Results 1 to 10 of about 1,849 (201)
The inhibitory effect of nine phenylcarbamates with various substituents was studied. For this purpose, electrochemical sensors were applied under two different conditions: if an enzyme was present in the solution or if the enzyme was immobilized onto ...
Katarina Vorčáková +2 more
exaly +3 more sources
Molecular Dynamics Simulations of Amylose- and Cellulose-Based Selectors and Related Enantioseparations in Liquid Phase Chromatography [PDF]
In the last few decades, theoretical and technical advancements in computer facilities and computational techniques have made molecular modeling a useful tool in liquid-phase enantioseparation science for exploring enantioselective recognition mechanisms
Roberto Dallocchio +3 more
doaj +2 more sources
Several commercial vineyards, located in Piedmont (Northern Italy), were monitored in order to evaluate the sensitivity of Botrytis cinerea Pers., the causal agent of grey mould, to five classes of botryticides: benzimidazoles, dicarboximides ...
Angelo Garibaldi +3 more
doaj +3 more sources
Stable bitriptyceneazulene quinones have been prepared by Lewis acid induced coupling of triptyceneazulene quinones. Resolution of the enantiomers succeeded by high performance liquid chromatography (HPLC) on phenylcarbamates of cellulose.
Jörg Daub +3 more
doaj +3 more sources
Flower Induction in Seedlings of Asparagus officinalis L. by N-Phenylcarbamates
A series of N-phenylcarbamates induced flowers in one-month-old seedlings of Asparagus officinalis L. Ninety to 100% of the plants flowered when the seeds were germinated in the presence of the most potent members of this class.
Hajime Iwamura, Toshio Fujita
exaly +2 more sources
In the title compound, C13H11NO2, the aromatic rings are oriented at a dihedral angle of 42.52 (12)°. The crystal structure is stabilized by intermolecular N—H...O hydrogen bonds, which form infinite one-dimensional polymeric chains extending along theaaxis. C—H...π interactions between the aromatic rings are also present.
Durre Shahwar +4 more
openaire +3 more sources
Metabolism of ‘Propham’ (Isopropyl N-phenylcarbamate) in the Rat [PDF]
SEVERAL N-phenylcarbamates are currently used as selective pre and postemergent herbicides to control weeds in agronomic crops. Much is known of the fate of the N-phenylcarbamates in soils where micro-organisms play an important part in their decomposition1,2, and their metabolism has also been studied in plants3–5.
G M, Holder, A J, Ryan
openaire +2 more sources
Liquid-crystalline behavior of phenylcarbamate derivatives of cellulose in vinyl monomer solvents was investigated, and then calcium carbonate (CaCO3) mineralization was conducted in colored films wherein a cholesteric structure of the cellulosic ...
Kazuki Sugimura +3 more
semanticscholar +1 more source
Dibasic Derivatives of Phenylcarbamic Acid against Mycobacterial Strains: Old Drugs and New Tricks?
In order to provide a more detailed view on the structure–antimycobacterial activity relationship (SAR) of phenylcarbamic acid derivatives containing two centers of protonation, 1-[2-[({[2-/3-(alkoxy)phenyl]amino}carbonyl)oxy]-3-(dipropylammonio)propyl ...
Ivan Malík +12 more
doaj +1 more source
Introduction: Desmedipham + phenmedipham + ethofumesate, phenylcarbamates + benzofuranyl alkanesulfonate herbicides, is widely used for post-emergence broad-leaved weed control in sugar beet.
A.A. Chitband +3 more
doaj +1 more source

