Originalbeiträge

  • P. Seidel, A. Schwarzer, M. Mazik
    Crystal structure of 9,9-diethylfluorene-2,4,7-tricarbaldehyde
    Acta Crystallogr., Sect. E 2021, 77, 1029-1032. (DOI)
  • F. Amrhein, M. Mazik
    Compounds Combining a Macrocyclic Building Block and Flexible Side-Arms as Carbohydrate Receptors: Syntheses and Structure-Binding Activity Relationship Studies
    Eur. J. Org. Chem. 2021, im Druck. (DOI)
  • M. Stapf, B. Leibiger, A. Schwarzer, M. Mazik
    Crystal structures of 2-[3,5-bis(bromomethyl)-2,4,6-triethylbenzyl] isoindoline-1,3-dione and 2-{5-(bromomethyl)-3-[(1,3-dioxoisoindolin-2- yl)methyl]-2,4,6-triethylbenzyl}isoindoline-1,3-dione
    Acta Crystallogr., Sect. E 2021, 77, 919-923. (DOI)
  • L. Köhler, C. Hübler, W. Seichter, M. Mazik
    Binding modes of methyl α-d-glucopyranoside to an artificial receptor in crystalline complexes
    RSC Advances 2021, 11(36), 22221–22229. (DOI)
  • P. Seidel, W. Seichter, A. Schwarzer, M. Mazik
    Fluorene derivatives bearing two to seven phthalimidomethyl groups: Syntheses, crystal structures and conversion to amines
    Eur. J. Org. Chem. 2021, 2901-2914. (DOI)
  • F. Amrhein, A. Schwarzer, M. Mazik
    Crystal structure of a methanol solvate of a macrocycle bearing two flexible side-arms
    Acta Crystallogr., Sect. E 2021, 77, 233-236. (DOI)
  • J. Lerchner, M.R. Sartori, P.O. Volpe, S. Förster, M. Mazik, A.E. Vercesi, F. Mertens
    Segment fusion chip calorimetry: a new method for the investigation of fast reactions
    J. Therm. Anal. Calorim. 2021, im Druck. (DOI)
  • L. Köhler, W. Seichter, M. Mazik
    Complexes formed between artificial receptors and β‐glucopyranoside in the crystalline state
    Eur. J. Org. Chem. 2020, 7023-7034. (DOI)
  • P. Seidel, M. Mazik
    Syntheses of Acyclic and Macrocyclic Compounds Derived from 9,9‐Diethylfluorene (Part I)
    ChemistryOpen 2020, 9(11), 1202-1213. (DOI)
  • M. Stapf, W. Seichter, M. Mazik
    Crystal structures of monohydrate and methanol solvate compounds of {1-[(3,5-bis{[(4,6-dimethylpyridin-2-yl)amino]methyl}-2,4,6-triethylbenzyl)amino]cyclopentyl}methanol
    Acta Crystallogr., Sect. E 2020, 76, 1679-1683. (DOI)
  • M. Stapf, W. Seichter, M. Mazik
    Cycloalkyl Groups as Subunits of Artificial Carbohydrate Receptors: Effect of Ring Size of the Cycloalkyl Unit on the Receptor Efficiency
    Eur. J. Org. Chem. 2020, 4900-4915. (DOI)
  • S. Kaiser, C. Geffert, M. Mazik
    Purine unit as a building block of artificial receptors designed for the recognition of carbohydrates
    Eur. J. Org. Chem. 2019, 7555- 7562. (DOI)
  • M. M. Schulze, R. Löwe, R. Pollex, M. Mazik
    Structure-extractability relationships for substituted 8-hydroxyquinolines: solvent extraction of indium ions from acidic aqueous media
    Monatsh. Chem. 2019, 150, 983-990. (DOI)
  • P. Seidel, A. Schwarzer, M. Mazik
    Fluorene Derivatives Bearing Halogenomethyl Groups: Synthesis, Molecular Structures, and Halogen/Hydrogen Bonding Patterns in the Crystalline State
    Eur. J. Org. Chem. 2019, 1493-1502. (DOI)
  • M. M. Schulze, N. Koch, W. Seichter, M. Mazik
    Crystalline Ammonium Complexes of Trimethyl- and Triethylbenzene-Based Tripodal Compounds Bearing Pyrazole and Indazole Groups
