Publications

Found 415 results
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M
Makukhin, N.; Nosek, V.; Míšek, J. Development of a Ratiometric Fluorescent Probe with Two Reactive Sulfoxides for Monitoring the Activity of Methionine Sulfoxide Reductase A. Synthesis-Stuttgart 2018, 50 (4), 772-777 DOI: 10.1055/s-0036-1591888.
Makukhin, N.; Tretyachenko, V.; Moskovitz, J.; Míšek, J. A Ratiometric Fluorescent Probe for Imaging of the Activity of Methionine Sulfoxide Reductase A in Cells. Angewandte Chemie International Edition 2016, 55 (41), 12727-12730 DOI: 10.1002/anie.201605833.
Malkov, A. V.; Ramírez-López, P.; Bendová), L. Biedermann; Rulíšek, L.; Dufková, L.; Kotora, M.; Zhu, F.; Kočovský, P. On the mechanism of asymmetric allylation of aldehydes with allyltrichlorosi lanes catalyzed by QUINOX, a chiral lsoquinoline N-oxide. Journal of the American Chemical Society 2008, 130 (15), 5341-5348 DOI: 10.1021/ja711338q.
Malkov, A. V.; Westwater, M. - M.; Gutnov, A.; Ramírez-López, P.; Friscourt, F.; Kadlcikova, A.; Hodačová, J.; Rankovic, Z.; Kotora, M.; Kočovský, P. New pyridine N-oxides as chiral organocatalysts in the asymmetric allylation of aromatic aldehydes. Tetrahedron 2008, 64 (49), 11335-11348 DOI: 10.1016/j.tet.2008.08.084.
Malkov, A. V.; Kysilka, O.; Edgar, M.; Kadlcikova, A.; Kotora, M.; Kočovský, P. A Novel Bifunctional Allyldisilane as a Triple Allylation Reagent in the Stereoselective Synthesis of Trisubstituted Tetrahydrofurans. Chemistry - A European Journal 2011, 17 (26), 7162-7166 DOI: 10.1002/chem.201100513.
Malnuit, V.; Smolen, S.; Tichý, M.; Slavětínská, L. Poštová; Hocek, M. Synthesis of Cyclic and Acyclic Nucleoside Phosphonates and Sulfonamides Derived from 6-(Thiophen-2-yl)-7-fluoro-7-deazapurine. European Journal of Organic Chemistry 2019, 2019 (31-32), 5409-5423 DOI: 10.1002/ejoc.201900509.
Malnuit, V.; Slavětínská, L. Poštová; Nauš, P.; Džubák, P.; Hajdúch, M.; Stolaříková, J.; Snášel, J.; Pichová, I.; Hocek, M. 2-Substituted 6-(Het)aryl-7-deazapurine Ribonucleosides: Synthesis, Inhibition of Adenosine Kinases, and Antimycobacterial Activity. ChemMedChem 2015, 10 (6), 1079-1093 DOI: 10.1002/cmdc.201500081.
Markos, A.; Voltrova, S.; Motornov, V.; Tichy, D.; Klepetářová, B.; Beier, P. Stereoselective Synthesis of (Z)-beta-Enamido Triflates and Fluorosulfonates from N-Fluoroalkylated Triazoles. Chemistry-a European Journal 2019, 25 (32), 7640-7644 DOI: 10.1002/chem.201901632.
Mateus, M. Alexandre; Kunák, D.; Rýček, L. Synthesis and Structure Confirmation of Selagibenzophenone C. European Journal of Organic Chemistry 2022, 2022 (11), nestránkováno.
Mateus, M. Alexandre; Lapinskaite, R.; Malatinec, Š.; Rýček, L. Cross-Coupling as a Key Step in the Synthesis and Structure Revision of the Natural Products Selagibenzophenones A and B. Catalysts [online] 2021, 11 (6), nestránkováno.
Matoušová, E.; Koukal, P.; Formánek, B.; Kotora, M. Enantioselective Synthesis of the Unsaturated Fragment of Callyspongiolide. Organic Letters 2016, 18 (21), 5656-5659 DOI: 10.1021/acs.orglett.6b02897.
Matoušová, E.; Růžička, A.; Kuneš, J.; Králová, J.; Pour, M. TFP as a ligand in Au(i)-catalyzed dihydropyran synthesis. Unprecedented rearrangement of dihydropyrans into cyclopentenones. Chemical Communications 2011, 47 (33), 9390 DOI: 10.1039/c1cc13525b.
