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Journal articles on the topic 'Phenylacetic acids'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Lamas-Maceiras, Mónica, Inmaculada Vaca, Esther Rodríguez, Javier Casqueiro, and Juan F. Martín. "Amplification and disruption of the phenylacetyl-CoA ligase gene of Penicillium chrysogenum encoding an aryl-capping enzyme that supplies phenylacetic acid to the isopenicillin N-acyltransferase." Biochemical Journal 395, no. 1 (2006): 147–55. http://dx.doi.org/10.1042/bj20051599.

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A gene, phl, encoding a phenylacetyl-CoA ligase was cloned from a phage library of Penicillium chrysogenum AS-P-78. The presence of five introns in the phl gene was confirmed by reverse transcriptase-PCR. The phl gene encoded an aryl-CoA ligase closely related to Arabidopsis thaliana 4-coumaroyl-CoA ligase. The Phl protein contained most of the amino acids defining the aryl-CoA (4-coumaroyl-CoA) ligase substrate-specificity code and differed from acetyl-CoA ligase and other acyl-CoA ligases. The phl gene was not linked to the penicillin gene cluster. Amplification of phl in an autonomous repli

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2

Drmanic, Sasa, Bratislav Jovanovic, and Milica Misic-Vukovic. "A comparative LFER study of the reactivity of pyridineacetic, pyridineacetic acids N-oxide and substituted phenylacetic acids with diazodiphenylmethane in various alcohols." Journal of the Serbian Chemical Society 65, no. 12 (2000): 847–56. http://dx.doi.org/10.2298/jsc0012847d.

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Rate constants have been determined for the reactions of diazodiphenylmethane (DDM) with 3- and 4-pyridineacetic acid, 3- and 4-pyridineacetic acid N-oxide and some meta- and para-substituted phenylacetic acids in twelve alcohols. The determined rate constants, together with literature data, were used for calculation of Hammett ? values in a series of alcohols. Secondary ? constants have been calculated for substituents in meta and para-position of phenylacetic acids not given in literature, and also ? constants for 3N, 3N-O, 4N and 4N-O in pyridineacetic acids, in alcohols used. The transmiss

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3

Ribeiro da Silva, Manuel A. V., Ana I. M. C. Lobo Ferreira, Luı´s M. Spencer S. Lima, and Sandra M. M. Sousa. "Thermochemistry of phenylacetic and monochlorophenylacetic acids." Journal of Chemical Thermodynamics 40, no. 2 (2008): 137–45. http://dx.doi.org/10.1016/j.jct.2007.07.010.

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4

Kamat, Shrivallabh P., Asha M. D'Souza, Shashikumar K. Paknikar, and Philip S. Beauchamp. "A Convenient One-Pot Synthesis of 4-Methyl-3-Phenyl-, 3-Aryl- and 3-Aryl-4-Phenylcoumarins." Journal of Chemical Research 2002, no. 5 (2002): 242–46. http://dx.doi.org/10.3184/030823402103171834.

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Thermal condensation of 2′-hydroxyacetophenones 1a–e with phenylacetic acid 2a in refluxing diphenyl ether gives 4-methyl-3-phenylcoumarins 3a–e. Similarly, reaction of 2-hydroxybenzaldehydes 1f–m and 2-hydroxybenzo-phenones 1n–p with phenylacetic acids 2a–d gives the corresponding 3-arylcoumarins 3f–m and 3-aryl-4-phenylcoumarins 3n–p respectively. Formation of esters 4 and 5 and benzofuran 6 is also observed.

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5

Do, Nhan T., Khoa M. Tran, Hao T. Phan, Tuong A. To, Tung T. Nguyen, and Nam T. S. Phan. "Functionalization of activated methylene C–H bonds with nitroarenes and sulfur for the synthesis of thioamides." Organic & Biomolecular Chemistry 17, no. 40 (2019): 8987–91. http://dx.doi.org/10.1039/c9ob01751h.