    Eur. J. Org. Chem. 2018, 4317-4330. (DOI)
  • R. Rosin, W. Seichter, A. Schwarzer, M. Mazik
    1,8-naphthyridine carbaldehydes and their methyl-substituted precursors: synthesis, molecular structures, supramolecular motifs and trapped water clusters
    Eur. J. Org. Chem. 2017, 6038-6051. (DOI)
  • R. Rosin, W. Seichter, M. Mazik
    Crystal structures of the dioxane hemisolvates of N-(7-bromomethyl-1,8-naphthyridin-2-yl)acetamide and bis[N-(7-dibromomethyl-1,8-naphthyridin-2-yl)acetamide]
    Acta Crystallgr., Sect. E 2017, 73, 1409-1413. (DOI)
  • M. M. Schulze, A. Schwarzer, M. Mazik
    Conformations of benzene-based tripodal isatin-bearing compounds in the crystalline state
    CrystEngComm 2017, 19, 4003-4016. (DOI)
  • N. Koch, W. Seichter, M. Mazik
    Trimethyl-, triethyl- and trimethoxybenzene-based tripodal compounds bearing pyrazole groups: conformations and halogen-/hydrogen-bond patterns in the crystalline state
    CrystEngComm 2017, 19, 3817-3833. (DOI)
  • F. Amrhein, J. Lippe, M. Mazik
    Carbohydrate receptors combining both a macrocyclic building block and flexible side arms as recognition units: binding properties of compounds with CH2OH groups as side arms
    Org. Biomol. Chem. 201614, 10648-10659. (DOI)
  • N. Koch, W. Seichter, M. Mazik
    Compounds Based on a Triethyl- or Trimethoxybenzene Scaffold Bearing Pyrazole, Pyridine, and Pyrimidine Groups: Syntheses and Representative Binding Studies towards Carbohydrates
    Synthesis 2016, 48(17), 2757-2767. (DOI)
  • M. Stapf, W. Seichter, M. Mazik
    Unique hydrogen-bonded complex of hydronium and hydroxide ions
    Chem. Eur. J. 2015, 21, 6350-6354. (DOI)
  • J. Lippe, M. Mazik
    Carbohydrate receptors combining both a macrocyclic building block and flexible side-arms as recognition units: design, syntheses and binding studies
    J. Org. Chem. 2015, 80, 1427-1439. (DOI)
  • J. Lippe, W. Seichter, M. Mazik
    Improved binding affinity and interesting selectivities of aminopyrimidine-bearing carbohydrate receptors in comparison with their aminopyridine analogues
    Org. Biomol. Chem. 2015, 13, 11622-11632. (DOI)
  • N. Koch, W. Seichter, M. Mazik
    Hexapodal pyrazole-based receptors: Complexes with ammonium ions and solvent molecules in the solid state
    Tetrahedron 2015, 71, 8965-8974. (DOI)
  • U. Schmidt, M. Mazik
    N,N’,N’’,N’’’-Tetrakis(5,7-dimethyl-1,8-naphthyridine-2-yl)-3,3’,5,5’-diphenylmethanetetracarboxamide
    Molbank 2015, 2015, M844. (DOI)
  • U. Schmidt, M. Stapf, M. Mazik
    N,N’,N’’- Tris[(5-methoxyindol-3-yl)ethyl]benzene-1,3,5-tricarboxamide
    Molbank 2015, 2015, M850. (DOI)
  • N. Koch, J.-R. Rosien, M. Mazik
    Synthesis of compounds based on a dimesitylmethane scaffold and representative binding studies showing di- vs. monosaccharide preference
    Tetrahedron 2014, 70, 8758-8767. (DOI)
  • N. Koch, W. Seichter, M. Mazik
    2-{2,4,6-Tris(bromomethyl)-3,5-bis-[(1,3-dioxoisoindolin-2-yl)methyl]benzyl}isoindoline-1,3-dione toluene monosolvate
    Acta Crystallogr., Sect E 2014, E70, o393. (DOI)
  • N. Koch, M. Mazik
    Synthesis of Tripodal and Hexapodal Pyrazole and Benzimidazole-Bearing Compounds
