592D  0.744
2015 Kalek M, Fu GC. Phosphine-Catalyzed Doubly Stereoconvergent γ-Additions of Racemic Heterocycles to Racemic Allenoates: The Catalytic Enantioselective Synthesis of Protected α,α-Disubstituted α-Amino Acid Derivatives. Journal of the American Chemical Society. 137: 9438-42. PMID 26192217 DOI: 10.1021/Jacs.5B05528  0.603
2015 Lee SY, Fujiwara Y, Nishiguchi A, Kalek M, Fu GC. Phosphine-catalyzed enantioselective intramolecular [3+2] annulations to generate fused ring systems. Journal of the American Chemical Society. 137: 4587-91. PMID 25815702 DOI: 10.1021/Jacs.5B01985  0.78
2013 Biswas S, Dahlstrand C, Watile RA, Kalek M, Himo F, Samec JS. Atom-efficient gold(I)-chloride-catalyzed synthesis of α-sulfenylated carbonyl compounds from propargylic alcohols and aryl thiols: substrate scope and experimental and theoretical mechanistic investigation. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 17939-50. PMID 24272980 DOI: 10.1002/Chem.201302485  0.671
2013 Huang G, Kalek M, Himo F. Mechanism and selectivity of rhodium-catalyzed 1:2 coupling of aldehydes and allenes. Journal of the American Chemical Society. 135: 7647-59. PMID 23659205 DOI: 10.1021/Ja4014166  0.687
2012 Kalek M, Himo F. Combining Meyer-Schuster rearrangement with aldol and Mannich reactions: theoretical study of the intermediate interception strategy. Journal of the American Chemical Society. 134: 19159-69. PMID 23106444 DOI: 10.1021/Ja307892C  0.698
2012 Jiménez-Halla JO, Kalek M, Stawinski J, Himo F. Computational study of the mechanism and selectivity of palladium-catalyzed propargylic substitution with phosphorus nucleophiles. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 12424-36. PMID 22890875 DOI: 10.1002/Chem.201201026  0.777
2011 Söderberg L, Lavén G, Kalek M, Stawinski J. 31P NMR and computational studies on stereochemistry of conversion of phosphoramidate diesters into the corresponding phosphotriesters. Nucleosides, Nucleotides & Nucleic Acids. 30: 552-64. PMID 21888546 DOI: 10.1080/15257770.2011.586009  0.785
2011 Kalek M, Stawinski J. ChemInform Abstract: Novel, Stereoselective and Stereospecific Synthesis of Allenylphosphonates and Related Compounds via Palladium-Catalyzed Propargylic Substitution. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201150164  0.693
2011 Kalek M, Stawinski J. Novel, Stereoselective and Stereospecific Synthesis of Allenylphosphonates and Related Compounds via Palladium-Catalyzed Propargylic Substitution Advanced Synthesis & Catalysis. 353: 1741-1755. DOI: 10.1002/Adsc.201100119  0.758
2010 Kalek M, Johansson T, Jezowska M, Stawinski J. Palladium-catalyzed propargylic substitution with phosphorus nucleophiles: efficient, stereoselective synthesis of allenylphosphonates and related compounds. Organic Letters. 12: 4702-4. PMID 20853904 DOI: 10.1021/Ol102121J  0.807
2010 Kalek M, Jezowska M, Stawinski J. Palladium-catalyzed propargylic substitution with phosphorus nucleophiles Synfacts. 2011: 307-307. DOI: 10.1055/S-0030-1259418  0.749
2010 Lavén G, Kalek M, Jezowska M, Stawinski J. Preparation of benzylphosphonates via a palladium(0)-catalyzed cross-coupling of H-phosphonate diesters with benzyl halides. Synthetic and mechanistic studies New Journal of Chemistry. 34: 967. DOI: 10.1039/B9Nj00585D  0.819
2010 Laven G, Kalek M, Jezowska M, Stawinski J. ChemInform Abstract: Preparation of Benzylphosphonates via a Palladium(0)-Catalyzed Cross-Coupling of H-Phosphonate Diesters with Benzyl Halides. Synthetic and Mechanistic Studies. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201040191  0.715
