Results 171 to 180 of about 41,455 (313)

The Dihydroindeno[2,1‐c]fluorene Core: from Syntheses to Properties and Potential Applications

open access: yesEuropean Journal of Organic Chemistry, Accepted Article.
In the last decade, substances possessing the dihydroindeno[2,1‐c]fluorene scaffold showed interesting photo‐physical properties and other potential applications in electronics. The afore‐mentioned compounds belong to the family of five regioisomeric dihydroindenofluorenes, but unlike other ones, they possess angular or, in the case of higher congeners,
Timothée Cadart, Martin Kotora
wiley   +1 more source

Hydrogen peroxide ‐ responsive aminoferrocene prodrugs

open access: yesEuropean Journal of Organic Chemistry, Accepted Article.
Aminoferrocene (AF)‐based prodrugs are activated in cancer cells through reactions with H₂O₂ and other reactive oxygen species (ROS), generating electron‐rich AF’s. These, in turn, induce the production of highly toxic O2·‐ and HO·, leading to cancer cell death.
Marlies Körber   +3 more
wiley   +1 more source

COQ4 is required for the oxidative decarboxylation of the C1 carbon of coenzyme Q in eukaryotic cells. [PDF]

open access: yesMol Cell
Pelosi L   +23 more
europepmc   +1 more source

Identifying the True Catalyst: A Mn(II) Salt versus Mn(II) Complexes in Epoxidation with m‐Chloroperbenzoic Acid

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
During the investigation of the reactivity of three Mn complexes, Mn(ClO4)2 shows higher reactivity toward styrene epoxidation, indicating that ligand coordination inhibits the reactivity of the manganese center. Raman spectroscopy provides mechanistic insight: monitoring alkene epoxidation and consumption of the oxidant over time, the true nature of ...
Milica Savić   +7 more
wiley   +1 more source

Cross‐Coupling Reactions in Aqueous Micellar Media

open access: yesEuropean Journal of Organic Chemistry, Accepted Article.
Thanks to their ability to efficiently and reliably construct carbon‐carbon and carbon‐heteroatom bonds, cross‐coupling reactions remain at the forefront of chemical research in both academic and industrial settings. However, the growing emphasis on sustainability has exposed the shortcomings of cross‐coupling chemistry in several areas, including the ...
Alexander Uner, Liam Thomas Ball
wiley   +1 more source

Photoredox Decarboxylative 3‐Fluoroallylation of α‐Amino Acids

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
An efficient, photocatalytic method for the decarboxylative 3‐fluoroallylation of α‐amino acids has been developed to produce fluorinated homoallylamines. A broad reaction scope is reported, including the use of dipeptides and different protecting groups on nitrogen.
Taylor Semeniuk   +5 more
wiley   +1 more source

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