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Journal articles on the topic 'Benzoic acid derivatives'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 February 2022

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1

Gorokhova, Larisa G., Nadezhda N. Mikhailova, Evgeniya V. Ulanova, and Tatyana K. Yadykina. "Assessment of the toxicity of benzoic acid derivatives in the intragastric intake." Hygiene and sanitation 99, no. 7 (2020): 755–60. http://dx.doi.org/10.47470/0016-9900-2020-99-7-755-760.

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Introduction. Benzoic acid and its numerous derivatives are widely used in all areas of chemical production. However, there is no information about the toxic properties of a large number of benzoic acid derivatives. The purpose of the study was to study the toxic properties of several derivatives of benzoic acids in intragastric intake in an experiment.Material and methods. The following derivatives of benzoic acid were studied: 4-chlorobenzoic, 4-methoxybenzoic, p-acetoxybenzoic and 2-methoxy-5-sulfamoylbenzoic acids. The studies were performed on white laboratory rats; toxicity was studied i

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2

Kulhánek, Jiří, and Oldřich Pytela. "Chemometric Analysis of Substituent Effects. XI. Solvent Effects on Dissociation of 2,6-Disubstituted Benzoic Acids." Collection of Czechoslovak Chemical Communications 62, no. 6 (1997): 913–24. http://dx.doi.org/10.1135/cccc19970913.

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Eleven symmetrically 2,6-disubstituted benzoic acids (with the following substituents: OCH3, OC2H5, OC3H7, OCH(CH3)2, OC4H9, CH3, F, Cl, Br, I, and NO2) have been synthesized and their dissociation constants measured potentiometrically in methanol, ethanol, propan-1-ol, propan-2-ol, butan-2-ol, acetone, dimethyl sulfoxide, dimethylformamide, acetonitrile, pyridine, and 1,2-dichloroethane. The experimental data obtained have been analyzed from the point of view of solvent effects on acidity of the individual derivatives. Different behaviour found with benzoic acid and the disubstituted derivati

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3

Mistry, Rakesh N., and K. R. Desai. "Studies on Synthesis of Some Novel Heterocyclic Azlactone Derivatives and Imidazolinone Derivatives and their Antimicrobial Activity." E-Journal of Chemistry 2, no. 1 (2005): 42–51. http://dx.doi.org/10.1155/2005/542938.

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p- Methyl benzoic acid on reaction with phosphorus pentachloride gives p - methyl benzoyl chloride derivative which on condensation with glycine gives p - methyl benzoyl glycine derivative. Now, this p - methyl benzoyl glycine derivative on condensation with various substituted aldehydes gives corresponding substituted 4 - [aryl methylidine] - 2 - [p - methyl phenyl] - oxazole - 5 - one derivatives [1(a-j)]. Further, these derivatives [1(a-j)] on condensation with 4 , 4’ - diamino diphenyl sulphone gives corresponding substituted imidazolinone - dibenzsulphone derivatives [2(a-j)], on condensa

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4

Synowiec, Alicja, Kinga Żyła, Małgorzata Gniewosz, and Marek Kieliszek. "An effect of positional isomerism of benzoic acid derivatives on antibacterial activity against Escherichia coli." Open Life Sciences 16, no. 1 (2021): 594–601. http://dx.doi.org/10.1515/biol-2021-0060.

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Abstract This study demonstrated the effect of positional isomerism of benzoic acid derivatives against E. coli ATCC 700728 with the serotype O157. The addition of hydroxyl and methoxyl substituents weakened the effect of acids against E. coli with respect to benzoic acid (except 2-hydroxybenzoic). The connection of the hydroxyl group at the second carbon atom in the benzoic ring reduced the time needed to kill bacterial cells. Phenolic acids with methoxyl substitutes limited the biofilm formation by E. coli to a greater extent than hydroxyl derivatives. The most significant influence on the a

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5

Kurfürst, Antonín, Pavel Lhoták, Petr Nádeník, Františka Raclová-Pavlíková, and Josef Kuthan. "2-(Biphenyl-4-yl)-5-phenyl-1,3,4-oxadiazole (PBD): Electrophilic 4’-substitution and following transformations." Collection of Czechoslovak Chemical Communications 56, no. 7 (1991): 1495–504. http://dx.doi.org/10.1135/cccc19911495.