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6

Wang, Xinchao, Hang Wang, Chunlin Zhou, Lei Yang, Lei Fu, and Gang Li. "Native carboxyl group-assisted C–H acetoxylation of hydrocinnamic and phenylacetic acids." Chemical Communications 58, no. 32 (2022): 4993–96. http://dx.doi.org/10.1039/d2cc00459c.

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7

Serra, Stefano, Antonio Castagna, Stefano Marzorati, and Mattia Valentino. "Biotransformation of the Proteogenic Amino Acids Phenylalanine, Tyrosine and Tryptophan by Yarrowia Species: An Application to the Preparative Synthesis of Natural Phenylacetic Acid." Catalysts 12, no. 12 (2022): 1638. http://dx.doi.org/10.3390/catal12121638.

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The biotransformation of the aromatic amino acids phenylalanine, tyrosine and tryptophan originates a number of bioactive compounds. Yeasts are the most used microorganisms for the transformation of (L)-phenylalanine into the flavour phenylethanol. Here, we reported a study on the biotransformation of the proteogenic aminoacids phenylalanine, tyrosine and tryptophan by yeast strains belonging to Yarrowia genus. We found that the latter microorganisms, in high aerobic conditions, metabolise the aromatic amino acids (L)-phenylalanine and (L)-tyrosine with the almost exclusive formation of phenyl

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8

Pinto, Andrea, Immacolata Serra, Diego Romano, et al. "Preparation of Sterically Demanding 2,2-Disubstituted-2-Hydroxy Acids by Enzymatic Hydrolysis." Catalysts 9, no. 2 (2019): 113. http://dx.doi.org/10.3390/catal9020113.

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Preparation of optically-pure derivatives of 2-hydroxy-2-(3-hydroxyphenyl)-2-phenylacetic acid of general structure 2 was accomplished by enzymatic hydrolysis of the correspondent esters. A screening with commercial hydrolases using the methyl ester of 2-hydroxy-2-(3-hydroxyphenyl)-2-phenylacetic acid (1a) showed that crude pig liver esterase (PLE) was the only preparation with catalytic activity. Low enantioselectivity was observed with substrates 1a–d, whereas PLE-catalysed hydrolysis of 1e proceeded with good enantioselectivity (E = 28), after optimization. Enhancement of the enantioselecti

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9

Grieb, Paweł, Tomasz Kryczka, Radosław Wójtowicz, Jerzy Kawiak, and Zygmunt Kazimierczuk. "5'-Esters of 2'-deoxyadenosine and 2-chloro-2'-deoxyadenosine with cell differentiation-provoking agents." Acta Biochimica Polonica 49, no. 1 (2002): 129–37. http://dx.doi.org/10.18388/abp.2002_3829.

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Phenylacetic and retinoic acids are carboxyacidic cell differentiating agents displaying anticancer activities. We report on a new class of compounds including the 5'-esters of 2'-deoxyadenosine (dA) or 2-chloro-2'-deoxyadenosine (cladribine, 2CdA) and the aforementioned acids. The rationale behind the synthesis of these esters was that if they are hydrolyzed inside the lymphoid cells, either dA will be removed from the intracellular environment by deamination, or 2CdA will be phosphorylated and accumulated. In either case targetted delivery of the differentiating agent to the lymphoid cells m

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10

Mohamed, Magdy, Wael Ismail, Johann Heider, and Georg Fuchs. "Aerobic metabolism of phenylacetic acids in Azoarcus evansii." Archives of Microbiology 178, no. 3 (2002): 180–92. http://dx.doi.org/10.1007/s00203-002-0438-y.

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11

Deng, Leiling, Bin Huang, and Yunyun Liu. "Copper(ii)-mediated, carbon degradation-based amidation of phenylacetic acids toward N-substituted benzamides." Organic & Biomolecular Chemistry 16, no. 9 (2018): 1552–56. http://dx.doi.org/10.1039/c8ob00064f.

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The carbon degradation-based amidation of phenylacetic acids with aryl amides has been realized in the presence of Cu(OAc)<sub>2</sub>, which provides a practical route in the synthesis of N-aryl secondary benzamides.