2010 Kalek M, Jezowska M, Stawinski J. ChemInform Abstract: Preparation of Arylphosphonates by Palladium(0)-Catalyzed Cross-Coupling in the Presence of Acetate Additives: Synthetic and Mechanistic Studies. Cheminform. 41. DOI: 10.1002/CHIN.201019169  0.697
2010 Kalek M, Stawinski J. ChemInform Abstract: Efficient Synthesis of Mono- and Diarylphosphinic Acids: A Microwave-Assisted Palladium-Catalyzed Cross-Coupling of Aryl Halides with Phosphinate. Cheminform. 41. DOI: 10.1002/CHIN.201014172  0.702
2009 Wallin R, Kalek M, Bartoszewicz A, Thelin M, Stawinski J. On the sulfurization of h-phosphonate diesters and phosphite triesters using elemental sulfur Phosphorus, Sulfur and Silicon and the Related Elements. 184: 908-916. DOI: 10.1080/10426500802715619  0.755
2009 Kalek M, Stawinski J. Efficient synthesis of mono- and diarylphosphinic acids: a microwave-assisted palladium-catalyzed cross-coupling of aryl halides with phosphinate Tetrahedron. 65: 10406-10412. DOI: 10.1016/J.Tet.2009.10.028  0.715
2009 Kalek M, Jezowska M, Stawinski J. Preparation of Arylphosphonates by Palladium(0)-Catalyzed Cross-Coupling in the Presence of Acetate Additives: Synthetic and Mechanistic Studies Advanced Synthesis & Catalysis. 351: 3207-3216. DOI: 10.1002/Adsc.200900590  0.734
2008 Kalek M, Ziadi A, Stawinski J. Microwave-assisted palladium-catalyzed cross-coupling of aryl and vinyl halides with H-phosphonate diesters. Organic Letters. 10: 4637-40. PMID 18808138 DOI: 10.1021/Ol801935R  0.757
2008 Kalek M, Bartoszewicz A, Stawinski J. Synthesis of nucleoside phosphorothio-, phosphorodithio- and phosphoroselenoate diesters via oxidative esterification of the corresponding H-phosphonate analogues. Nucleic Acids Symposium Series (2004). 285-6. PMID 18776365 DOI: 10.1135/Css200810219  0.788
2008 Bartoszewicz A, Kalek M, Stawinski J. The case for the intermediacy of monomeric metaphosphate analogues during oxidation of H-phosphonothioate, H-phosphonodithioate, and H-phosphonoselenoate monoesters: mechanistic and synthetic studies. The Journal of Organic Chemistry. 73: 5029-38. PMID 18507440 DOI: 10.1021/Jo8006072  0.752
2008 Kalek M, Benediktson P, Vester B, Wengel J. Identification of efficient and sequence specific bimolecular artificial ribonucleases by a combinatorial approach. Chemical Communications (Cambridge, England). 762-4. PMID 18478716 DOI: 10.1039/B712532A  0.608
2008 Deshmukh MV, Jones BN, Quang-Dang DU, Flinders J, Floor SN, Kim C, Jemielity J, Kalek M, Darzynkiewicz E, Gross JD. mRNA decapping is promoted by an RNA-binding channel in Dcp2. Molecular Cell. 29: 324-36. PMID 18280238 DOI: 10.1016/J.Molcel.2007.11.027  0.354
2008 Wierzchowski J, Pietrzak M, Stepinski J, Jemielity J, Kalek M, Bojarska E, Jankowska-Anyszka M, Davis RE, Darzynkiewicz E. Kinetics of C. elegans DcpS cap hydrolysis studied by fluorescence spectroscopy. Nucleosides, Nucleotides & Nucleic Acids. 26: 1211-5. PMID 18066754 DOI: 10.1080/15257770701527968  0.368
2008 Kalek M, Stawinski J. Synthetic studies on the P-C bond formation via a palladium-catalyzed cross-coupling reaction. Application to the synthesis of P-arylated nucleic acids Collection of Czechoslovak Chemical Communications. 10: 214-218. DOI: 10.1135/Css200810214  0.728
2008 Bartoszewicz A, Kalek M, Nilsson J, Hiresova R, Stawinski J. A new reagent system for efficient silylation of alcohols: Silyl chloride-N-methylimidazole-iodine Synlett. 0037-0040. DOI: 10.1055/S-2007-992379  0.769