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PBD was converted into 4’-substituted derivatives I-XII using usual electrophilic reagents. The decomposition of PBD, 4’-acetyl derivative I and 4’-nitro derivative VI with hydroiodic acid gave 4’-substituted 4-biphenylcarboxylic acids XIIIa-XIIIc and benzoic acid, respectively. The regioselectivity of the reaction was also proved by means of high resolution NMR spectroscopy.

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6

., MEETA, PRADEEP KUMAR, and BALASUBRAMANIAN NARASIMHAN. "Synthesis, antimicrobial evaluation and QSAR studies of p-amino benzoic acid derivatives." Journal of Pharmaceutical Technology, Research and Management 2, no. 1 (2014): 87–104. http://dx.doi.org/10.15415/jptrm.2014.21007.

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7

Sharma, Omprakash, Pankaj Sharma, Birendra Shrivastava, and Jitender Singh. "Synthesis and Antimicrobial evaluation of Azole Based (p-nitro Benzoic Acid) derivatives." Asian Pacific Journal of Health Sciences 5, no. 4 (2018): 54–60. http://dx.doi.org/10.21276/apjhs.2018.5.4.10.

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8

Ali, Zulfiqar, Viqar Uddin Ahmad, Muhammad Zahid, and Rasool Bakhsh Tareen. "Benzoic acid derivatives from Stocksia brahuica." Phytochemistry 48, no. 7 (1998): 1271–73. http://dx.doi.org/10.1016/s0031-9422(98)00124-1.

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9

Peleg, H., and A. C. Noble. "Perceptual Properties of Benzoic Acid Derivatives." Chemical Senses 20, no. 4 (1995): 393–400. http://dx.doi.org/10.1093/chemse/20.4.393.

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10

Chen, Bei, Kazuyoshi Kawazoe, Yoshihisa Takaishi, et al. "Prenylated Benzoic Acid Derivatives fromFerula kuhistanica." Journal of Natural Products 63, no. 3 (2000): 362–65. http://dx.doi.org/10.1021/np990338a.

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11

Tsevegsuren, N., P. Proksch, Y. Wang, and G. Davaakhuu. "Bioactive phenolic acids from Scorzonera radiata Fisch." Mongolian Journal of Chemistry 12 (September 24, 2014): 78–84. http://dx.doi.org/10.5564/mjc.v12i0.177.

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Chromatographic separation of the crude extract obtained from the aerial parts of the Mongolian medicinal plant Scorzonera radiata yielded five new dihydrostilbenes [4], two new flavonoids, one new quinic acid derivative, as well as twenty known compounds including eight quinic acid derivatives, four flavonoids, two coumarins, five simple benzoic acids, and one monoterpene glycoside. We present here results on isolation and structural identification some active phenolic compounds from the Scorzonera radiata - eight quinic acid derivatives (quinic acid, 4,5-dicaffeoylquinic acid, 4,5-dicaffeoyl

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12

Slobodianiuk, Oksana, Oleksandra Berezhnytska, Tetyana Kamens'ka, and Мария Русакова. "SYNTHESIS AND PROPERTIES OF NEW N-ACYL DERIVATIVES OF ANTHRANILIC ACID." Ukrainian Chemistry Journal 85, no. 4 (2019): 59–70. http://dx.doi.org/10.33609/0041-6045.85.4.2019.59-70.

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A series of N-acyl derivatives of anthranil (or o -aminobenzoic acid) was first synthesized, namely 2-(4-octylbenzamido)benzoic acid, 2-(4-(heptyloxy)- benzamido)benzoic acid, 2-(4-(heptylsulfanyl)benz-amido)benzoic acid. 2-(4-octylbenzamido)benzoic acid was synthesized in five stages of octylbenzene, by acylating chloride acid using a Friedie-Crafts reaction. 2-(4-(heptyloxy)benzamido)benzoic acid was prepared from the methyl ester of p-hydroxybenzoic acid which, at the first stage, was activated with 1-bromoheptane in acetonitrile with potassium carbonate and catalytic amount of sodium iodid

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13

Menezes, E., F. Santos, A. Velho, et al. "153 Sperm metabolomic landscape associated with bull fertility." Reproduction, Fertility and Development 31, no. 1 (2019): 201. http://dx.doi.org/10.1071/rdv31n1ab153.