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12

Koetsier, Martijn J., Peter A. Jekel, Marco A. van den Berg, Roel A. L. Bovenberg, and Dick B. Janssen. "Characterization of a phenylacetate–CoA ligase from Penicillium chrysogenum." Biochemical Journal 417, no. 2 (2008): 467–76. http://dx.doi.org/10.1042/bj20081257.

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Enzymatic activation of PAA (phenylacetic acid) to phenylacetyl-CoA is an important step in the biosynthesis of the β-lactam antibiotic penicillin G by the fungus Penicillium chrysogenum. CoA esters of PAA and POA (phenoxyacetic acid) act as acyl donors in the exchange of the aminoadipyl side chain of isopenicillin N to produce penicillin G or penicillin V. The phl gene, encoding a PCL (phenylacetate–CoA ligase), was cloned in Escherichia coli as a maltose-binding protein fusion and the biochemical properties of the enzyme were characterized. The recombinant fusion protein converted PAA into p

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13

Nedev, Hinyu N., Neiko M. Stoyanov, Stoyan Minchev, and Boris V. Aleksiev. "Synthesis of 5,7-Dioxo-6-halogenophenyl-6,7-dihydro-5H-dibenzo[a,c]cycloheptene Derivatives." Collection of Czechoslovak Chemical Communications 57, no. 5 (1992): 1081–84. http://dx.doi.org/10.1135/cccc19921081.

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The condensation of diphenic anhydride with o-, m- and p- halogenosubstituted phenylacetic acids gave the respective enolacetates Ia-Ie. The alkaline hydrolysis of these compounds yields the diketones IIa-IIe. After testing blood cloting agents in vivo, the last compounds showed indications of anticoagulants.

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14

Burns, Misty-Dawn, and Matthew Lukeman. "Efficient Photodecarboxylation of Trifluoromethyl-substituted Phenylacetic and Mandelic Acids." Photochemistry and Photobiology 86, no. 4 (2010): 821–26. http://dx.doi.org/10.1111/j.1751-1097.2010.00737.x.

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15

Giroux, André, Christian Nadeau, and Yongxin Han. "Synthesis of phenylacetic acids under rhodium-catalyzed carbonylation conditions." Tetrahedron Letters 41, no. 40 (2000): 7601–4. http://dx.doi.org/10.1016/s0040-4039(00)01327-7.

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16

Navid, Keary. "igand-Accelerated ortho-C-H Olefination of Phenylacetic Acids." Organic Syntheses 92 (2015): 58–75. http://dx.doi.org/10.15227/orgsyn.092.0058.

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17

Snook, M. E., P. F. Mason, R. F. Arrendale, and O. T. Chortyk. "Capillary gas chromatography of dihydroxybenzoic, -phenylacetic and -phenylpropionic acids." Journal of Chromatography A 324 (January 1985): 141–51. http://dx.doi.org/10.1016/s0021-9673(01)81313-3.

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18

Arfmann, Hans-Adolf, and Wolf-Rainer Abraham. "Microbial Reduction of Aromatic Carboxylic Acids." Zeitschrift für Naturforschung C 48, no. 1-2 (1993): 52–57. http://dx.doi.org/10.1515/znc-1993-1-210.

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Several benzoic, cinnamic and phenylacetic acid derivatives were screened with 20 microorganisms, mainly fungi, for the reduction of their carboxylic function. For all organisms several compounds were reduced in fairly good yields up to 80% to the corresponding alcohol. No general rule could be established, concerning the substitution pattern, as to which compounds were transformed to the alcohol. Generally the reactions were accomplished within 48-70h. Only minor, if any, side products were detected. Dicarboxylic acids, such as phthalic or phenylglutaric acids and similar compounds could not

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19

Le, Thu N. M., Son H. Doan, Phuc H. Pham, et al. "Synthesis of triphenylpyridines via an oxidative cyclization reaction using Sr-doped LaCoO3 perovskite as a recyclable heterogeneous catalyst." RSC Advances 9, no. 41 (2019): 23876–87. http://dx.doi.org/10.1039/c9ra04096j.

