ΕΘΝΙΚΟ ΚΑΙ ΚΑΠΟΔΙΣΤΡΙΑΚΟ ΠΑΝΕΠΙΣΤΗΜΙΟ ΑΘΗΝΩΝ ΣΧΟΛΗ ΘΕΤΙΚΩΝ ΕΠΙΣΤΗΜΩΝ ΤΜΗΜΑ ΧΗΜΕΙΑΣ

Chapter 18 Electrochemistry

CROMATOGRAFÍA

Bromolysis and Iodolysis of α,β-Epoxycarboxylic Acids in Water Catalyzed by Indium Halides

[Au 2 (phen 2Me ) 2 (μ - O) 2 ](PF 6 ) 2 , a Novel Dinuclear Gold(III) Complex Showing Excellent Antiproliferative Properties

Amberlite IRA900N 3 as a New Catalyst for the Azidation of α,β-Unsaturated Ketones under Solvent-Free Conditions

Possible role of the α7 nicotinic receptors in mediating nicotine’s effect on developing lung – implications in unexplained human perinatal death

Wiley Encyclopedia of Composites || Angle Ply Laminates

Mo1162 Inflammation Increases Notch1 Activity in Colorectal Cancer Cells and Is Counteracted by Eicosapentaenoic Acid-Free Fatty Acid

Lysine acetylation in the lumen of the ER: A novel and essential function under the control of the UPR

Identification and Quantification of α S1 , α S2 , β, and κ-Caseins in Water Buffalo Milk by Reverse Phase-High Performance Liquid Chromatography and Mass Spectrometry

A Tale of Cosmic Rays Narrated in γ Rays by Fermi

Synthesis of α-Galactosyl Ceramide (KRN7000) and Analogues Thereof via a Common Precursor and Their Preliminary Biological Assessment

Biophysical groundwork as a hinge to unravel the biology of α-synuclein aggregation and toxicity

Optimized Use of a 50 μm Internal Diameter Secondary Column in a Comprehensive Two-Dimensional Gas Chromatography System

Parametrization of an Empirical Correction Term to Density Functional Theory for an Accurate Description of π-Stacking Interactions in Nucleic Acids

Azidolysis of α,β-Epoxycarboxylic Acids. A Water-Promoted Process Efficiently Catalyzed by Indium Trichloride at pH 4.0

Azidolysis of α,β-Epoxycarboxylic Acids. A Water-Promoted Process Efficiently Catalyzed by Indium Trichloride at pH 4.0

Synthesis and Pharmacological Evaluation of a Selected Library of New Potential Anti-inflammatory Agents Bearing the γ-Hydroxybutenolide Scaffold:  a New Class of Inhibitors of Prostanoid

γ-Valerolactone as a Renewable Dipolar Aprotic Solvent Deriving from Biomass Degradation for the Hiyama Reaction