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Sub-fertility fertility in bulls decreases the efficiency and profitability of cattle production because AI allows a single bull to inseminate thousands of cows. In recent decades, there has been a general decline in fertility of bulls, even among those exhibiting normal sperm motility and morphology. Despite advances in technology and knowledge, molecular, cellular and physiological mechanisms underlying the causes of low fertility in bulls are currently unclear. Therefore, the objective of this study was to identify sperm metabolites associated with fertility in Holstein bulls. The metabolom

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14

Miltojevic, Ana, and Niko Radulovic. "Complete assignment of 1H- and 13C-NMR spectra of anthranilic acid and its hydroxy derivatives and salicylic acid and its amino derivatives." Facta universitatis - series: Physics, Chemistry and Technology 13, no. 2 (2015): 121–32. http://dx.doi.org/10.2298/fupct1502121m.

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We report on the detailed NMR spectral analyses of amino- or/and hydroxy-substituted benzoic acids: anthranilic (AA), 3-hydroxyanthranilic (3-HAA), 5-hydroxyanthranilic (5-HAA), salicylic (SA), 4-aminosalicylic (4-ASA) and 5-aminosalicylic (5-ASA) acids. According to a literature survey, there are limited, unassigned or even incorrectly assigned spectral data to these benzoic acid derivatives. In order to amend the situation, a complete assignment of 1H- and 13C-NMR spectra of these compounds, recorded in perdeuteriodimethyl sulfoxide (DMSO-d6), based on a combination of 1D- and 2D-NMR experim

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15

Jeffrey, Christopher S., Michael D. Leonard, Andrea E. Glassmire, et al. "Antiherbivore Prenylated Benzoic Acid Derivatives fromPiper kelleyi." Journal of Natural Products 77, no. 1 (2014): 148–53. http://dx.doi.org/10.1021/np400886s.

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16

López, Andrés, Dong Sheng Ming, and G. H. Neil Towers. "Antifungal Activity of Benzoic Acid Derivatives fromPiperlanceaefolium." Journal of Natural Products 65, no. 1 (2002): 62–64. http://dx.doi.org/10.1021/np010410g.

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17

Kawahata, M., M. Kubokawa, T. Ishikawa, and K. Yamaguchi. "Cocrystals of monoguanidinobenzene with benzoic acid derivatives." Acta Crystallographica Section A Foundations of Crystallography 64, a1 (2008): C438. http://dx.doi.org/10.1107/s0108767308085930.

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18

Grell, Wolfgang, Rudolf Hurnaus, Gerhart Griss, et al. "Repaglinide and Related Hypoglycemic Benzoic Acid Derivatives." Journal of Medicinal Chemistry 41, no. 26 (1998): 5219–46. http://dx.doi.org/10.1021/jm9810349.

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19

Saleem, Mohd, Mohita Sharma, Simpy Mahajan, H. N. Sheikh, and B. L. Kalsotra. "Synthesis and Characterization of Group-6 Metal Carbonyl Complexes of Aroyl Hydrazone Derivatives." E-Journal of Chemistry 9, no. 2 (2012): 807–17. http://dx.doi.org/10.1155/2012/971981.

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Carbonyl complexes of Chromium, molybdenum and tungsten of composition, [M(CO)4L-L], (where M= Cr, Mo or W and L-L= benzoic acid[1-(Furan-2-yl)methylene]hydrazide (BFMH), benzoic acid[(thiophene-2-yl)methylene]hydrazide (BTMH), benzoic acid[1-(thiophene-2-yl)ethylidene] hydrazide (BTEH), benzoic acid (phenylmethylene)hydrazide (BPMH) and benzoic acid[1-(anisol-3-yl)methylene] hydrazide (BAMH) are reported. These have been prepared by refluxing metal carbonyls and the ligands in 1:1molar ratio. The complexes were characterized by elemental analysis, IR spectra, UV-vis spectra,1H NMR, TGA/DTA, c

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20

Petride, Horia, Constantin Drăghici, Cristina Florea, and Aurica Petride. "RuO4-mediated oxidation of N-benzylated tertiary amines. 3. Behavior of 1,4-dibenzylpiperazine and its oxygenated derivatives." Open Chemistry 4, no. 4 (2006): 674–94. http://dx.doi.org/10.2478/s11532-006-0039-8.