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An La<sub>0.6</sub>Sr<sub>0.4</sub>CoO<sub>3</sub> strontium-doped lanthanum cobaltite perovskite was prepared via a gelation and calcination approach and used as a heterogeneous catalyst for the synthesis of triphenylpyridines via the cyclization reaction between ketoximes and phenylacetic acids.

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20

Rustamov, Mahmud, Shukufa Eyvazova, Naila Veysova, and Gulnaz Mirzayeva. "ELECTROPHYLIC REACTIONS OF CHLOROCARBOXYLIC ANHYDRIDE OF 1-METHYL-CYCLOHEX-3-ENE WITH 3-OXINDOLE AND N-PHENYLACETIC ACID." Elmi Əsərlər 11, no. 1 (2023): 77–81. http://dx.doi.org/10.61413/cksb9562.

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The properties of various functionally substituted nitrogen-organic com- pounds depend on their structure, the state and nature of the functional group in their molecule. Functionally substituted proteins obtained on the basis of the peptide bond of substituted heterocyclic compounds from various amino acids perform a physiological function that is widespread in nature and is important for the vital activity of the body. The direct acidification reaction of aromatic amines with aromatic carboxylic acids takes place under severe conditions at temperatures above 2800 C, the product is obtained w

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21

Werstiuk, Nick Henry, and George Timmins. "Preparation of deuterium labelled styrenes and divinylbenzenes." Canadian Journal of Chemistry 64, no. 6 (1986): 1072–76. http://dx.doi.org/10.1139/v86-179.

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Specifically deuteriated styrenes (1-d, 2,2′-d2, and ring labelled), perdeuteriostyrene, and specifically deuteriated divinylbenzenes (1,1′-d2,2,2,2′,2′-d4, and ring labelled) have been prepared by transforming suitably labelled phenylacetic (hydride or deuteride reduction and dehydration by solid KOH) and phenylenediacetic acids (esterification, hydride or deuteride reduction, and dehydration by solid KOH), respectively.

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22

Bartalucci, Niccolò, Fabio Marchetti, Stefano Zacchini, and Guido Pampaloni. "Decarbonylation of phenylacetic acids by high valent transition metal halides." Dalton Transactions 48, no. 17 (2019): 5725–34. http://dx.doi.org/10.1039/c9dt00551j.

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23

Milne, Jacqueline E., Thomas Storz, John T. Colyer, et al. "Iodide-Catalyzed Reductions: Development of a Synthesis of Phenylacetic Acids." Journal of Organic Chemistry 76, no. 22 (2011): 9519–24. http://dx.doi.org/10.1021/jo2018087.

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24

Dinoiu, Vasile, Tsuyoshi Fukuhara, Kaori Miura, and Norihiko Yoneda. "Electrochemical partial fluorination of phenylacetic acids esters and 1-tetralone." Journal of Fluorine Chemistry 121, no. 2 (2003): 227–31. http://dx.doi.org/10.1016/s0022-1139(03)00037-x.

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25

Li, Gen-Cheng, Peng Wang, Marcus E. Farmer, and Jin-Quan Yu. "Ligand-Enabled Auxiliary-Freemeta-C−H Arylation of Phenylacetic Acids." Angewandte Chemie 129, no. 24 (2017): 6978–81. http://dx.doi.org/10.1002/ange.201702686.

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26

Li, Gen-Cheng, Peng Wang, Marcus E. Farmer, and Jin-Quan Yu. "Ligand-Enabled Auxiliary-Freemeta-C−H Arylation of Phenylacetic Acids." Angewandte Chemie International Edition 56, no. 24 (2017): 6874–77. http://dx.doi.org/10.1002/anie.201702686.

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27

A., B. SEN, and M. BHARGAVA P. "SYNTHESIS OF SUBSTITUTED DINITROPHENYL KETONES AND PHENYLACETIC ACIDS. PART II." Journal of Indian Chemical Society Vol. 24, Jan-Dec 1947 (2022): 371–72. https://doi.org/10.5281/zenodo.6592110.

