All Stories

  1. On the antioxidant activity of eumelanin biopigments: a quantitative comparison between free radical scavenging and redox properties
  2. Stem cell-compatible eumelanin biointerface fabricated by chemically controlled solid state polymerization
  3. Supplementing π-systems: eumelanin and graphene-like integration towards highly conductive materials for the mammalian cell culture bio-interface
  4. Superior Photoprotective Motifs and Mechanisms in Eumelanins Uncovered
  5. Bioelectronics: In Situ Formation of Dendrites in Eumelanin Thin Films between Gold Electrodes (Adv. Funct. Mater. 45/2013)
  6. Neuroglobin Modification by Reactive Quinone Species
  7. Eumelanin: An Old Natural Pigment and a New Material for Organic Electronics – Chemical, Physical, and Structural Properties in Relation to Potential Applications
  8. Free Radical Coupling of o-Semiquinones Uncovered
  9. Melanins and melanogenesis: methods, standards, protocols
  10. In Situ Formation of Dendrites in Eumelanin Thin Films between Gold Electrodes
  11. Excited-State Proton-Transfer Processes of DHICA Resolved: From Sub-Picoseconds to Nanoseconds
  12. Towards the development of a novel bioinspired functional material: Synthesis and characterization of hybrid TiO2/DHICA-melanin nanoparticles
  13. Irreversible evolution of eumelanin redox states detected by an organic electrochemical transistor: en route to bioelectronics and biosensing
  14. Intermolecular π‐Electron Perturbations Generate Extrinsic Visible Contributions to Eumelanin Black Chromophore in Model Polymers with Interrupted Interring Conjugation
  15. Bottom-Up Approach to Eumelanin Photoprotection: Emission Dynamics in Parallel Sets of Water-Soluble 5,6-Dihydroxyindole-Based Model Systems
  16. Heparin conjugated silica nanoparticle synthesis
  17. Glycosylated Eumelanin Building Blocks by Thioglycosylation of 5,6‐Diacetoxyindole with an Expedient Selenium‐Based Dynamic‐Mixture Methodology
  18. Eumelanin Buildup on the Nanoscale: Aggregate Growth/Assembly and Visible Absorption Development in Biomimetic 5,6-Dihydroxyindole Polymerization.
  19. Photovoltaic properties of PSi impregnated with eumelanin
  20. Atropodiastereoselectivity in solid state BINOL synthesis: Leads from the estradiol platform
  21. Exploring the frontiers of synthetic eumelanin polymers by high‐resolution matrix‐assisted laser/desorption ionization mass spectrometry
  22. 5,6‐Dihydroxyindole Chemistry: Unexplored Opportunities Beyond Eumelanin
  23. Structure of Melanins
  24. π-Electron Manipulation of the 5,6-Dihydroxyindole/Quinone System by 3-Alkynylation: Mild Acid-Mediated Entry to (Cross)-Conjugated Scaffolds and Paradigms for Medium-Tunable Chromophores
  25. Functionality of epidermal melanin pigments: current knowledge on UV-dissipative mechanisms and research perspectives
  26. UV‐Dissipation Mechanisms in the Eumelanin Building Block DHICA
  27. Cyclic Structural Motifs in 5,6-Dihydroxyindole Polymerization Uncovered: Biomimetic Modular Buildup of a Unique Five-Membered Macrocycle
  28. Reaction of dihydrolipoic acid with juglone and related naphthoquinones: unmasking of a spirocyclic 1,3-dithiane intermediate en route to naphtho[1,4]dithiepines
  29. 5,6‐Dihydroxyindole Oxidation in Phosphate Buffer/Polyvinyl Alcohol: A New Model System for Studies of Visible Chromophore Development in Synthetic Eumelanin Polymers
  30. First synthetic entry to the trimer stage of 5,6-dihydroxyindole polymerization: ortho-alkynylaniline-based access to the missing 2,7′:2′,7′′-triindole
  31. Disentangling Eumelanin “Black Chromophore”: Visible Absorption Changes As Signatures of Oxidation State- and Aggregation-Dependent Dynamic Interactions in a Model Water-Soluble 5,6-Dihydroxyindole Polymer
  32. Ultrafast Excited State Dynamics of 5,6-Dihydroxyindole, A Key Eumelanin Building Block: Nonradiative Decay Mechanism
  33. Efficient Synthesis of 5,6-Dihydroxyindole Dimers, Key Eumelanin Building Blocks, by a Unified o-Ethynylaniline-Based Strategy for the Construction of 2-Linked Biindolyl Scaffolds
  34. ChemInform Abstract: Chemical and Structural Diversity in Eumelanins: Unexplored Bio‐Optoelectronic Materials
  35. Chemische und strukturelle Vielfalt der Eumelanine – ein kaum erforschtes optoelektronisches Biopolymer
  36. Chemical and Structural Diversity in Eumelanins: Unexplored Bio‐Optoelectronic Materials
  37. Lack of Visible Chromophore Development in the Pulse Radiolysis Oxidation of 5,6-Dihydroxyindole-2-carboxylic Acid Oligomers: DFT Investigation and Implications for Eumelanin Absorption Properties
  38. A novel fluoride-sensing scaffold by a peculiar acid-promoted trimerization of 5,6-dihydroxyindole
  39. Plant Catechols and Their S-Glutathionyl Conjugates as Antinitrosating Agents: Expedient Synthesis and Remarkable Potency of 5-S-Glutathionylpiceatannol
  40. ChemInform Abstract: Mild and Efficient Iodination of Aromatic and Heterocyclic Compounds with the NaClO2/NaI/HCl System.
