Results 1 to 10 of about 4,033 (225)

Tuning the electronic states of Pd(II) defect-engineered metal-organic framework catalysts for efficient conversion of isocyanides. [PDF]

open access: yesCommun Chem
Recently, defective sites in MOFs have become an important tool for tuning the catalytic performance of MOFs. Herein, we report a heterogeneous catalyst “Pd-UiO-67(N)x” by utilizing the active site of defective MOF to modulate the electronic state of Pd,
Su S, Cao Y, Ren Y, Jiang H, Wu W.
europepmc   +2 more sources

Selective alkylation of aminophenols [PDF]

open access: yesArkivoc, 2010
Oor N-Alkylated derivatives of aminophenols are important synthetic intermediates in organic synthesis. A series of aminophenols were selectively alkylated on their hydroxyl group in good yields via benzaldehyde protection of the amino group, subsequent alkylation, and hydrolysis; or on their amino group via imination and following reduction.
Jiaxi Xu, Renchao Wang
openaire   +3 more sources

General Synthesis of 2-Substituted Benzoxazoles Based on Tf<sub>2</sub>O-Promoted Electrophilic Activation of Tertiary Amides. [PDF]

open access: yesMolecules
We report a method for the synthesis of 2-substituted benzoxazoles from tertiary amides and 2-aminophenols in the presence of triflic anhydride (Tf2O) and 2-Fluoropyridine (2-F-Pyr).
Li H, Wang X, Zhao F, Wang L, Fu S.
europepmc   +2 more sources

Recent Progress on Covalent Organic Frameworks Supporting Metal Nanoparticles as Promising Materials for Nitrophenol Reduction. [PDF]

open access: yesNanomaterials (Basel)
With the utilization of nitrophenols in manufacturing various materials and the expansion of industry, nitrophenols have emerged as water pollutants that pose significant risks to both humans and the environment.
Dinari M   +5 more
europepmc   +2 more sources

Straightforward Access to Pentafluorosulfanylated Phenols and Aminophenols via [4 + 2] Diels-Alder Cycloaddition Reaction. [PDF]

open access: yesACS Org Inorg Au
Abd El Sater M   +5 more
europepmc   +2 more sources

Towards Efficient Catalysts via Biomimetic Chemistry for Diphenols and Aminophenols Aerobic Oxidation [PDF]

open access: yesIranian Journal of Chemistry & Chemical Engineering, 2023
Biomimetic chemistry is a new environment-friendly approach that is inspired by biological processes, to produce new catalysts, and to develop ‘green’ synthetic routes to chemical catalysts based on the benefits of biological systems, aimed to find ...
Abdeslam Mouadili   +2 more
doaj   +1 more source

An Optimised Method to Synthesise N5O2 Aminophenols

open access: yesChemistry Proceedings, 2023
Aminophenol compounds are usually employed in coordination chemistry due to their versatility to form metal complexes. Heptadentate N5O2 aminophenol ligands can lead to the formation of lanthanoid complexes with pentagonal bypiramidal (pbp) geometry ...
Paula Oreiro-Martínez   +3 more
doaj   +1 more source

Reactivity of aminophenols in forming nitrogen-containing brown carbon from iron-catalyzed reactions

open access: yesCommunications Chemistry, 2022
Iron is the most abundant redox active transition metal in mineral dust, but its role in nitrogen-containing organic carbon formation remains largely unexplored. Here, the authors show that Fe(III) catalyzes the dark oxidative oligomerization of o- and p-
Hind A. Al-Abadleh   +7 more
doaj   +1 more source

Protecting-group-free enantioselective tandem allylic substitution of o-phenylenediamines and o-aminophenols

open access: yesGreen Synthesis and Catalysis, 2022
A protecting-group-free enantioselective tandem allylic substitution of o-phenylenediamines and o-aminophenols is realized for the first time with a Pd-WingPhos catalyst, providing expedient access to a series of chiral vinyl-substituted heterocycles in ...
Xuehua Kang   +5 more
doaj   +1 more source

2-aminophenols containing electron-withdrawing groups from N-aryl hydroxylamines [PDF]

open access: yes, 2010
Reaction of substituted N-aryl hydroxylamines with methanesulfonyl chloride, p-toluenesulfonyl chloride, or trifluoromethanesulfonic anhydride under basic conditions leads to the rearranged 2-aminophenols (45-94%).
Cooper, Anthony W. J.   +3 more
core   +1 more source

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