Relevant bibliographies by topics / Benzoic acid derivatives

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Benzoic acid derivatives'

Author: Grafiati
Published: 4 June 2021
Last updated: 11 February 2022

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Journal articles on the topic "Benzoic acid derivatives"

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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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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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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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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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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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., 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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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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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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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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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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Dissertations / Theses on the topic "Benzoic acid derivatives"

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Cavalcanti, Élida Batista Vieira Sousa. "Estudo fitoquímico e biológico dos frutos e raízes de Piper caldense C. DC. (Piperaceae)." Universidade Federal da Paraíba, 2014. http://tede.biblioteca.ufpb.br:8080/handle/tede/8057.

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Submitted by Clebson Anjos (clebson.leandro54@gmail.com) on 2016-03-29T19:16:04Z No. of bitstreams: 1 arquivototal.pdf: 5534324 bytes, checksum: 898113655c311035d0ba3661db9223c8 (MD5)<br>Made available in DSpace on 2016-03-29T19:16:04Z (GMT). No. of bitstreams: 1 arquivototal.pdf: 5534324 bytes, checksum: 898113655c311035d0ba3661db9223c8 (MD5) Previous issue date: 2014-02-27<br>Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPq<br>The genus Piper L. is the largest one among the Piperaceae. Containing at least 1000 species, they are located mainly on the neotr
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Silva, Gracielle Angeline Tavares da. "Estudo fitoquímico das folhas e frutos de Piper caldense C.DC. (Piperaceae)." Universidade Federal da Paraí­ba, 2013. http://tede.biblioteca.ufpb.br:8080/handle/tede/6799.

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Made available in DSpace on 2015-05-14T12:59:56Z (GMT). No. of bitstreams: 1 arquivototal.pdf: 8420094 bytes, checksum: e38d9fce0fc67703d2f3e878474b7c32 (MD5) Previous issue date: 2013-02-27<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES<br>The Piper L. genus is the largest one among the Piperaceae. Containing at least 1000 species, they are located mainly on the neotropical region of Earth and it draws our attention due to its medical, economical, chemical and cultural properties, such as anti-inflamatory, antibacterial and fungicide actions. Piper genus species ha
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Salim, Sachithananthan Sharlinda Binti. "Studies of local structure and nucleation in benzoic acid derivative systems." Thesis, University of Leeds, 2017. http://etheses.whiterose.ac.uk/18780/.

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Nucleation of organic crystals from solution starts from self-assembly of molecules. New and advanced techniques are continuously explored to have an insight into understanding the nucleation mechanism and the local structure in both solution and resulting crystalline forms. In this thesis, multiple spectroscopic techniques were applied - infrared (IR), Raman, near-edge X-ray absorption fine structure (NEXAFS) and X-ray photoelectron (XPS) - that gave an extensive overview of local interactions between molecules. The nucleation rates were calculated based on probability distributions of induct
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Eyrich, Berit. "Untersuchungen zur Biotransformation neuer substituierter Piperidylbenzilate." Doctoral thesis, [S.l.] : [s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=964723913.

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Smolinka, Kai. "Biomimetische Studien an Arzneistoffen mit Benzilsäure- oder Estrogenstruktur." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2001. http://dx.doi.org/10.18452/14638.

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In der vorliegenden Arbeit wurden chemische Modellsysteme zur Erarbeitung möglicher Metabolisierungswege für neue, als potentielle Antiparkinsonmittel entwickelte Benzilsäurederivate angewendet und die Anwendbarkeit solcher Systeme zur Modellierung der Biotransformation von Estrogenderivaten getestet. Die biomimetischen Umsetzungen wurden im wässrigen und nichtwässrigen Milieu mit Mangan- und Eisenporphyrinen als Katalysatoren, mit einer Stickstoffbase, in der Regel Imidazol, als Co-Katalysator und mit Wasserstoffperoxid, Iodosylbenzen oder tert-Butylhydroperoxid als Sauerstoffquelle durchge
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Selent, Jana. "Darstellung und Charakterisierung neuartiger, chiraler, basischer Benzilsäureester mit anticholinerger Wirkung." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2005. http://dx.doi.org/10.18452/15166.

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Basische Benzilsäureester stellen mit ihrer ausgeprägten anticholinergen Wirksamkeit potenzielle Arzneistoffe zur Behandlung der Harninkontinenz, der Ulkuserkrankung und des Morbus Parkinson dar. Von besonderem Interesse sind Benzilsäurevertreter, die neben anticholinergen auch dopaminerge Effekte aufweisen. Wegen ihrer dualistischen Wirkung könnten sie eine neue Klasse von Antiparkinsonica begründen. Aufgrund der vielfältigen Funktionen von Muscarinrezeptoren treten bei wenig selektiv wirksamen Arzneistoffen atropinartige Nebenwirkungen auf. Mit der Entwicklung von Verbindungen, die eine erhö
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Shu-Wei, Hsu, and 許書維. "Synthesis and Biological Activities of 2-Substituted Benzyloxy Benzoic Acid Derivatives." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/48608478932630792656.