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Abstract1,4-Dibenzylpiperazine (1),-2-piperazinone (7),-2,6-piperazinedione (9), and 1-benzoyl-4-benzylpiperazine (30) were oxidized by RuO4 (generated in situ) by attack at their endocyclic and exocyclic (i.e., benzylic) aminic N-α-C-H bonds to afford various oxygenated derivatives, including acyclic diformamides, benzaldehyde, and benzoic acid. The reaction outcome was complicated by (i) the hydrolysis of diformamides, occurred during the work-up, and (ii) the reaction of benzaldehyde with the hydrolysis-derived amines giving imidazolidines and/or Schiff bases. Benzoic acid resulted from ben

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21

Alieva, M. N., and V. M. Farzaliyev. "Vapor-phase chromatography in glass-capillary column of high polar and involatile hydrocarbon-containing ether derivatives of disulpho-benzoic acid." Azerbaijan Oil Industry, no. 6 (June 15, 2020): 54–56. http://dx.doi.org/10.37474/0365-8554/2020-6-7-54-56.

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The paper deals with the results of capillary columns implementation in vapor-phase chromatography. Glass and narrow-bore columns covered with liquid stationary phase and polyphenyl ether were used, the mixtures of aliphatic alcohols, acids, amines and ether derivatives of disulpho-benzoic acid, which are semi-products of additive synthesis analyzed. The usage of water vapor as a moving carrier of nitrogen enabled to decrease the analysis time and improve division efficiency. The retention time, height values of equivalent theoretic plates and coefficient of analyzed components asymmetry were

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22

Ustinova, M. N., O. E. Lebedeva, and V. I. Kurdupova. "PHOTODESTRUCTIVE TRANSFORMATIONS OF BENZOIC ACID AND ITS DERIVATIVES." PROCEEDINGS OF UNIVERSITIES APPLIED CHEMISTRY AND BIOTECHNOLOGY 7, no. 4 (2017): 16–23. http://dx.doi.org/10.21285/2227-2925-2017-7-4-16-23.

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23

Park, Eun-Soo, Woong-Sig Moon, Min-Jin Song, Mal-Nam Kim, Kyoo-Hyun Chung, and Jin-San Yoon. "Antimicrobial activity of phenol and benzoic acid derivatives." International Biodeterioration & Biodegradation 47, no. 4 (2001): 209–14. http://dx.doi.org/10.1016/s0964-8305(01)00058-0.

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24

Flores, Ninoska, Ignacio A. Jiménez, Alberto Giménez, et al. "Benzoic Acid Derivatives fromPiperSpecies and Their Antiparasitic Activity." Journal of Natural Products 71, no. 9 (2008): 1538–43. http://dx.doi.org/10.1021/np800104p.

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25

Khasawneh, I. M., and J. D. Winefordner. "Fluorescence Quantum Efficiencies of Some Benzoic Acid Derivatives." Spectroscopy Letters 19, no. 4 (1986): 321–31. http://dx.doi.org/10.1080/00387018608069242.

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26

Świsłocka, R., E. Regulska, M. Samsonowicz, and W. Lewandowski. "Experimental and theoretical study on benzoic acid derivatives." Journal of Molecular Structure 1044 (July 2013): 181–87. http://dx.doi.org/10.1016/j.molstruc.2012.12.005.

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27

Kinchington, D., T. Ng, N. Mathews, M. Tisdale, D. Devine, and WO Ayuko. "T Cell Costimulation by Derivatives of Benzoic Acid." Antiviral Chemistry and Chemotherapy 8, no. 2 (1997): 121–30. http://dx.doi.org/10.1177/095632029700800206.

