Publications
Found 157 results
Author Title [ Type] Year Filters: First Letter Of Last Name is P [Clear All Filters]
Extension of the Library of Biologically Active γ-Alkylidene Butenolides. Synthesis 2008, 2008 (21), 3465-3472 DOI: 10.1055/s-0028-1083181.
Enantioselective Cyclopropanation of 4-Nitroisoxazole Derivatives. Advanced Synthesis and Catalysis 2020, 362 (13), 2597-2603 DOI: 10.1002/adsc.202000231.
Electrochemical behaviour of 2,4-dinitrophenylhydrazi(o)ne as multi-redox centre DNA label at mercury meniscus modified silver solid amalgam electrode. Electrochimica Acta 2014, 126, 122-131 DOI: 10.1016/j.electacta.2013.09.147.
(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.
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.
Direct C–H sulfenylation of purines and deazapurines. Organic & Biomolecular Chemistry 2013, 11 (31), 5189 DOI: 10.1039/c3ob40881g.
Determination of sensoric parameters of porous silicon in sensing of organic vapors. Materials Science and Engineering: C 2002, 19 (1-2), 251-254 DOI: 10.1016/S0928-4931(01)00394-0.
Determination of cyclodextrins and their derivatives by capillary electrophoresis with indirect UV and conductivity detection. Fresenius Journal of Analytical Chemistry 2001, 369 (7-8), 666-669 DOI: 10.1007/s002160100721.
Determination of cyclodextrin content using periodate oxidation by capillary electrophoresis. Journal of Chromatography A 2000, 891 (1), 201-206 DOI: 10.1016/S0021-9673(00)00628-2.
Cyclodextrin-based Schiff base pro-fragrances: Synthesis and release studies. Beilstein Journal of Organic Chemistry 2022, 18 (September), 1346-1354.
Cross-metathesis reaction of α- and β-vinyl C -glycosides with alkenes. Beilstein Journal of Organic Chemistry 2015, 11, 1392-1397 DOI: 10.3762/bjoc.11.150.
Cross-Coupling Reaction of Saccharide-Based Alkenyl Boronic Acids with Aryl Halides: The Synthesis of Bergenin. Chemistry - A European Journal 2014, 20 (15), 4414-4419 DOI: 10.1002/chem.201304304.
Cross-Coupling Reaction of Saccharide-Based Alkenyl Boronic Acids with Aryl Halides: The Synthesis of Bergenin. Chemistry - A European Journal 2014, 20 (15), 4414-4419 DOI: 10.1002/chem.201304304.
Copper-mediated arylsulfanylations and arylselanylations of pyrimidine or 7-deazapurine nucleosides and nucleotides. Org. Biomol. Chem. 2016, 14 (42), 10018-10022 DOI: 10.1039/C6OB01917J.
A complete series of 6-deoxy-monosubstituted tetraalkylammonium derivatives of α-, β-, and γ-cyclodextrin with 1, 2, and 3 permanent positive charges. Beilstein Journal of Organic Chemistry 2014, 10, 1390-1396 DOI: 10.3762/bjoc.10.142.
Comparison of Association Constants of Cyclodextrins and Their tert-Butyl Derivatives With Halogenbenzoic Acids and Acridine Derivatives. Molecules 2001, 6 (3), 221-229 DOI: 10.3390/60300221.
Cobalt‐Induced Synthesis of 6‐(Pyridin‐2‐yl)purines by Microwave‐Enhanced [2+2+2] Cyclotrimerization. European Journal of Organic Chemistry 2008, 2008 (19), 3335-3343 DOI: 10.1002/ejoc.200800205.
Chromatographic Characterization of a New Cationic β-CD Based Stationary Phase Prepared by Dynamic Coating. Chromatographia 2016, 79 (9-10), 529-536 DOI: 10.1007/s10337-016-3050-z.
Chromatographic Characterization of a New Cationic β-CD Based Stationary Phase Prepared by Dynamic Coating. Chromatographia 2016, 79 (9-10), 529-536 DOI: 10.1007/s10337-016-3050-z.
Chloroacetamide-Linked Nucleotides and DNA for Cross-Linking with Peptides and Proteins. Bioconjugate Chemistry 2016, 27 (9), 2089-2094 DOI: 10.1021/acs.bioconjchem.6b00342.
Chemically modified glycogens: How they influence formation of amyloid fibrils?. Soft Matter 2021, 17 (6), 1614-1627.
Chelating Polymers for Hereditary Hemochromatosis Treatment. Macromolecular Bioscience 2020, 20 (12), nestránkováno DOI: 10.1002/mabi.202000254.
Chelating Polymers for Hereditary Hemochromatosis Treatment. Macromolecular Bioscience 2020, 20 (12), nestránkováno DOI: 10.1002/mabi.202000254.
Chelating Polymers for Hereditary Hemochromatosis Treatment. Macromolecular Bioscience 2020, 20 (12), nestránkováno DOI: 10.1002/mabi.202000254.
C-H Trifluoromethylations of 1,3-Dimethyluracil and Reactivity of the Products in C-H Arylations. HETEROCYCLES 2014, 89 (5), 1159 DOI: 10.3987/COM-14-12958.