  41. Mild and efficient iodination of aromatic and heterocyclic compounds with the NaClO2/NaI/HCl system
  42. Structural Effects on the Electronic Absorption Properties of 5,6‐Dihydroxyindole Oligomers: The Potential of an Integrated Experimental and DFT Approach to Model Eumelanin Optical Properties†
  43. 5,6-Dihydroxyindole Tetramers with “Anomalous” Interunit Bonding Patterns by Oxidative Coupling of 5,5‘,6,6‘-Tetrahydroxy-2,7‘-biindolyl:  Emerging Complexities on the Way toward an Improved Model of Eumelanin Buildup
  44. The First Entry to 5,6‐Dihydroxy‐3‐mercaptoindole, 5‐Hydroxy‐3‐mercaptoindole and Their 2‐Carbomethoxy Derivatives by a Mild Thiocyanation/Reduction Methodology.
  45. The first entry to 5,6-dihydroxy-3-mercaptoindole, 5-hydroxy-3-mercaptoindole and their 2-carbomethoxy derivatives by a mild thiocyanation/reduction methodology
  46. The First 5,6-Dihydroxyindole Tetramer by Oxidation of 5,5‘,6,6‘-Tetrahydroxy- 2,4‘-biindolyl and an Unexpected Issue of Positional Reactivity en Route to Eumelanin-Related Polymers
  47. Chemical, Pulse Radiolysis and Density Functional Studies of a New, Labile 5,6-Indolequinone and Its Semiquinone
  48. Preparation and Oxidation Chemistry of the Catechol Estrogens: Relevance to Estrogen-Related Carcinogenesis and Potential for Drug Design
  49. Short-Lived Quinonoid Species from 5,6-Dihydroxyindole Dimers en Route to Eumelanin Polymers:  Integrated Chemical, Pulse Radiolytic, and Quantum Mechanical Investigation
  50. Practical one-pot conversion of 17β-estradiol to 10β-hydroxy- (p-quinol) and 10β-chloro-17β-hydroxyestra-1,4-dien-3-one
  51. The role of residue Thr249 in modulating the catalytic efficiency and substrate specificity of catechol‐2,3‐dioxygenase from Pseudomonas stutzeri OX1
  52. Acid-Promoted Reaction of the Stilbene Antioxidant Resveratrol with Nitrite Ions:  Mild Phenolic Oxidation at the 4‘-Hydroxystiryl Sector Triggering Nitration, Dimerization, and Aldehyde-Forming Routes
  53. Oxidative chemistry of the natural antioxidant hydroxytyrosol: hydrogen peroxide-dependent hydroxylation and hydroxyquinone/o-quinone coupling pathways