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A number of analogues of benzoic acid were evaluated in a T cell costimulation assay. One compound, the sodium salt of 2-chloro-5-nitrobenzoic acid (CNBA-Na) was chosen for further study and was found to be a potent costimulator of anti-CD3-induced proliferation of both H9 lymphoblastoid cells ( P<0.001) and human peripheral blood mononuclear cells ( P=0.001) in a dose-dependent manner. The costimulatory effect of CNBA-Na on CD3-triggered DNA synthesis did not enhance human immunodeficiency virus replication in infected cells. Studies with blocking monoclonal antibodies against B7-1 or B7-2

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28

PAGOU, Margarita, and Antonios KOUTSELINIS. "Lipophilicity and Chromatographic Behaviour of Benzoic Acid Derivatives." CHEMICAL & PHARMACEUTICAL BULLETIN 41, no. 2 (1993): 319–24. http://dx.doi.org/10.1248/cpb.41.319.

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29

Cabanillas, Billy, Anne-Cécile Le Lamer, Denis Castillo, et al. "Dihydrochalcones and Benzoic Acid Derivatives from Piper dennisii." Planta Medica 78, no. 09 (2012): 914–18. http://dx.doi.org/10.1055/s-0031-1298459.

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30

Chen, Yi-Pei, Chad C. Catbagan, Jeannette T. Bowler, et al. "Evaluation of benzoic acid derivatives as sirtuin inhibitors." Bioorganic & Medicinal Chemistry Letters 24, no. 1 (2014): 349–52. http://dx.doi.org/10.1016/j.bmcl.2013.11.004.

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31

Chitiva-Chitiva, Luis C., Cristóbal Ladino-Vargas, Luis E. Cuca-Suárez, Juliet A. Prieto-Rodríguez, and Oscar J. Patiño-Ladino. "Antifungal Activity of Chemical Constituents from Piper pesaresanum C. DC. and Derivatives against Phytopathogen Fungi of Cocoa." Molecules 26, no. 11 (2021): 3256. http://dx.doi.org/10.3390/molecules26113256.

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In this study, the antifungal potential of chemical constituents from Piper pesaresanum and some synthesized derivatives was determined against three phytopathogenic fungi associated with the cocoa crop. The methodology included the phytochemical study on the aerial part of P. pesaresanum, the synthesis of some derivatives and the evaluation of the antifungal activity against the fungi Moniliophthora roreri, Fusarium solani and Phytophthora sp. The chemical study allowed the isolation of three benzoic acid derivatives (1–3), one dihydrochalcone (4) and a mixture of sterols (5–7). Seven derivat

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32

George, Roy. "Adsorption Equilibrium and Kinetic Studies of Effect of ortho-Substitution to Benzoic Acid in Aqueous Phase Using Granular Activated Carbon." Asian Journal of Chemistry 31, no. 8 (2019): 1667–74. http://dx.doi.org/10.14233/ajchem.2019.21938.

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Adsorption equilibrium and kinetics studies of effect of ortho-substituted benzoic acid in aqueous phase using granular activated carbon were investigated. The granular activated carbon (GAC) obtained from bituminous type coal having a surface area of 998 m2/g and loosely bounded and open pores morphology. The adorbates selected for this study was benzoic acid and its ortho-derivatives namely; salicylic acid, phthalic acid and o-toluic acid. The solubility of adsorbate in solvent affected the adsorption behaviour more pronouncly. The order of adsorption for adsorbates was found to be as: benzo

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33

Journal, Baghdad Science. "Synthesis of New Heterocyclic Derivatives from 4-(3, 5-Dimethyl-1-phenyl-1H-pyrazol-4-ylazo)- benzoic acid." Baghdad Science Journal 7, no. 1 (2010): 727–36. http://dx.doi.org/10.21123/bsj.7.1.727-736.