    Synthesis 2013, 45(24), 3341-3348. (DOI)
  • J. Lippe, M. Mazik
    Artificial Receptors Inspired by Crystal Structures of Complexes Formed between Acyclic Receptors and Monosaccharides: Design, Syntheses and Binding Properties
    J. Org. Chem. 2013, 78, 9013-9020. (DOI)
  • J.-R. Rosien, W. Seichter, M. Mazik
    Trimethoxybenzene- and trimethylbenzene-based compounds bearing imidazole, indole and pyrrole groups as recognition units: synthesis and evaluation of the binding properties towards carbohydrates
    Org. Biomol. Chem. 2013, 11, 6569-6579. (DOI)
  • J.-R. Rosien. W. Seichter, M. Mazik
    2,2',2''-[(2,4,6-Trimethoxybenzene-1,3,5-triyl)tris(methylene)]tris(isoindole-1,3-dione)
    Acta Crystallogr., Sect. E 2013, E69, o680. (DOI)
  • N. Koch, W. Seichter, M. Mazik
    1,3,5-Tris(bromomethyl)-2,4,6-trimethoxybenzene
    Acta Crystallogr., Sect. E 2013, E69, o679. (DOI)
  • C. Geffert, M. Kuschel, M. Mazik
    Molecular Recognition of N-Acetylneuraminic Acid by Acyclic Pyridinium- and Quinolinium-Based Receptors in Aqueous Media: Recognition through Combination of Cationic and Neutral Recognition Sites
    J. Org. Chem. 2013, 78 (2), 292-300. (DOI)
  • C. Sonnenberg, A. Hartmann, M. Mazik
    Molecular recognition of carbohydrates: Evaluation of the binding properties of pyrazole-based receptors and their comparison with imidazole- and indole-based systems
    Nat. Prod. Commun. 2012, 7, 321-326.
  • M. Mazik
    Recent developments in the molecular recognition of carbohydrates by artificial receptors
    RSC Advances 2012, 2, 2630-2642. (DOI)
  • M. Mazik, C. Geffert
    8-Hydroxyquinoline as a Building Block for Artificial Receptors: Binding Preferences in the Recognition of Glycopyranosides
    Org. Biomol. Chem. 2011, 9, 2319-2326. (DOI)
  • M. Mazik, C. Sonnenberg
    Isopropylamino and isobutylamino groups as recognition sites for carbohydrates: acyclic receptors with enhanced binding affinity towards ß-galactosides
    J. Org. Chem. 2010, 75, 6416-6423. (DOI)
  • M. Mazik, A. Hartmann
    Recognition properties of receptors consisting of imidazole and indole recognition units toward carbohydrates
    Beilstein J. Org. Chem. 2010, 6, No. 9. (DOI)
  • M. Mazik, A. Buthe
    C-H···Br, C-Br···Br and C-Br···π interactions in the crystal structures of mesitylene- and dimesitylmethane-derived compounds bearing bromomethyl units
    Tetrahedron, 2010, 66, 385-389. (DOI)
  • M. Mazik, A. Hartmann, P. G. Jones
    Hydrogen and halogen bonding in the crystal structure of a 1,3,5-substituted 2,4,6-triethylbenzene consisting of three phenanthroline units
    Eur. J. Org. Chem. 2010, 3, 458-463. (DOI)
  • M. Mazik, A. Hartmann, P. G. Jones
    Highly effective recognition of carbohydrates by phenanthroline-based receptors: a- vs. ß-anomer binding preference
    Chem. Eur. J. 2009, 15, 9147-9159. (DOI)
  • M. Mazik, A. Buthe
    Recognition properties of receptors based on dimesitylmethane-derived core: Di- vs. Monosaccharide Preference
    Org. Biomol. Chem. 2009, 7, 2063-2071. (DOI)
  • M. Mazik
    Molecular recognition of carbohydrates by acyclic receptors employing noncovalent interactions
    Chem. Soc. Rev. 2009, 38, 935-956. (DOI)