  54. 5,6‐Dihydroxyindoles and Indole‐5,6‐diones
  55. An Expedient One‐Pot Entry Catecholestrogens and Other Catechol Compounds via IBX‐Mediated Phenolic Oxygenation.
  56. Tyrosinase-Catalyzed Oxidation of 17β-Estradiol:  Structure Elucidation of the Products Formed beyond Catechol Estrogen Quinones
  57. An expedient one-pot entry to catecholestrogens and other catechol compounds via IBX-mediated phenolic oxygenation
  58. New insight into the oxidative chemistry of noradrenaline: competitive o-quinone cyclisation and chain fission routes leading to an unusual 4-[bis-(1H-5,6-dihydroxyindol-2-yl)methyl]-1,2-dihydroxybenzene derivative
  59. Regioselective Phenol or Carbinol Glycosidation of 17β-Estradiol and Derivatives Thereof
  60. 5,6-Dihydroxyindoles and Indole-5,6-diones
  61. Oxidative Coupling of 17β-Estradiol:  Inventory of Oligomer Products and Configuration Assignment of Atropoisomeric C4-Linked Biphenyl-Type Dimers and Trimers
  62. 17β-Estradiol nitration by peroxidase/H2O2/NO2−: a chemical assessment
  63. Oxidative chemistry of hydroxytyrosol: isolation and characterisation of novel methanooxocinobenzodioxinone derivatives
  64. Synthesis of optically active tetrameric melanin intermediates by oxidation of the melanogenic precursor 5,6-dihydroxyindole-2-carboxylic acid under biomimetic conditions
  65. Formation of novel tetrahydroisoquinoline retinoids by Pictet–Spengler reaction of dopamine and retinaldehyde under conditions of relevance to biological environments
  66. Atropoisomeric melanin intermediates by oxidation of the melanogenic precursor 5,6-dihydroxyindole-2-carboxylic acid under biomimetic conditions
  67. Generation of Neurotoxins by New Reaction Pathways of Dopamine under Oxidative Stress Conditions: Contributing Etiopathological Factors in Parkinson’s Disease
  68. New Reaction Pathways of Dopamine under Oxidative Stress Conditions:  Nonenzymatic Iron-Assisted Conversion to Norepinephrine and the Neurotoxins 6-Hydroxydopamine and 6,7-Dihydroxytetrahydroisoquinoline
  69. 6,7-Dihydroxy-1,2,3,4-tetrahydroisoquinoline formation by iron mediated dopamine oxidation: a novel route to endogenous neurotoxins under oxidative stress conditions
  70. New directions in Parkinson’s research and treatment
  71. Iron-Mediated Generation of the Neurotoxin 6-Hydroxydopamine Quinone by Reaction of Fatty Acid Hydroperoxides with Dopamine:  A Possible Contributory Mechanism for Neuronal Degeneration in Parkinson's Disease
  72. An integrated approach to the structure of Sepia melanin. Evidence for a high proportion of degraded 5,6-dihydroxyindole-2-carboxylic acid units in the pigment backbone
  73. Identification of Partially Degraded Oligomers of 5,6-Dihydroxyindole-2-carboxylic Acid inSepia Melanin by Matrix-assisted Laser Desorption/Ionization Mass Spectrometry
  74. Mass Spectrometric Behavior of 5-S-Cysteinyldopa and Structurally Related Phenolic Compounds. Fragmentation Susceptibility of the Alkylthioether Bond Under Electron Impact and Fast Atom Bombardment Conditions
  75. Mass Spectrometric Behavior of 5-S-Cysteinyldopa and Structurally Related Phenolic Compounds. Fragmentation Susceptibility of the Alkylthioether Bond Under Electron Impact and Fast Atom Bombardment Conditions
  76. The first characterisation of a transient 5,6-indolequinone
  77. New pyrrole acids by oxidative degradation of eumelanins with hydrogen peroxide. Further hints to the mechanism of pigment breakdown
  78. Oxidative polymerisation of 5,6-dihydroxyindole-2-carboxylic acid to melanin: A new insight
  79. Structural Analysis of Synthetic Melanins from 5,6-Dihydroxyindole by Matrix‐assisted Laser Desorption/Ionization Mass Spectrometry
  80. Structural Analysis of Synthetic Melanins from 5,6-Dihydroxyindole by Matrix-assisted Laser Desorption/Ionization Mass Spectrometry
  81. A Reassessment of the Structure of 5,6-Dihydroxyindole-2-carboxylic Acid Melanins by Matrix‐assisted Laser Desorption/Ionization Mass Spectrometry
  82. A Reassessment of the Structure of 5,6-Dihydroxyindole-2-carboxylic Acid Melanins by Matrix-assisted Laser Desorption/Ionization Mass Spectrometry
  83. Oxidative degradation of melanins to pyrrole acids: A model study
  84. Generation of the Neurotoxin 6-Hydroxydopamine by Peroxidase/H2O2 Oxidation of Dopamine
  85. The origin of pyrrole-2,3,5-tricarboxylic acid by oxidative degradation of eumelanins