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碩士<br>中國醫藥學院<br>藥物化學研究所<br>91<br>In order to obtain novel compounds with potent anti-inflammatory, anti-allergic and anti-diarrhea activities, 2-benzyloxybenzaldehyde was used as the lead compound, and 2-substituted benzyloxy benzoic acid derivatives were synthesized. 2-substituted benzyloxy benzonitriles 17-25, 2-substituted benzyloxy 2-methylbenzenes 26-29, 2-substituted benzyloxy phenyl methanols 30-33, 2-substituted benzyloxy benzoates 34-41, 2-substituted benzyloxy benzamides 42-44 and 2-substituted benzylamino benzoates 45-55 were synthesized by the benzylation with potassium
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Lin, Shih-Chieh, and 林仕杰. "Synthesis and study on self-assembled nanostructures of bisphenol F derivatives base on 4-(alkoxy)benzoic acid and 3,4-bis(alkoxy)benzoic acid." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/83938674229993765662.

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碩士<br>國立高雄師範大學<br>化學系<br>100<br>A series of bis(4-n-alkyloxy) monobenzoylglyceride) bisphenol F were synthesized. Further reaction by heating in neat condition induces a 3,2-acyl migration which determined by 1-D and 2-D NMR spectrum.The ratio of the structural isomer is able to modulate the fluorescence and morphology of the blended system, and we dementrated that the phenomenon is due to formation of the different type of the intermolecular hydrogen bonding species in each series. In the experimental results, all the compounds show layer structure in solid at low temperature and Pm3n liquid
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Chin-Wen, Wang, and 王志文. "Synthesis of 2-(benzyloxy)benzoic acid derivatives as the inhibitor of ganglioside GM1 receptor." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/38257738085262709567.

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碩士<br>中國醫藥大學<br>藥物化學研究所<br>93<br>Structural biology studies on heat-labile enterotoxin (LT) from enterotoxigenic Escherichia coli. and the closely related cholera toxin (CT), shed light on the action mechanism of toxin at molecular and atomic levels. The B pentamer protein of the toxins recognized the receptor ganglioside GM1 presented on the gastrointestinal tract of human host and triggers endocytosis . The enzymatic A1 fragment of the toxin enters the cytosol it modifies the alpha subunit of stimulatory G protein (Gsα) and locks the G protein in its GTP-bound form, which continually stimula
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Lu, Hsiu-Yu, and 呂秀玉. "Reduction Reactions of Benzoic Acid and Zinc Porphyrin Derivatives in Tetrahydrofuran: An Electrochemical Study." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/77264628226750664161.

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碩士<br>國立暨南國際大學<br>應用化學系<br>100<br>In this thesis, we study reduction reactions of benzoic acid and zinc porphyrin derivatives in tetrahydrofuran. By adding H2O in tetrahydrofuran, we observed positive shift of the reduction potentials. In addition, we studied the influence of the long alkyl chains and electron-donating or withdrawing substituent on the reduction potentials of the carboxylic acid. As for the potentiostatic coulometry, we studied acid reductions by fixing the potentials upon electrolysis. However, we found no evidence of continuous hydrogen generation. The UV-visible absorption
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Book chapters on the topic "Benzoic acid derivatives"

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Uknes, Scott, Shericca Morris, Bernard Vernooij, and John Ryals. "The Role of Benzoic Acid Derivatives in Systemic Acquired Resistance." In Phytochemical Diversity and Redundancy in Ecological Interactions. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-1754-6_10.

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Griesbeck, A. G. "Using Benzoic Acid Derivatives." In Quinones and Heteroatom Analogues. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-028-00631.

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Kikelj, D. "From 2-(Acylamino)benzoic Acid Derivatives and Ammonia." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00776.

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Taber, Douglass F. "Benzene Derivatives: The Tanino-Miyashita Synthesis of Zoanthenol." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0061.

