Publications

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E
Hanzlová, E.; Váňa, J.; Shaffer, C. J.; Roithová, J.; Martinů, T. Evidence for the Cyclic CN 2 Carbene in the Gas Phase. Organic Letters 2014, 16 (20), 5482-5485 DOI: 10.1021/ol5027602.
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.
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.; 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.
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.
Dračínský, M.; Drastík, M.; Kašpar, M.; Klepetářová, B.; Kronenberger, T.; Kudová, E.; Mičuda, S.; Pávek, P.; Štefela, A. (E)-7-Ethylidene-lithocholic Acid (7-ELCA) Is a Potent Dual Farnesoid X Receptor (FXR) Antagonist and GPBAR1 Agonist Inhibiting FXR-Induced Gene Expression in Hepatocytes and Stimulating Glucagon-like Peptide-1 Secretion From Enteroendocrine Cells. Frontiers in Pharmacology 2021, 12 (August), nestránkováno.
D
Machara, A.; Endoma-Arias, M. Ann A.; Císařová, I.; D. Cox, P.; Hudlicky, T. Direct Synthesis of Noroxymorph­one from Thebaine: Unusual Ce IV Oxidation of a Methoxydiene-Iron Complex to an Enone-γ-Nitrate. European Journal of Organic Chemistry 2016, 2016 (8), 1500-1503 DOI: 10.1002/ejoc.201600153.
Machara, A.; D. Cox, P.; Hudlicky, T. Direct Synthesis of Naltrexone by Palladium-Catalyzed N -Demethylation/Acylation of Oxymorphone: The Benefit of CH Activation and the Intramolecular Acyl Transfer from C-14 Hydroxy. Advanced Synthesis & Catalysis 2012, 354 (14-15), 2713-2718 DOI: 10.1002/adsc.201200677.
A. Downey, M.; Richter, C.; Pohl, R.; Mahrwald, R.; Hocek, M. Direct One-Pot Synthesis of Nucleosides from Unprotected or 5-O-Monoprotected D-Ribose. Organic Letters 2015, 17 (18), 4604-4607 DOI: 10.1021/acs.orglett.5b02332.
Banwell, M. G.; Buckler, J. N.; Jackson, C. J.; Lan, P.; Ma, X.; Matoušová, E.; Nugent, J. Devising New Syntheses of the Alkaloid Galanthamine, a Potent and Clinically Deployed Inhibitor of Acetylcholine Esterase; Elsevier, 2015; Vol. 11, pp 29-50.
Banwell, M. G.; Buckler, J. N.; Jackson, C. J.; Lan, P.; Ma, X.; Matoušová, E.; Nugent, J. Devising New Syntheses of the Alkaloid Galanthamine, a Potent and Clinically Deployed Inhibitor of Acetylcholine Esterase; Elsevier, 2015; Vol. 11, pp 29-50.
Kasireddy, S. Reddy; Míšek, J.; Nosek, V.; Tarallo, V. Development of a simple high-throughput assay for directed evolution of enantioselective sulfoxide reductases. Chemical Communications 2020, 56 (40), 5386-5388 DOI: 10.1039/d0cc01660h.
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.; 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.
Čihák, M.; Hurný, D.; Malečková, A.; Štuka, Č.; Tonar, Z.; Vejražka, M. "Desatero" akademického pedagoga. https://karlovkaonline.cz/wp-content/uploads/2021/04/UK_fond-desatero_www.pdf, 2021.
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