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28

Jerković, Igor, Zvonimir Marijanović, Marina Kranjac, and Ani Radonić. "Comparison of Different Methodologies for Detailed Screening of Taraxacum officinale Honey Volatiles." Natural Product Communications 10, no. 2 (2015): 1934578X1501000. http://dx.doi.org/10.1177/1934578x1501000238.

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Headspace solid-phase microextraction (HS-SPME), ultrasonic solvent extraction (USE) and solid phase extraction (SPE), followed by GC-FID/MS were used for screening of dandelion ( Taraxacum officinale Weber) honey headspace, volatiles and semi-volatiles. The obtained results constitute a breakthrough towards screening of dandelion honey since dominant compounds identified in the extracts were not previously reported for this honey type. Nitriles dominated in the headspace, particularly 3-methylpentanenitrile (up to 29.9%) and phenylacetonitrile (up to 20.9%). Lower methyl branched aliphatic ac

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29

Lee, Young-Hoon, Mi-Hye Seong, Kwon-Yub Lee, Song-Hee Choi, and Jin-Burm Kyong. "Application of the Extended Grunwald-Winstein Equation to Solvolyses of (Bromomethyl)phenylacetic Acids." Journal of the Korean Chemical Society 54, no. 3 (2010): 354–58. http://dx.doi.org/10.5012/jkcs.2010.54.3.354.

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30

Murdoch, Robert W., and Anthony G. Hay. "Formation of Catechols via Removal of Acid Side Chains from Ibuprofen and Related Aromatic Acids." Applied and Environmental Microbiology 71, no. 10 (2005): 6121–25. http://dx.doi.org/10.1128/aem.71.10.6121-6125.2005.

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ABSTRACT Although ibuprofen [2-(4-isobutylphenyl)-propionic acid] is one of the most widely consumed drugs in the world, little is known regarding its degradation by environmental bacteria. Sphingomonas sp. strain Ibu-2 was isolated from a wastewater treatment plant based on its ability to use ibuprofen as a sole carbon and energy source. A slight preference toward the R enantiomer was observed, though both ibuprofen enantiomers were metabolized. A yellow color, indicative of meta-cleavage, accumulated transiently in the culture supernatant when Ibu-2 was grown on ibuprofen. When and only when

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31

Cuervo, Lorena, Patrick L. McAlpine, Carlos Olano, Javier Fernández, and Felipe Lombó. "Low-Molecular-Weight Compounds Produced by the Intestinal Microbiota and Cardiovascular Disease." International Journal of Molecular Sciences 25, no. 19 (2024): 10397. http://dx.doi.org/10.3390/ijms251910397.

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Cardiovascular disease is the main cause of mortality in industrialized countries, with over 500 million people affected worldwide. In this work, the roles of low-molecular-weight metabolites originating from the gut microbiome, such as short-chain fatty acids, hydrogen sulfide, trimethylamine, phenylacetic acid, secondary bile acids, indoles, different gases, neurotransmitters, vitamins, and complex lipids, are discussed in relation to their CVD-promoting or preventing activities. Molecules of mixed microbial and human hepatic origin, such as trimethylamine N-oxide and phenylacetylglutamine,

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32

Basha, G. Mahaboob, S. Kumar Yadav, R. Srinuvasarao, et al. "A mild and efficient protocol to synthesize chromones, isoflavones, and homoisoflavones using the complex 2,4,6-trichloro-1,3,5-triazine/dimethylformamide." Canadian Journal of Chemistry 91, no. 8 (2013): 763–68. http://dx.doi.org/10.1139/cjc-2013-0137.

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A mild and efficient one-flask method has been developed for the synthesis of chromones, isoflavones, and homoisoflavones from 2-hydroxyacetophenones, deoxybenzoins, and dihydrochalcones, respectively, via one-carbon extension using the complex 2,4,6-trichloro-1,3,5-triazine/dimethylformamide. Deoxybenzoins and dihydrochalcones were prepared in situ by the reaction of readily available substituted phenols with phenylacetic acids and 3-phenylpropanoic acids, respectively. This method allows the synthesis of a wide range of compounds with multiple phenolic hydroxyls and other substituents. The m

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33

Hasegawa, Yuko, Yoko Morita, Masako Hase, and Mayumi Nagata. "Complexation of Lanthanoid(III) with Substituted Benzoic or Phenylacetic Acids and Extraction of These Acids." Bulletin of the Chemical Society of Japan 62, no. 5 (1989): 1486–91. http://dx.doi.org/10.1246/bcsj.62.1486.