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Yuqing Hou of Southern Illinois University found (J. Org. Chem. 2009, 74, 6362) that the peroxy ether 2 served effectively to directly transfer a methoxy group to the lithiated 1 to give 3. Wanzhi Chen of Zhejiang University, Xixi Campus, showed (J. Org. Chem. 2009, 74, 7203) that pyrimidines such as 4, readily prepared from the corresponding phenol, underwent smooth Pd-catalyzed ortho acetoxylation. Trond Vidar Hansen of the University of Oslo observed (Tetrahedron Lett. 2009, 50, 6339) that simple electrophilic formylation of phenols such as 6 also proceeded with high ortho selectivity. Kyung Woon Jung of the University of Southern California optimized (J. Org. Chem. 2009, 74, 6231) the Rh catalyst for ortho C-H insertion, converting 8 into 9. Jin-Quan Yu of Scripps/La Jolla devised (Science 2010, 327, 315) a protocol for carboxy-directed catalytic ortho palladation that allowed subsequent Heck coupling, transforming 10 into 11. Norikazu Miyoshi of the University of Tokushima established (Chem. Lett. 2009, 38, 996) that in situ generated strontium alkyls added 1,6 to benzoic acid 13, to give, after mild oxidative workup, the 4-alkyl benzoic acid 15. Amin Zarei of Islamic Azad University showed (Tetrahedron Lett. 2009, 50, 4443) that their previously developed protocol for preparing stable diazonium silica sulfates could be extended to the preparation of an aryl azide such as 17. Stephen L. Buchwald of MIT developed (J. Am. Chem. Soc. 2009, 131, 12898) a Pd-mediated protocol for the conversion of aryl chlorides to the corresponding nitro aromatics. Virgil Percec of the University of Pennsylvania has also reported (Organic Lett. 2009, 11, 4974) the conversion of an aryl chloride to the borane, and Guy C. Lloyd-Jones has described (Angew. Chem. Int. Ed. 2009, 48, 7612) the conversion of phenols to the corresponding thiols. Kwang Ho Song of Korea University and Sunwoo Lee of Chonnam National University demonstrated (J. Org. Chem. 2009, 74, 6358) that the Ni-mediated homologation of aryl halides worked with a variety of primary and secondary formamides. Kwangyong Park of Chung-Ang University observed (J. Org. Chem. 2009, 74, 9566) that Ni catalysts also mediated the coupling of Grignard reagents with the tosylate 22 not in the usual way but with the C-S bond to give 23.
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Hlaváč, Jan, Pavel Hradil, Miroslav Soural, and Lucie Spáčilová. "Use of Phenacylesters of Substituted Benzoic Acid for Synthesis of Derivatives of 2-Phenyl-3-Hydroxy-4(1H)-Quinolones." In 19th International Congress on Heterocyclic Chemistry. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50168-4.

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Chen, S., E. C. Salo, and N. J. Kerrigan. "Benzo-1,2-quinone Derivatives." In Lewis Base and Acid Catalysts. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-204-00231.

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Kollenz, G. "Reaction of Di--butoxyacetylene with Benzoyl Isocyanate." In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00355.

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Kollenz, G., and S. Ebner. "Thermolysis of 4-Benzoyl-5-phenylfuran-2,3-dione." In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00283.

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Kollenz, G., and S. Ebner. "Flash-Vacuum Pyrolysis of 4-Benzoyl-5-phenylfuran-2,3-dione." In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00282.

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Barton, Derek H. R., Michael Bolton, Philip D. Magnus, and Peter J. West. "Photochemical Transformations.: Part XXXIII. Photolysis of Thio-benzoic Acid O-Esters. Part IV. Photolysis of O-Phenethyl Thiobenzo-ate Derivatives and the Formation of Thioketones." In World Scientific Series in 20th Century Chemistry. WORLD SCIENTIFIC / IMPERIAL COLLEGE PRESS, 1996. http://dx.doi.org/10.1142/9789812795984_0055.

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Conference papers on the topic "Benzoic acid derivatives"

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Yildiz, Melike, Deryanur Kiliç, Yağmur Ünver, Murat Şentürk, Hakan Askin, and Ömer İrfan Küfrevioğlu. "Acetylcholinesterase inhibitory properties of some benzoic acid derivatives." In INTERNATIONAL CONFERENCE ON ADVANCES IN NATURAL AND APPLIED SCIENCES: ICANAS 2016. Author(s), 2016. http://dx.doi.org/10.1063/1.4945928.

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Bialecka-Florjanczyk, Ewa, and Irma Sledzinska. "Mesogenic 4-substituted benzoic acid derivatives with oxyethylene chains." In XIV Conference on Liquid Crystals, Chemistry, Physics, and Applications, edited by Jolanta Rutkowska, Stanislaw J. Klosowicz, and Jerzy Zielinski. SPIE, 2002. http://dx.doi.org/10.1117/12.472177.

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Lu, Rong, Hai-xia Ma, Wei-ping Liu, and Wen-xin Li. "Studies on quantitative structure-activity-relationship inhibitory effects of benzoic acid derivatives on tyrosinase." In 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE 2010). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5516550.

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Kiliç, Deryanur, Melike Yildiz, Murat Şentürk, Orhan Erdoğan, and Ömer İrfan Küfrevioğlu. "Comparison of inhibition effects of some benzoic acid derivatives on sheep heart carbonic anhydrase." In INTERNATIONAL CONFERENCE ON ADVANCES IN NATURAL AND APPLIED SCIENCES: ICANAS 2016. Author(s), 2016. http://dx.doi.org/10.1063/1.4945922.

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Georgousaki, K., N. Tsafantakis, S. Gumeni, et al. "Bjerkandera adusta as a source of benzoic acid derivatives targeting 26S proteasome and cathepsins B&L." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399861.

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Nadaf, Y. F. "OLED display application of 2-(6-Fluoro-2-oxo-2H-chromen-4-ylmethoxy)-benzoic acid methyl ester derivative." In PROF. DINESH VARSHNEY MEMORIAL NATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF MATERIALS: NCPCM 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5098660.

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