Johann Bosson
0000-0002-4117-5638
Universite de Geneve
21 papers found
Refreshing results…
Merging polyacenes and cationic helicenes: from weak to intense chiroptical properties in the far red region
Stereochemical significance of O to N atom interchanges within cationic helicenes: experimental and computational evidence of near racemization to remarkable enantiospecificity
Ion Transfer Voltammetry in Polyurethane Thin Films Based on Functionalised Cationic [6]Helicenes for Carbonate Detection
Specific labeling of mitochondria of Chlamydomonas with cationic helicene fluorophores
Ion Transfer Voltammetry at Thin Films Based on Functionalized Cationic [6]Helicenes
Enantiospecific Elongation of Cationic Helicenes by Electrophilic Functionalization at Terminal Ends
Efficient Annihilation Electrochemiluminescence of Cationic Helicene Luminophores
Bright Electrochemiluminescence Tunable in the Near-Infrared of Chiral Cationic Helicene Chromophores
Cover Picture: Physicochemical and Electronic Properties of Cationic [6]Helicenes: from Chemical and Electrochemical Stabilities to Far-Red (Polarized) Luminescence (Chem. Eur. J. 51/2016)
High-Performance Liquid Chromatographic Resolution of Neutral and Cationic Hetero[6]Helicenes
Physicochemical and Electronic Properties of Cationic [6]Helicenes: from Chemical and Electrochemical Stabilities to Far-Red (Polarized) Luminescence
Electrogenerated Chemiluminescence of Cationic Triangulene Dyes: Crucial Influence of the Core Heteroatoms
Cationic triangulenes and helicenes: synthesis, chemical stability, optical properties and extended applications of these unusual dyes
Modular Synthesis, Orthogonal Post-Functionalization, Absorption, and Chiroptical Properties of Cationic [6]Helicenes
Development of Versatile and Silver-Free Protocols for Gold(I) Catalysis
Mechanism of Racemization of Chiral Alcohols Mediated by 16-Electron Ruthenium Complexes
N-Heterocyclic Carbene−Ruthenium Complexes for the Racemization of Chiral Alcohols
Au/Ag-Cocatalyzed Aldoximes to Amides Rearrangement under Solvent- and Acid-Free Conditions
Tetrahydrocyclopenta[c]acridine derivatives as kinase inhibitors and their therapeutic use
Acridine and Acridone Derivatives, Anticancer Properties and Synthetic Methods: Where Are We Now?
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