Matoušová, E.; Gyepes, R.; Císařová, I.; Kotora, M. [2+2+2]-Cyclotrimerization of 1-Cyclopropyl-1,6-diynes with Alkynes: Formation of Cyclopropylarenes. Advanced Synthesis & Catalysis 2016, 358 (2), 254-267 DOI: 10.1002/adsc.201500851.
Matyašovský, J.; Pohl, R.; Hocek, M. 2-Allyl- and Propargylamino-dATPs for Site-Specific Enzymatic Introduction of a Single Modification in the Minor Groove of DNA. Chemistry-a European Journal 2018, 24 (56), 14938-14941 DOI: 10.1002/chem.201803973.
Matyašovský, J.; Perlíková, P.; Malnuit, V.; Pohl, R.; Hocek, M. 2-Substituted dATP Derivatives as Building Blocks for Polymerase-Catalyzed Synthesis of DNA Modified in the Minor Groove. Angewandte Chemie International Edition 2016, 55 (51), 15856-15859 DOI: 10.1002/anie.201609007.
Ménová, P.; Hocek, M. Preparation of short cytosine-modified oligonucleotides by nicking enzyme amplification reaction. Chemical Communications 2012, 48 (55), 6921 DOI: 10.1039/c2cc32930a.
Ménová, P.; Cahová, H.; Plucnara, M.; Havran, L.; Fojta, M.; Hocek, M. Polymerase synthesis of oligonucleotides containing a single chemically modified nucleobase for site-specific redox labelling. Chemical Communications 2013, 49 (41), 4652 DOI: 10.1039/c3cc41438h.
Ménová, P.; Raindlová, V.; Hocek, M. Scope and Limitations of the Nicking Enzyme Amplification Reaction for the Synthesis of Base-Modified Oligonucleotides and Primers for PCR. Bioconjugate Chemistry 2013, 24 (6), 1081-1093 DOI: 10.1021/bc400149q.
Ménová, P.; Dziuba, D.; Güixens-Gallardo, P.; Jurkiewicz, P.; Hof, M.; Hocek, M. Fluorescence Quenching in Oligonucleotides Containing 7-Substituted 7-Deazaguanine Bases Prepared by the Nicking Enzyme Amplification Reaction. Bioconjugate Chemistry 2015, 26 (2), 361-366 DOI: 10.1021/acs.bioconjchem.5b00006.
Merta, A.; Votruba, I.; Jindrich, J.; Holy, A.; Cihlar, T.; Rosenberg, I.; Otmar, M.; Herve, T. Y. Phosphorylation of 9-(2-phosphonomethoxyethyl)adenine and 9-(S)-(3-hydroxy-2-phosphonomethoxypropyl)adenine by AMP (dAMP) kinase from L1210 cells. Biochemical Pharmacology 1992, 44 (10), 2067-2077 DOI: 10.1016/0006-2952(92)90110-5.
Mikušek, J.; Jansa, P.; Jagtap, P. R.; Vasicek, T.; Císařová, I.; Matoušová, E. Enantioselective Synthesis of All-Carbon Quaternary Centers Structurally Related to Amaryllidaceae Alkaloids. Chemistry-a European Journal 2018, 24 (40), 10069-10072 DOI: 10.1002/chem.201802493.
Mikušek, J.; Matouš, P.; Matoušová, E.; Janoušek, M.; Kuneš, J.; Pour, M. Substrate Control in the Gold(I)-Catalyzed Cyclization of β - Propargylamino Acrylic Esters and Further Transformations of the Resultant Dihydropyridines. Advanced Synthesis & Catalysis 2016, 358 (18), 2912-2922 DOI: 10.1002/adsc.201600412.
Motloch, P.; Blahut, J.; Císařová, I.; Roithová, J. X-ray characterization of triphenylphosphine-gold(I) olefin pi-complexes and the revision of their stability in solution. Journal of Organometallic Chemistry 2017, 848, 114-117 DOI: 10.1016/j.jorganchem.2017.07.011.
Motloch, P.; Valterová, I.; Kotora, M. Enantioselective Allylation of Thiophene-2-carbaldehyde: Formal Total Synthesis of Duloxetine. Advanced Synthesis & Catalysis 2014, 356 (1), 199-204 DOI: 10.1002/adsc.201300849.
Murphy, B.; Šnajdr, I.; Machara, A.; Endoma-Arias, M. Ann A.; Stamatatos, T. C.; D. Cox, P.; Hudlicky, T. Conversion of Thebaine to Oripavine and Other Useful Intermediates for the Semisynthesis of Opiate-Derived Agents: Synthesis of Hydromorphone. Advanced Synthesis & Catalysis 2014, 356 (11-12), 2679-2687 DOI: 10.1002/adsc.201400445.
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