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In this work pyrazolin derivatives were prepared from the diazonium chloride salt of 4-aminobenzoic acid. Azo compounds were prepared from the reaction of an ethanolic solution of sodium acetate and calculated amount of active methylene compound namely, acetyl acetone to obtain the corresponding hydrazono derivative (1). Cyclocondensation reaction of compounds (1) with hydrazine hydrate and phenyl hydrazine in boiling ethanol affording the corresponding pyrazoline-5-one derivatives of 4-aminobenzoic acid (2,3). Then compound (3) was reacted with thionyl chloride to give the corresponding acid

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34

Begini, Francesca, Dorota Krasowska, Aleksandra Jasiak, Jozef Drabowicz, Claudio Santi, and Luca Sancineto. "Continuous flow synthesis of 2,2′-diselenobis(benzoic acid) and derivatives." Reaction Chemistry & Engineering 5, no. 4 (2020): 641–44. http://dx.doi.org/10.1039/d0re00012d.

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35

Kettle, A. J., C. A. Gedye, M. B. Hampton, and C. C. Winterbourn. "Inhibition of myeloperoxidase by benzoic acid hydrazides." Biochemical Journal 308, no. 2 (1995): 559–63. http://dx.doi.org/10.1042/bj3080559.

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Myeloperoxidase is the most abundant protein in neutrophils and catalyses the conversion of H2O2 and chloride into HOCl. To help clarify the role of this enzyme in bacterial killing and inflammation, a specific and potent inhibitor needs to be identified. We have studied a series of benzoic acid hydrazides and found that in general they inhibit the peroxidation activity of myeloperoxidase with an IC50 value of less than 10 microM. The IC50 values of derivatives with substituents containing oxygen or nitrogen were related to their Hammett substituent constants. This indicates that myeloperoxida

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36

Dileep, K. V., C. Remya, J. Cerezo, A. Fassihi, H. Pérez-Sánchez, and C. Sadasivan. "Comparative studies on the inhibitory activities of selected benzoic acid derivatives against secretory phospholipase A2, a key enzyme involved in the inflammatory pathway." Molecular BioSystems 11, no. 7 (2015): 1973–79. http://dx.doi.org/10.1039/c5mb00073d.

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37

Velika, Beata, and Ivan Kron. "Antioxidant properties of benzoic acid derivatives against Superoxide radical." Free Radicals and Antioxidants 2, no. 4 (2012): 62–67. http://dx.doi.org/10.5530/ax.2012.4.11.

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38

Sánchez de la ßlanca, E., J. L. Núñez, and P. Martínez. "Vibrational spectra of some o-substituted benzoic acid derivatives." Journal of Molecular Structure 142 (March 1986): 45–48. http://dx.doi.org/10.1016/0022-2860(86)85059-1.

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39

TERREAUX, C., M. P. GUPTA, and K. HOSTETTMANN. "ChemInform Abstract: Antifungal Benzoic Acid Derivatives from Piper Dilatatum." ChemInform 30, no. 2 (2010): no. http://dx.doi.org/10.1002/chin.199902259.

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40

Nishikawa, Etsushi, Jun Yamamoto, and Hiroshi Yokoyama. "Synthesis and Properties of Perfluoroalkylalkoxy Substituted Benzoic Acid Derivatives." Chemistry Letters 30, no. 2 (2001): 94–95. http://dx.doi.org/10.1246/cl.2001.94.

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41

Lago, João Henrique G., Clécio Sousa Ramos, Diego Campos C. Casanova, et al. "Benzoic Acid Derivatives fromPiperSpecies and Their Fungitoxic Activity againstCladosporiumcladosporioidesandC.sphaerospermum." Journal of Natural Products 67, no. 11 (2004): 1783–88. http://dx.doi.org/10.1021/np030530j.

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42

Orjala, J., C. Erdelmeier, A. Wright, B. Baumgartner, T. Rali, and O. Sticher. "Biologically Active Phenylpropene and Benzoic Acid Derivatives fromPiper aduncumLeaves." Planta Medica 55, no. 07 (1989): 619–20. http://dx.doi.org/10.1055/s-2006-962176.

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43

Bai, Binglian, Haitao Wang, Hong Xin, Beihong Long, and Min Li. "Liquid crystalline behaviour of benzoic acid derivatives containing alkoxyazobenzene." Liquid Crystals 34, no. 6 (2007): 659–65. http://dx.doi.org/10.1080/02678290701328118.