  • M. Mazik, A. Hartmann
    Phenanthrolin unit as building block for carbohydrate receptors
    J. Org. Chem. 2008, 73, 7444-7450. (DOI)
  • M. Mazik, A. Buthe
    Highly effective receptors showing Di- vs. Monosaccharide Preference
    Org. Biomol. Chem. 2008, 6, 1558-1568. (DOI)
  • M. Mazik
    Design of Lectin Mimetics
    ChemBioChem. 2008, 9, 1015-1017. (DOI)
  • M. Mazik, M. Kuschel
    Amide, Amino, Hydroxy and Aminopyridine Groups as Building Blocks for Carbohydrate Receptors
    Eur. J. Org. Chem. 2008, 9, 1517-1526. (DOI)
  • M. Mazik, M. Kuschel
    Highly Effective Acyclic Carbohydrate Receptors Consisting of Aminopyridine, Imidazole and Indole Recognition Units
    Chem. Eur. J. 2008, 14, 2405-2419. (DOI)
  • M. Mazik, A. Buthe
    Oxime-Based Receptors for Mono- and Disaccharides
    J. Org. Chem. 2007, 72, 8319-8326. (DOI)
  • M. Mazik, A. König
    Mimicking the binding motifs found in the crystal structures of protein-carbohydrate complexes: an aromatic analogue of serine or threonine side chain hydroxyl/main chain amide
    Eur. J. Org. Chem. 2007, 20, 3271-3276. (DOI)
  • M. Mazik, H. Cavga
    An acyclic aminonaphthyridine-based receptor for carbohydrate recognition: binding studies in competitive solvents
    Eur. J. Org. Chem. 2007, 22, 3633-3638. (DOI)
  • M. Mazik, H. Cavga
    Molecular Recognition of N-Acetylneuraminicacid  with acyclic benzimidazolium- and aminopyridine/guanidinium-based receptors
    J. Org. Chem. 2007, 73, 831-838. (DOI)
  • M. Mazik, A. König
    Recognition Properties of an Acyclic Biphenyl-Based Receptor toward Carbohydrates
    J. Org. Chem. 2006, 71, 7854-7857. (DOI)
  • M. Mazik, H. Cavga
    Carboxylate-Based Receptors for the Recognition of Carbohydrates in Organic and Aqueous Media
    J. Org. Chem. 2006, 71, 2957-2963. (DOI)
  • M. Mazik, M. Kuschel, W. Sicking
    Crown Ether as Building Blocks for Carbohydrate Receptors
    Org. Lett. 2006, 8, 855-858. (DOI)
  • M. Mazik, D. Bläser, R. Boese
    α, β-unsaturated ketoximes carrying a terminal pyridine or quinoline subunit as building blocks for supramolecular syntheses
    J. Org. Chem. 2005, 70, 9115-9122. (DOI)
  • M. Mazik, H. Cavga, P. G. Jones
    Molecular recognition of carbohydrates with artificial receptors. Mimicking the binding motifs found in the crystal structures of protein-carbohydrate complexes
    J. Am. Chem. Soc. 2005127, 9045-9052. (DOI)
  • U. Lottermoser, P. Rademacher, M. Mazik, K. Kowski
    Photoelectron spectra and electronic structures of substituted pyrimidines
    Eur. J. Org. Chem. 2005, 522-531. (DOI)
  • M. Mazik, W. Radunz, R. Boese
    Molecular recognition of carbohydrates with acyclic pyridine-based receptors
    J. Org. Chem. 2004, 69, 7448-7462. (DOI)
  • M. Mazik, W. Sicking
    Pyridine-based receptors with high affinity for monosaccharides. Influence of the degree of steric hindrance at pyridine nitrogen on the binding mode
    Tetrahedron Lett. 2004, 45, 3117-3121. (DOI)
  • W. Zielinski, A. Kudelko, W. Czardybon, M. Mazik
    Application of N-vinylimidoyl, N-arylimidoyl and hydrazonyl compounds in the synthesis of N-heterocycles
    Trends Heterocycl. Chem. 2003, 9, 69-82. 