2008 Kalek M, Stawinski J. Palladium-Catalyzed C−P Bond Formation: Mechanistic Studies on the Ligand Substitution and the Reductive Elimination. An Intramolecular Catalysis by the Acetate Group in PdIIComplexes Organometallics. 27: 5876-5888. DOI: 10.1021/Om800641N  0.706
2008 Bartoszewicz A, Kalek M, Stawinski J. Iodine-promoted silylation of alcohols with silyl chlorides. Synthetic and mechanistic studies Tetrahedron. 64: 8843-8850. DOI: 10.1016/J.Tet.2008.06.070  0.726
2008 Bartoszewicz A, Kalek M, Stawinski J. ChemInform Abstract: Iodine-Promoted Silylation of Alcohols with Silyl Chlorides. Synthetic and Mechanistic Studies. Cheminform. 39. DOI: 10.1002/CHIN.200852047  0.645
2008 Bartoszewicz A, Kalek M, Nilsson J, Hiresova R, Stawinski J. ChemInform Abstract: A New Reagent System for Efficient Silylation of Alcohols: Silyl Chloride-N-Methylimidazole-Iodine. Cheminform. 39. DOI: 10.1002/CHIN.200820041  0.65
2007 Kalek M, Madsen AS, Wengel J. Effective modulation of DNA duplex stability by reversible transition metal complex formation in the minor groove. Journal of the American Chemical Society. 129: 9392-400. PMID 17616191 DOI: 10.1021/Ja071076Z  0.605
2007 Darzynkiewicz ZM, Bojarska E, Kowalska J, Lewdorowicz M, Jemielity J, Kalek M, Stepinski J, Davis RE, Darzynkiewicz E. Interaction of human decapping scavenger with 5′ mRNA cap analogues: Structural requirements for catalytic activity Journal of Physics Condensed Matter. 19. DOI: 10.1088/0953-8984/19/28/285217  0.367
2007 Kalek M, Stawinski J. Pd(0)-Catalyzed Phosphorus−Carbon Bond Formation. Mechanistic and Synthetic Studies on the Role of the Palladium Sources and Anionic Additives Organometallics. 26: 5840-5847. DOI: 10.1021/Om700797K  0.66
2006 Kalek M, Jemielity J, Darzynkiewicz ZM, Bojarska E, Stepinski J, Stolarski R, Davis RE, Darzynkiewicz E. Enzymatically stable 5′ mRNA cap analogs: Synthesis and binding studies with human DcpS decapping enzyme Bioorganic and Medicinal Chemistry. 14: 3223-3230. PMID 16431118 DOI: 10.1016/J.Bmc.2005.12.045  0.409
2006 Grudzien E, Kalek M, Jemielity J, Darzynkiewicz E, Rhoads RE. Differential inhibition of mRNA degradation pathways by novel cap analogs. The Journal of Biological Chemistry. 281: 1857-67. PMID 16257956 DOI: 10.1074/Jbc.M509121200  0.335
2005 Stepinski J, Zuberek J, Jemielity J, Kalek M, Stolarski R, Darzynkiewicz E. Novel dinucleoside 5',5'-triphosphate cap analogues. Synthesis and affinity for murine translation factor eIF4E. Nucleosides, Nucleotides & Nucleic Acids. 24: 629-33. PMID 16248001 DOI: 10.1081/Ncn-200060103  0.496
2005 Kalek M, Jemielity J, Grudzien E, Zuberek J, Bojarska E, Cohen LS, Stepinski J, Stolarski R, Davis RE, Rhoads RE, Darzynkiewicz E. Synthesis and biochemical properties of novel mRNA 5' cap analogs resistant to enzymatic hydrolysis. Nucleosides, Nucleotides & Nucleic Acids. 24: 615-21. PMID 16247999 DOI: 10.1081/Ncn-200060091  0.378
2005 Kalek M, Jemielity J, Grudzien E, Zuberek J, Darzynkiewicz ZM, Bojarska E, Stępiński J, Stolarski R, Davis RE, Rhoads RE, Darżynkiewicz E. Synthesis and biochemical properties of the novel, enzymatically stable mRNA cap analogues with versatile potential applications Collection of Czechoslovak Chemical Communications. 7: 355-359. DOI: 10.1135/Css200507355  0.386
2005 Kalek M, Jemielity J, Stepinski J, Stolarski R, Darzynkiewicz E. A direct method for the synthesis of nucleoside 5′-methylenebis(phosphonate)s from nucleosides Tetrahedron Letters. 46: 2417-2421. DOI: 10.1016/J.Tetlet.2005.02.069  0.487
Show low-probability matches.