Results 31 to 40 of about 61,390 (300)

Catalysis by tertiary chalcogenonium salts

open access: yesTetrahedron Chem, 2023
The synthetic utility of onium salts is widely recognized in organic chemistry. Among the wide variety of onium salt compounds, quaternary ammonium and phosphonium salts are known as representative organocatalysts.
Ken Okuno   +2 more
doaj   +1 more source

Synthesis, Purification and Characterization of Polymerizable Multifunctional Quaternary Ammonium Compounds

open access: yesMolecules, 2019
Methacrylate analogs of quaternary ammonium salts functionalized with carboxylic (AMadh1 68.8% yield, AMadh2 53.2% yield) and methoxysilane (AMsil1 94.8% yield, AMsil2 36.0% yield) groups were synthesized via Menschutkin reaction.
Ugochukwu C. Okeke   +2 more
doaj   +1 more source

Tetraalkylammonium and phosphonium salt for asphaltene dispersion; experimental studies on interaction mechanisms

open access: yesEgyptian Journal of Petroleum, 2022
Asphaltenes deposition is one of the most severe problems in the petroleum industry, imposing high costs on oil producer companies. The use of chemical dispersants reduces the risk of asphaltene deposition.
Shirin Baghersaei   +3 more
doaj   +1 more source

Metal organic ionic framework based on the ionic metal complex and organic moiety as counter ion: A review

open access: yesHybrid Advances, 2022
Metal organic ionic frameworks (MOIFs) or inorgano-organic salts (IOSs) are the product of an ionic interaction between metal ionic complex and opposite organic ion in water, through ion exchange mechanism.
Rakesh Kumar Ameta
doaj   +1 more source

Curare-like Action of Polymethylene bis-Quaternary Ammonium Salts [PDF]

open access: yesNature, 1948
H.R. (Raymond) Ing was a chemist who developed a unique understanding of pharmacology, which arose from working on alkaloid chemistry. To the chemist he is Ing of the Ing and Manske reaction (for the preparation of primary amines) and responsible for working out the structure of the alkaloid cytisine.
R B, BARLOW, H R, ING
openaire   +5 more sources

Synthesis of Quinacridone Derivatives and Their Application as High Performance Levelers in Electroplating

open access: yesElectrochemistry
A series of quaternary ammonium salts base on quinacridone aromatic ring were synthesized using 2,9-quinacridone as the parent material, and their leveling performance were evaluated using constant-current chronoamperometry addition curves. Additionally,
Peikun ZOU   +5 more
doaj   +1 more source

Synthesis, characterization, and bioactivity of rosin quaternary ammonium salt derivatives [PDF]

open access: yesBioResources, 2013
Two series of rosin quaternary ammonium salts (QAS) were synthesized using the same path. The structure of the target products was characterized by HPLC, MS, IR, and 1HNMR, and the bioactivity was determined by filter paper method using Trametes ...
Tao Liang   +3 more
doaj  

A Remarkably Efficient Phase-Transfer Catalyzed Amination of α-Bromo-α, β-Unsaturated Ketones in Water

open access: yesHeteroatom Chemistry, 2021
Tandem conjugate addition–alkylation reaction of various amines with α-bromo-α, β-unsaturated ketones resulted in near-quantitative conversions into the corresponding aziridines when the reaction was carried out in the presence of 10 mol% of phase ...
Alemayehu Mekonnen, Alemu Tesfaye
doaj   +1 more source

Antifungal activity of gemini quaternary ammonium salts

open access: yesMicrobiological Research, 2013
A series of gemini quaternary ammonium chlorides and bromides with various alkyl chain and spacer lengths was synthesized. The most active compounds against fungi were chlorides with 10 carbon atoms within the hydrophobic chain. Among these compounds were few with no hemolytic activity at minimal inhibitory concentrations.
Obłąk, Ewa   +3 more
openaire   +2 more sources

Targeting TNBC: core–shell polycationic polyurea dendrimers with inherent anticancer activity

open access: yesFEBS Open Bio, EarlyView.
Core–shell polycationic PURE dendrimers were tested in TNBC‐derived tumor models. Both formulations selectively targeted TNBC and effectively reduced tumor volume. PUREG4‐OEI48 suppressed tumor growth without detectable toxicity, whereas PUREG4‐OCEI24, despite showing efficacy, induced hepatic toxicity.
Adriana Cruz   +9 more
wiley   +1 more source

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