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34

Aleu, J., G. Fronza, C. Fuganti, et al. "Differentiation of natural and synthetic phenylacetic acids by 2H NMR of the derived benzoic acids." European Food Research and Technology 214, no. 1 (2002): 63–66. http://dx.doi.org/10.1007/s002170100406.

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35

Lechner, Robert, Susanne Kümmel, and Burkhard König. "Visible light flavin photo-oxidation of methylbenzenes, styrenes and phenylacetic acids." Photochemical & Photobiological Sciences 9, no. 10 (2010): 1367. http://dx.doi.org/10.1039/c0pp00202j.

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36

Ali Badry, Mohamed Gomaa, Benson Kariuki, David W. Knight, and Mohammed F.K. "6-exo versus 7-endo iodolactonizations of 2-(alkynyl)phenylacetic acids." Tetrahedron Letters 50, no. 13 (2009): 1385–88. http://dx.doi.org/10.1016/j.tetlet.2008.12.097.

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37

Oelschlägel, Michel, Stefan R. Kaschabek, Juliane Zimmerling, Michael Schlömann, and Dirk Tischler. "Co-metabolic formation of substituted phenylacetic acids by styrene-degrading bacteria." Biotechnology Reports 6 (June 2015): 20–26. http://dx.doi.org/10.1016/j.btre.2015.01.003.

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38

Romano, Andrea, Raffaella Gandolfi, Francesco Molinari, Attilio Converti, Mario Zilli, and Marco Del Borghi. "Esterification of phenylacetic and 2-phenylpropionic acids by mycelium-bound carboxylesterases." Enzyme and Microbial Technology 36, no. 4 (2005): 432–38. http://dx.doi.org/10.1016/j.enzmictec.2004.08.042.

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39

Giroux, Andre, Christian Nadeau, and Yongxin Han. "ChemInform Abstract: Synthesis of Phenylacetic Acids under Rhodium-Catalyzed Carbonylation Conditions." ChemInform 31, no. 51 (2000): no. http://dx.doi.org/10.1002/chin.200051091.

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40

Daneshvar, Maryam I., John B. Brooks, Georgia B. Malcolm, and Leo Pine. "Analyses of fermentation products of Listeria species by frequency-pulsed electron-capture gas–liquid chromatography." Canadian Journal of Microbiology 35, no. 8 (1989): 786–93. http://dx.doi.org/10.1139/m89-131.

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Aerobic fermentation broths of eight Listeria monocytogenes strains, two or more strains of the remaining six Listeria species, and one strain of Jonesia denitrificans were examined by frequency-pulsed electron-capture gas–liquid chromatography for carboxylic acids, alcohols, amines, and hydroxy acids. All species produced acetic, isobutyric, butyric, isovaleric, phenylacetic, lactic, 2-hydroxybutyric, 2-hydroxyvaleric, and 2-hydroxyisocaproic acids. Propionic acid was not formed, and traces of isocaproic acid were observed. Of the alcohol and amine derivatives observed, only acetylmethylcarbi

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41

Wang, Yangyang, Xiaobo Xu, Gaorong Wu, Binghan Pang, Shaowen Liao, and Yafei Ji. "Ligand-Enabled C–H Olefination and Lactonization of Benzoic Acids and Phenylacetic Acids via Palladium Catalyst." Organic Letters 24, no. 3 (2022): 821–25. http://dx.doi.org/10.1021/acs.orglett.1c04000.

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42

Feng, Qiang, та Qiuling Song. "Aldehydes and Ketones Formation: Copper-Catalyzed Aerobic Oxidative Decarboxylation of Phenylacetic Acids and α-Hydroxyphenylacetic Acids". Journal of Organic Chemistry 79, № 4 (2014): 1867–71. http://dx.doi.org/10.1021/jo402778p.

