Results 21 to 30 of about 48,307 (173)

2-(4-Methylbenzenesulfonamido)-2-phenylacetic acid

open access: yesActa Crystallographica Section E, 2009
In the title compound, C15H15NO4S, the dihedral angle between the phenyl and benzene rings is 46.0 (3)° and a weak intramolecular N—H...O interaction is present.
Irfana Mariam   +4 more
doaj   +1 more source

Antifungal Activity Evaluation of the Constituents of Haliclona baeri and Haliclona cymaeformis, Collected from the Gulf of Thailand

open access: yesMarine Drugs, 2007
A new compound maleimide-5-oxime was isolated, together with 3,4- dihydroxybenzoic acid, tetillapyrone, from the ethyl acetate extract of the marine sponge Haliclona baeri while tetillapyrone, nortetillapyrone, p-hydroxybenzaldehyde and phenylacetic acid
Anake Kijjoa   +7 more
doaj   +1 more source

2-(4-Bromobenzenesulfonamido)-2-phenylacetic acid monohydrate

open access: yesActa Crystallographica Section E, 2009
In the title compound, C14H12BrNO4S·H2O, the phenyl and benzene rings are inclined at a dihedral angle of 39.5 (5)°. The crystal packing is stabilized by N—H...O, C—H...O and O—H...O hydrogen ...
Muhammad Nadeem Arshad   +3 more
doaj   +1 more source

Crystallographic and spectroscopic characterization of (R)-O-acetylmandelic acid

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2016
The title compound [systematic name: (R)-(−)-2-acetoxy-2-phenylacetic acid], C10H10O4, is a resolved chiral ester derivative of mandelic acid. The compound contains an acetate group and a carboxylic acid group, which engage in intermolecular hydrogen ...
Cady Cirbes, Joseph M. Tanski
doaj   +1 more source

3-Hydroxyphenylacetic Acid Induces The Burkholderia cenocepacia Phenylacetic Acid Degradation Pathway. Towards Understanding The Contribution Of Aromatic Catabolism To Pathogenesis

open access: yesFrontiers in Cellular and Infection Microbiology, 2011
The phenylacetic acid (PA) degradative pathway is the central pathway by which complex aromatic compounds (e.g. styrene) get degraded. Upper pathways for different aromatic compounds converge at common intermediate phenylacetyl-CoA, which is then ...
Ijeme A Imolorhe, Silvia T Cardona
doaj   +1 more source

The Bacteriostatic Activity of 2-Phenylethanol Derivatives Correlates with Membrane Binding Affinity

open access: yesMembranes, 2021
The hydrophobic tails of aliphatic primary alcohols do insert into the hydrophobic core of a lipid bilayer. Thereby, they disrupt hydrophobic interactions between the lipid molecules, resulting in a decreased lipid order, i.e., an increased membrane ...
Isabel S. Kleinwächter   +6 more
doaj   +1 more source

Synthesis, Crystal Structure and Catalytic Activity of a Novel Ba(II) Complex with Pyridine-2-Carboxaldehyde-2-Phenylacetic Acid Hydrazone Ligand

open access: yesCrystals, 2017
A novel Ba(II) complex, [BaL2Cl2] (1) (L = pyridine-2-carboxaldehyde-2-phenylacetic acid hydrazone), has been synthesized using BaCl2, pyridine-2-carboxaldehyde and 2-phenylacetohydrazide as raw materials.
Li-Hua Wang   +3 more
doaj   +1 more source

Biotransformation and Production from Hansenula Anomala to Natural Ethyl Phenylacetate

open access: yesMATEC Web of Conferences, 2015
Ethyl phenylacetate can be widely applied in many industries, such as food, medicines, cosmetics and medicinal herbs. At the moment, the production of natural ethyl phenylacetate is very limited. However, the biotransformation production of natural ethyl
Tian Xun   +5 more
doaj   +1 more source

Isotelluroureas for Asymmetric C1 Ammonium Enolate Reactions

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Chiral isotelluroureas are powerful catalysts for a variety of C─C bond forming C1 ammonium enolate transformations. Isotelluroureas (ITeUs) have recently been introduced as a novel class of highly nucleophilic Lewis base catalysts. Herein, we systematically screened them for their potential to facilitate C1 ammonium enolate transformations and ...
Fereshteh Khorasani   +3 more
wiley   +1 more source

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