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 |
0.364 |
|
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 |
0.733 |
|
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 |
0.549 |
|
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 |
0.526 |
|
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 |
0.579 |
|
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 |
0.789 |
|
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 |
0.537 |
|
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 |
0.711 |
|
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 |
0.7 |
|
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 |
0.598 |
|
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 |
0.781 |
|
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 |
0.743 |
|
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 |
0.602 |
|
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 |
0.776 |
|
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 |
0.667 |
|
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 |
0.688 |
|
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 |
0.7 |
|
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 |
0.739 |
|
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 |
0.777 |
|
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 |
0.601 |
|
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 |
0.695 |
|
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 |
0.805 |
|
2010 |
Kalek M, Jezowska M, Stawinski J. Palladium-catalyzed propargylic substitution with phosphorus nucleophiles Synfacts. 2011: 307-307. DOI: 10.1055/S-0030-1259418 |
0.682 |
|
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 |
0.807 |
|
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 |
0.623 |
|
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 |
0.599 |
|
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 |
0.606 |
|
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 |
0.751 |
|
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 |
0.635 |
|
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 |
0.662 |
|
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 |
0.691 |
|
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 |
0.752 |
|
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 |
0.71 |
|
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 |
0.358 |
|
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 |
0.373 |
|
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 |
0.655 |
|
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 |
0.734 |
|
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 |
0.629 |
|
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 |
0.675 |
|
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 |
0.536 |
|
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 |
0.543 |
|
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 |
0.606 |
|
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 |
0.372 |
|
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 |
0.567 |
|
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 |
0.411 |
|
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 |
0.339 |
|
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 |
0.495 |
|
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 |
0.379 |
|
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 |
0.385 |
|
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 |
0.485 |
|
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