Relevant bibliographies by topics / Chlorophenylacetic Acid

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Academic literature on the topic 'Chlorophenylacetic Acid'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Chlorophenylacetic Acid"

1

Mi, A. Q., Z. Y. Wang, and Y. Z. Jiang. "Asymmetric catalytic alkylation of 4-chlorophenylacetic acid." Tetrahedron: Asymmetry 4, no. 9 (1993): 1957–60. http://dx.doi.org/10.1016/s0957-4166(00)82238-7.

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2

Morano, Camillo, Alessandro Giraudo, Gabriella Roda та ін. "Efficient α-selective chlorination of phenylacetic acid and its para-substituted analogues". RSC Advances 15, № 16 (2025): 12298–303. https://doi.org/10.1039/d5ra00198f.

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MI, A. Q., Z. Y. WANG, and Y. Z. JIANG. "ChemInform Abstract: Asymmetric Catalytic Alkylation of 4-Chlorophenylacetic Acid." ChemInform 25, no. 2 (2010): no. http://dx.doi.org/10.1002/chin.199402147.

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4

Aputen, Angelico D., Maria George Elias, Jayne Gilbert, et al. "Bioactive Platinum(IV) Complexes Incorporating Halogenated Phenylacetates." Molecules 27, no. 20 (2022): 7120. http://dx.doi.org/10.3390/molecules27207120.

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A new series of cytotoxic platinum(IV) complexes (1–8) incorporating halogenated phenylacetic acid derivatives (4-chlorophenylacetic acid, 4-fluorophenylacetic acid, 4-bromophenylacetic acid and 4-iodophenylacetic acid) were synthesised and characterised using spectroscopic and spectrometric techniques. Complexes 1–8 were assessed on a panel of cell lines including HT29 colon, U87 glioblastoma, MCF-7 breast, A2780 ovarian, H460 lung, A431 skin, Du145 prostate, BE2-C neuroblastoma, SJ-G2 glioblastoma, MIA pancreas, the ADDP-resistant ovarian variant, and the non-tumour-derived MCF10A breast lin
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5

Stuhr, Anna, Sarah Hofmann, Michael Schlömann, and Michel Oelschlägel. "Investigation of the co-metabolic transformation of 4-chlorostyrene into 4-chlorophenylacetic acid in Pseudomonas fluorescens ST." Biotechnology Reports 18 (June 2018): e00248. http://dx.doi.org/10.1016/j.btre.2018.e00248.

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6

Huang, Hua, and Haizhen Yang. "Solubility of 2-Chlorophenylacetic Acid in 12 Pure Solvents from T = (273.15/283.15 to 318.15) K: Determination and Modeling." Journal of Chemical & Engineering Data 63, no. 8 (2018): 2790–803. http://dx.doi.org/10.1021/acs.jced.8b00139.

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7

Cikalov, V., V. Cikalova, A. Poddubov, and U. Guseynova. "SYNTHESIS AND POTENTIAL BIOLOGICAL ACTIVITY OF ANALOGUES OF THE DIBAZOL." Scientific Notes of V.I. Vernadsky Crimean Federal University. Biology. Chemistry 10, no. 3 (2024): 334–40. https://doi.org/10.29039/2413-1725-2024-10-3-334-340.

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The synthesis of benzimidazole derivatives, similar to dibazole, was carried out using two methods. According to the first, 1, 2-Phenylenediamine condensed with excess quantity of 2-chlorophenylacetic acid in the presence of orthoboric acid at a temperature of 150 °C. After treatment and crystallization, the yield of 2-(2-chlorobenzyl)-1H-benzimidazole was 36 %. In the second method, 1, 2-phenylenediamine was reacted with an excess of phenoxyacetic acid and 1-naphthylacetic acid in the presence of orthoboric acid in an o-xylene solvent at boiling point. Thus, 2-(phenoxymethyl)-1H-benzimidazole
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8

Wen, Liyuan, Handong Yin, Wenkuan Li, and Daqi Wang. "New organoantimony complexes with the isomers of chlorophenylacetic acid: Syntheses, characterizations and crystal structures of 1D polymeric chain, 2D network structure and 3D framework." Inorganica Chimica Acta 363, no. 4 (2010): 676–84. http://dx.doi.org/10.1016/j.ica.2009.11.022.

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9

Ravelli, Davide, Stefano Protti та Maurizio Fagnoni. "Photogenerated α,n-Didehydrotoluenes from Chlorophenylacetic Acids at Physiological pH". Journal of Organic Chemistry 80, № 2 (2014): 852–58. http://dx.doi.org/10.1021/jo502318v.

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10

Janczak, Jan. "Supramolecular solid-state architectures formed by co-crystallization of melamine and 2-, 3- and 4-chlorophenylacetic acids." Journal of Molecular Structure 1125 (December 2016): 493–502. http://dx.doi.org/10.1016/j.molstruc.2016.07.022.

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Book chapters on the topic "Chlorophenylacetic Acid"

1

Holze, Rudolf. "Ionic conductance of o-chlorophenylacetic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_537.

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2

Holze, Rudolf. "Ionic conductance of m-chlorophenylacetic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_538.

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3

Holze, Rudolf. "Ionic conductance of p-chlorophenylacetic acid." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_539.

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