  • M. Mazik, W. Radunz, W. Sicking
    High α/β-anomer selectivity in the molecular recognition of carbohydrates by artificial receptors
    Org. Lett. 2002, 4, 4579-4582. (DOI)
  • M. Mazik, W. Sicking
    Molecular recognition of carbohydrates by artificial receptors: Systematic study towards recognition motifs for carbohydrates
    Chem. Eur. J. 2001, 7, 664-670. (DOI)
  • M. Mazik, D. Bläser, R. Boese
    Intermolecular CH····N/CH····O hydrogen bonds in the crystal structures of α, β-unsaturated ketones carrying a terminal pyridine subunit
    Tetrahedron 2001, 57, 5791-5797. (DOI)
  • M. Mazik, H. Bandmann, W. Sicking
    Molecular recognition of carbohydrates by artificial polypyridine and polypyrimidine receptors
    Angew. Chem. 2000, 112, 562-565. (DOI)
    Angew. Chem. Int. Ed. Engl. 2000, 39, 551-554. (DOI)
  • M. Mazik, D. Bläser, R. Boese
    Programmed construction of discrete self-assembled cyclic aggregates
    Chem. Eur. J. 2000, 6, 2865-2873. (DOI)
  • M. Mazik, D. Bläser, R. Boese
    The potential of CH···N interactions in determining the crystal structures of novel 3,4-disubstituted-5-pyridinyl-isoxazoles
    Tetrahedron Lett. 2000, 41, 5827-5831. (DOI)
  • M. Mazik, D. Bläser, R. Boese
    Control of molecular self-assembly by hydrogen-bonding and aromatic interactions: Formation of discrete cyclic tetrameric aggregates
    Tetrahedron 1999, 55, 7835-7840. (DOI)
  • M. Mazik, D. Bläser, R. Boese
    New helical hydrogen-bonded assemblies forming channel-inclusion complexes
    Tetrahedron. Lett. 1999, 40, 4783-4786. (DOI)
  • M. Mazik, D. Bläser, R. Boese
    Hydrogen bonding motifs in the crystals of secondary diamides with 2-Amino-6-methyl- and 2,6-diaminopyridine subunits
    Tetrahedron 1999, 55, 12771-12782. (DOI)
  • M. Mazik, R. Boese, R. Sustmann
    Titanium(IV) chloride induced reaction of ketones and C-acylimines with dimethylcyanamide
    Liebigs. Ann. 1996, 1665-1671. (DOI)
  • S. Krompiec, M. Mazik, W. Zielinski, P. Wagner, M. Smolik
    Synthesis of 2-aza-1,3-dienes
    Pol. J. Chem. 1996, 70, 1223-1227.
  • M. Mazik, W. Zielinski
    Basicity of 4-aminopyrimidine and 2,4-diaminopyrimidine derivatives
    Monatsh. Chem. 1996, 127, 587-591. (DOI)
  • M. Mazik, W. Zielinski
    Synthesis of pyridinyl-4-pyrimidinamine derivatives
    Monatsh. Chem. 1996, 127, 1161-1165. (DOI)
  • M. Mazik, R. Boese, R. Sustmann
    Reaction of 1,2-diketones with dimethylcyanamide in the presence of titanium(IV)chloride
    Tetrahedron 1996, 52, 3939-3946. (DOI)
  • W. Zielinski, A. Kudelko, M. Mazik
    Electronic effects in isoquinoline system
    Polish J. Appl. Chem. 1995, 39, 33-38.
  • W. Zielinski, M. Mazik, A. Kudelko
    Imidic acid derivatives in the synthesis of 1,3-diazines
    Khim. Geterotsikl. Soedin. 1995, 1380-1382.
  • W. Zielinski, M. Mazik
    Syntheses of 2,4-diaminopyrimidines and 1-aminoisoquinolines in the reaction of allyl and benzyl ketones with cyanamide and N,N-dimethylcyanamide
    Heterocycles 1994, 38, 375-382. (DOI)
  • W. Zielinski, M. Mazik
    Synthesis of 4-aminoquinazoline derivatives
    Polish J. Chem. 1994, 68, 489-497.
  • W. Zielinski, M. Mazik
    A simple method for synthesis of 4-dimethylamino-2,6-dimethyl-5-phenylpyrimidines
    Heterocycles 1993, 36, 1521-1528. (DOI)
  • W. Zielinski, M. Mazik
    Reaction of N-styrylacetimidoyl chlorides with cyanamide
    Polish J. Chem. 1993, 67, 1099-1104.
  • W. Zielinski, M. Mazik
    Synthesis, tautomerisation and acylation of 1-phenylpropane-2-imines
    Polish J. Chem. 1992, 66, 661-668.
  • W. Zielinski, M. Mazik
    Studies on the reaction of N-vinylimidoyl compounds with acetylenicdienophiles
    Polish J. Chem. 1992, 66, 1113-1119.