Results 151 to 160 of about 2,566,479 (206)
Some of the next articles are maybe not open access.
THE METABOLISM OF PHENYLACETIC ACID BY A PSEUDOMONAS
Canadian Journal of Microbiology, 1967A Pseudomonas species adapted to grow on phenylacetic acid is simultaneously adapted to the utilization of phenylacetic acid, p-hydroxyphenylacetic acid, and 3,4-dihydroxyphenylacetic acid. Extracts of the organism catalyze the oxidation of p-hydroxyphenylacetic acid and 3,4-dihydroxyphenylacetic acid, but not phenylacetic acid.
E R, Blakley +3 more
openaire +2 more sources
Dissociation constants of phenylacetic acid and three substituted phenylacetic acids
Journal of the Chemical Society B: Physical Organic, 1971The dissociation constants of four acids in aqueous solution have been determined at 25° by means of conductivity measurements. The pK values are: phenylacetic acid, 4·310; o-methylphenylacetic acid, 4·297; o-ethylphenylacetic acid, 4·317; o-fluorophenylacetic acid, 4·093.
Wayne C. Duer, R. A. Robinson
openaire +1 more source
Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 2011
The structural stability of phenylacetic acid and mandelic acid was investigated by the DFT-B3LYP and the ab initio MP2 calculations with the 6-311G** basis set. The two molecules were predicted at the DFT and MP2 levels of calculation to have the non-planar (Np) forms as their lowest energy structures.
Hassan Badawi, Wolfgang Forner
exaly +3 more sources
The structural stability of phenylacetic acid and mandelic acid was investigated by the DFT-B3LYP and the ab initio MP2 calculations with the 6-311G** basis set. The two molecules were predicted at the DFT and MP2 levels of calculation to have the non-planar (Np) forms as their lowest energy structures.
Hassan Badawi, Wolfgang Forner
exaly +3 more sources
Acid Strengths of the Phenylacetic Acids
Journal of The Electrochemical Society, 1953The ratio of dissociation constants Ksubstituted acid/Kacetic acid was determined in methanol and ethanol for mono‐, di‐, and triphenylacetic acid by the electrometric and colorimetric methods. In water, the insolubility of triphenylacetic made another procedure necessary with that acid, and the solubility method of Lowenherz was employed.
Mary L. Kilpatrick, Edward Fackenthal
openaire +1 more source
Synthesis of phenylacetic acid by carbonylation
Journal of Molecular Catalysis A, 2000The carbonylation of benzyl alcohol to phenylacetic acid and its derivatives in the presence of rhodium catalysts is reported in this work. The influence of different reaction conditions, such as total reaction pressure, hydrogen partial pressure, catalyst, promoter and reactant concentrations, as well as reaction temperature on the catalytic activity ...
Qing-Hua Fan
exaly +2 more sources
Phenylacetic acid derivatives as hPPAR agonists
Bioorganic & Medicinal Chemistry Letters, 2003Beginning with the weakly active lead structure 1, a new series of hPPAR agonists was developed. In vivo glucose and triglyceride lowering activity was obtained by homologation and oxamination to 3, then conversion to substituted benzisoxazoles 4 and 5. Further manipulation afforded benzofurans 6 and 7. Compound 7 was of comparable potency as a glucose
Conrad, Santini +10 more
openaire +2 more sources
The conjugation of benzoic acid and phenylacetic acid by the pipistrelle bat
Comparative Biochemistry and Physiology Part C: Comparative Pharmacology, 1977Abstract 1. British Pipistrelle bats dosed with 14C-labelled benzoic acid produced a single metabolite, hippuric acid, in contrast to the Indian fruit bat which appears unable to synthesize this conjugate. 2. 14C-labelled phenylacetic acid was also conjugated with glycine in the Pipistrelle bat, which compares with the Asian, African and South ...
M M, Angelo, J R, Idle
openaire +2 more sources
Acta Crystallographica Section C Crystal Structure Communications, 1991
D. J. Hodgson, R. O. Asplund
openaire +1 more source
D. J. Hodgson, R. O. Asplund
openaire +1 more source
Oxidation of phenylacetic acid by a Pseudomonas
Biochimica et Biophysica Acta (BBA) - Enzymology and Biological Oxidation, 1965S, DAGLEY, J M, WOOD
openaire +2 more sources