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44

Abraham, Wolf-Rainer, and Hans-Adolf Arfmann. "Hydroxy-(methylbutenynyl)-benzoic acid and derivatives from Curvularia fallax." Phytochemistry 29, no. 8 (1990): 2641–44. http://dx.doi.org/10.1016/0031-9422(90)85203-r.

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45

Correa-Basurto, José, Judith Espinosa-Raya, Iván Vázquez-Alcántara, Cesar A. Flores-Sandoval, and José Trujillo-Ferrara. "(10) Ex vivo anticholinesterase activity of benzoic acid derivatives." Chemico-Biological Interactions 157-158 (December 2005): 368–69. http://dx.doi.org/10.1016/j.cbi.2005.10.055.

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46

Láznícek, M. "P178 pharmacokinetics of some benzoic acid derivatives in rats." European Journal of Pharmaceutical Sciences 2, no. 1-2 (1994): 163. http://dx.doi.org/10.1016/0928-0987(94)90351-4.

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47

Tolstorozhev, G. B., M. V. Bel′kov, I. V. Skornyakov, et al. "Infrared Spectroscopy of Hydrogen Bonds in Benzoic Acid Derivatives." Journal of Applied Spectroscopy 81, no. 1 (2014): 109–17. http://dx.doi.org/10.1007/s10812-014-9895-8.

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48

Akbas, Esvet, Ela Yildiz, and Ahmet Erdogan. "Synthesis, characterization and theoretical studies of novel pyrimidine derivatives as potential corrosion inhibitors." Journal of the Serbian Chemical Society 85, no. 4 (2020): 481–92. http://dx.doi.org/10.2298/jsc190326081a.

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In this study, five new pyrimidine derivatives were synthesized and characterized by characterization methods such as 1H-NMR, 13C-NMR, FT- -IR and elemental analysis. The corrosion inhibition activity of the synthesized compounds was examined by theoretical calculation using DFT method at the level of B3LYP/6-31G (d,p). According to the calculations, 4-(6-benzoyl-2- -benzylidene-3-oxo-7-phenyl-2,3-dihydro-5H-thiazolo[3,2-a]pyrimidin-5-yl)- benzoic acid (6) appears to be a good inhibitor for corrosion.

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Barrientos, Ruth E., Mario J. Simirgiotis, Javier Palacios, et al. "Chemical Fingerprinting, Isolation and Characterization of Polyphenol Compounds from Heliotropium taltalense (Phil.) I.M. Johnst and Its Endothelium-Dependent Vascular Relaxation Effect in Rat Aorta." Molecules 25, no. 14 (2020): 3105. http://dx.doi.org/10.3390/molecules25143105.

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Heliotropium taltalense is an endemic species of the northern coast of Chile and is used as folk medicine. The polyphenolic composition of the methanolic and aqueous extract of the endemic Chilean species was investigated using Ultrahigh-Performance Liquid Chromatography, Heated Electrospray Ionization and Mass Spectrometry (UHPLC-Orbitrap-HESI-MS). Fifty-three compounds were detected, mainly derivatives of benzoic acid, flavonoids, and some phenolic acids. Furthermore, five major compounds were isolated by column chromatography from the extract, including four flavonoids and one geranyl benzo

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Kuchař, Miroslav, Bohumila Brunová, Richard Junek, et al. "The Antileukotrienic Derivatives and Homologues of [(Quinolin-2-ylmethoxy)sulfanyl]benzoic Acids with Reduced Lipophilicity." Collection of Czechoslovak Chemical Communications 70, no. 9 (2005): 1357–71. http://dx.doi.org/10.1135/cccc20051357.

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A series of ({[(quinolin-2-ylmethoxy)phenyl]sulfanyl}phenyl)acetic acids 2 and S-oxidized derivatives of {[(quinolin-2-ylmethoxy)phenyl]sulfanyl}benzoic acids 3 were prepared and their antileukotrienic and antiasthmatic activities evaluated. Regression analysis led to the conclusion that the antileukotrienic activities of compounds 2 correspond to the relationships between these activities and lipophilicity, derived for the previously synthesized series of substituted (arylsulfanyl)benzoic acids 1A, 1B and 1C. Acids 3 are outliers from these relationships, probably due to a somewhat different

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