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Synthesis and in vitro carbonic anhydrases and acetylcholinesterase inhibitory activities of novel imidazolinone‐based benzenesulfonamides

Archiv der Pharmazie, 2020
New imidazolinone‐based benzenesulfonamides 3a–e and 4a–e were synthesized in three steps and their chemical structures were confirmed by 1H NMR (nuclear magnetic resonance), 13C NMR, and high‐resolution mass spectrometry.
M. Tuğrak   +4 more
semanticscholar   +1 more source

A Novel Imidazolinone Derivative with 5‐Arylidene and 2‐Substituted Mercapto Group as Potent Anti‐Hepatitis C Virus Compound

Chemistry and Biodiversity, 2021
Here six novel imidazolinone derivatives have been synthesized and the compound 4b containing 5‐para‐methoxy‐phenylidene and 2‐thioalkylation terminal substitution with 3’‐cyano‐2’,6’‐dimethylphenyl showed the best anti‐HCV activity and the lowest ...
Ying Kong   +5 more
semanticscholar   +1 more source

Synthesis of 2-imidazolinones

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1985
2-Imidazolinones were synthesized by heating α-bromoketones with urea in ethyleneglycol in the presence of potassium carbonate.
S. I. Zav'yalov   +2 more
openaire   +1 more source

Computational study of organic small molecules based on imidazolinone for photovoltaic applications

, 2020
Organic photovoltaic cells have received significant interest due to the low-cost manufacturing and compatibility to deposit on flexible substrate. However, this technology suffers from certain problems including lowest solar spectrum absorption by ...
A. Aboulouard   +2 more
semanticscholar   +1 more source

Copper(II) complexes of imidazolinone herbicides

Inorganica Chimica Acta, 1997
Abstract The copper(II) complexes formed by the imidazolinone herbicide Imazapyr or (±)-2-4-isopropyl-(4-methyl-5-oxo-2-imidazolin-2-yl)-nicotinic acid (H 2 imz) are described. The compounds isolated in the solid state confirm that Imazapyr is a versatile bipy-like ligand able to chelate the metal ion through two different donor sets.
Liliana Strinna Erre   +4 more
openaire   +3 more sources

The asymmetric reduction of imidazolinones with trichlorosilane

Chemical Communications, 2017
The asymmetric reduction of imidazolinones with trichlorosilane is described, catalyzed through a chiral bispyrrolidine organocatalyst.
Christian Wagner   +2 more
openaire   +2 more sources

Efficacy of imidazolinone herbicides applied to imidazolinone-resistant maize and their carryover effect on rotational crops

Crop Protection, 2005
Abstract A field study was performed in imidazolinone-resistant maize in order to evaluate the effectiveness and carryover effect on rotational crops of two formulated mixtures of imidazolinone herbicides: imazapyr plus imazapic and imazapyr plus imazethapyr.
Alister, C, Kogan, M
openaire   +2 more sources

Synthesis of 4,5-disubstituted imidazolinones-2

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1989
1. 4-Methyl-5-(α-oxo-Β-bromo-e-ethoxycarbonylpentyl)imidazolinone-2 reacts with diethylamine with migration of the electrophilic reaction center to give 4-diethylaminomethyl-5-(α-oxo-e-ethoxycarbonylpentyl)imidazolinone-2. 2. Sulfur-containing nucleophilic reagents and potassium benzoate enter into a nucleophilic substitution reaction ...
S. I. Zav'yalov   +2 more
openaire   +1 more source

Syntheses of ?-functionally substituted 2-imidazolinones

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1979
1. The Mannich and Vilsmeier reactions with 4(5)-methyl-2-imidazolinone proceed with involvement of the C5(4) carbon atom. 2. The reaction of 4(5)-methyl-5(4)-piperidinomethyl-2-imidazolinone with a mixture of thioacetic acid and acetic anhydride gives 1-acetyl-4-acetylmercaptomethyl-5-methyl-2-imidazolinone. 3.
S. I. Zav'yalov   +2 more
openaire   +1 more source

Abiotic degradation (photodegradation and hydrolysis) of imidazolinone herbicides

Journal of Environmental Science and Health, Part B, 2008
The abiotic degradation of the imidazolinone herbicides imazapyr, imazethapyr and imazaquin was investigated under controlled conditions. Hydrolysis, where it occurred, and photodegradation both followed first-order kinetics for all herbicides.
Ramezani, M.   +4 more
openaire   +3 more sources

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