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43

Cívicos, José, Paulo Costa та Jorge Domingos. "Palladium-Catalyzed α-Arylation of Dimethyl Malonate and Ethyl Cyanoacetate with o-Alkoxybromobenzenes for the Synthesis of Phenylacetic Acid, Esters and Phenylacetonitriles". SynOpen 01, № 01 (2017): 0091–96. http://dx.doi.org/10.1055/s-0036-1588550.

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α-Aryl malonate and α-aryl cyano acetate moieties are found in the structures of many bioactive compounds. They are also key intermediates for the synthesis of many compounds such as isoflavonoids. In this work, we synthesized these compounds, with different patterns of substitution, starting with the palladium-catalyzed reaction of o-alkoxy-bromoarenes with dimethyl malonate or ethyl cyanoacetate. Under the conditions applied, moderate to good yields of arylmalonate monoesters, phenylacetic esters or acids, and benzylnitrile derivatives were obtained.

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44

WATANABE, Katsuji, and Eiji TANIGUCHI. "Structure Activity Relationship of o-Substituted Phenylacetic Acids in Plant Growth Regulation." Journal of Pesticide Science 20, no. 1 (1995): 1–8. http://dx.doi.org/10.1584/jpestics.20.1.

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45

Dhanoa, Daljit S., Scott W. Bagley, Raymond S. L. Chang, et al. "(Dipropylphenoxy)phenylacetic acids: a new generation of nonpeptide angiotensin II receptor antagonists." Journal of Medicinal Chemistry 36, no. 23 (1993): 3738–42. http://dx.doi.org/10.1021/jm00075a033.

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46

Takemoto, Ichiki, Norio Kawamura та Hiroshi Kaminaka. "Synthesis of Optically Activeα-Isopropyl-4-substituted Phenylacetic Acids by Asymmetric Hydrogenation". Bioscience, Biotechnology, and Biochemistry 58, № 11 (1994): 2071–72. http://dx.doi.org/10.1271/bbb.58.2071.

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47

Reveneau, Carine, Sarah E. Adams, M. A. Cotta, and M. Morrison. "Phenylacetic and Phenylpropionic Acids Do Not Affect Xylan Degradation by Ruminococcus albus." Applied and Environmental Microbiology 69, no. 11 (2003): 6954–58. http://dx.doi.org/10.1128/aem.69.11.6954-6958.2003.

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ABSTRACT Since the addition of either ruminal fluid or a combination of phenylacetic and phenylpropionic acids (PAA/PPA) has previously been shown to dramatically improve cellulose degradation and growth of Ruminococcus albus, it was of interest to determine the effects of these additives on xylan-grown cultures. Although cell-bound xylanase activity increased when either PAA/PPA or ruminal fluid was added to the growth medium, total xylanase did not change, and neither of these supplements affected the growth or xylan-degrading capacity of R. albus 8. Similarly, neither PAA/PPA nor ruminal fl

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Radushev, Alexander, Vadim Gusev, and Vera Vaulina. "Extraction of Copper(II) withN′,N′-Dialkylhydrazides of Benzoic and Phenylacetic Acids." Separation Science and Technology 46, no. 10 (2011): 1665–72. http://dx.doi.org/10.1080/01496395.2011.575428.

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Milne, Jacqueline E., Thomas Storz, John T. Colyer, et al. "ChemInform Abstract: Iodide-Catalyzed Reductions: Development of a Synthesis of Phenylacetic Acids." ChemInform 43, no. 12 (2012): no. http://dx.doi.org/10.1002/chin.201212045.

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Mori, Takamichi, Yusuke Akioka, Hisaho Kawahara, Ryo Ninokata, Gen Onodera, and Masanari Kimura. "Efficient and Selective Formation of Unsaturated Carboxylic and Phenylacetic Acids from Diketene." Angewandte Chemie International Edition 53, no. 39 (2014): 10434–38. http://dx.doi.org/10.1002/anie.201404816.

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