Relevant bibliographies by topics / Amide cinnamic acid derivatives

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Amide cinnamic acid derivatives'

Author: Grafiati
Published: 24 April 2022
Last updated: 30 July 2025

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Journal articles on the topic "Amide cinnamic acid derivatives"

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Todorova, Daniela, Maria Tupova, Veneta Zapreva, Tsenka Milkova, and Atanas Kujumdjiev. "Transformation of Aminosteroids into Pharmacologically Active Amides of Phenolic Acids." Zeitschrift für Naturforschung C 54, no. 1-2 (1999): 65–69. http://dx.doi.org/10.1515/znc-1999-1-212.

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Amides of cinnamic acid derivatives with 3α-and 3β-cholestanylamines, as well as with 3α-and 3β-amino-(2’-aminoethyl)-cholest-5-en were synthesized using dicyclohexylcarbodiimide (DCC) and 1-hydroxy-benzotriazole as efficient additives. Their structure was determined by UV and 1HNMR . 3β-Amino-(2’-aminoethyl)-cholest-5-en, amides of p-hydroxy-cinnamic acid 4 and 9, and N-cholest-5-en-3α-aminoethyl-di-(3’’,-phenyl-trans-2’’-propene)-amide 10 showed moderate antibacterial activity against Staphylococcus aureus
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Nimse, Satish Balasaheb, Dilipkumar Pal, Avijit Mazumder, and Rupa Mazumder. "Synthesis of Cinnamanilide Derivatives and Their Antioxidant and Antimicrobial Activity." Journal of Chemistry 2015 (2015): 1–5. http://dx.doi.org/10.1155/2015/208910.

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The amide derivatives of cinnamic acid were synthesized and their antimicrobial and antioxidant activities were investigated. The investigation of antimicrobial potentials of the compounds demonstrated a strong activity against 21 bacterial strains comprising Gram-positive and Gram-negative bacteria. Compounds2a,2b, and3bshowed strong antimicrobial activity against all microorganisms with the pMIC value ranging from 2.45 to 3.68. Compounds2a,3a, and3bdemonstrated strong antioxidant activity with % inhibition of the DPPH radical of 51% (±1.14), 41% (±1.01), and 50% (±1.23), respectively. These
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Geetika, Vaisnav, K. Chakraborty Anup, and Karole Sarita. "Design, synthesis and evaluation of some novel derivatives of cinnamic acid as anti-inflammatory agents." World Journal of Biology Pharmacy and Health Sciences 14, no. 1 (2023): 088–96. https://doi.org/10.5281/zenodo.8037041.

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The role of Cinnamic acid derivatives as antioxidants, antimicrobial agents, antidiabetic drugs, anticancer drugs etc. is well reported. A thorough literature search revealed that the substitution on carboxylic acid group of Cinnamic acids by different amines imparts the potent conjugates. The quest for the design of effective anti-inflammatory drugs is still the primal focus of several research works world-wide owing to the side effects associated with the existing drugs. The side effects of the existing drugs are associated with the presence of the free carboxyl group in the molecules. In th
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Geetika Vaisnav, Anup K Chakraborty, and Sarita Karole. "Design, synthesis and evaluation of some novel derivatives of cinnamic acid as anti-inflammatory agents." World Journal of Biology Pharmacy and Health Sciences 14, no. 1 (2023): 088–96. http://dx.doi.org/10.30574/wjbphs.2023.14.1.0164.

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The role of Cinnamic acid derivatives as antioxidants, antimicrobial agents, antidiabetic drugs, anticancer drugs etc. is well reported. A thorough literature search revealed that the substitution on carboxylic acid group of Cinnamic acids by different amines imparts the potent conjugates. The quest for the design of effective anti-inflammatory drugs is still the primal focus of several research works world-wide owing to the side effects associated with the existing drugs. The side effects of the existing drugs are associated with the presence of the free carboxyl group in the molecules. In th
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Rasyid, Herlina, Teni Ernawati, and Indah Muthmainnah Monoarfa. "2-Cinnamamido-4-Methylpentanamide and N-(2-Hydroxypropanoyl)Cinnamamide: Synthesis, Characterization, and Molecular Docking Studies Through PBP2a Protein." Molekul 19, no. 2 (2024): 262. http://dx.doi.org/10.20884/1.jm.2024.19.2.10154.

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ABSTRACT. Cinnamic acid has been found in several types of plants and has a diverse spectrum of bioactivity. Derivatization of cinnamic acid related to the improving bioactivity of a compound. Cinnamic acid can be found as an acid or in conjugated form with amides, esters, aldehydes. This research focus on the synthesis of amide derivatives of cinnamic acid to improve the bioactivity. Two compounds namely 2-cinnamamido-4-methylpentanamide (1a) and N-(2-hydroxypropanoyl)cinnamamide (1b) were carried out through amidation reaction using carbodiimide coupling reagent for 24 hours. The synthesized
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Fotopoulos, Ioannis, Eleni Pontiki, and Dimitra Hadjipavlou Litina. "Targeting Inflammation with Conjugated Cinnamic Amides, Ethers and Esters." Letters in Drug Design & Discovery 17, no. 1 (2019): 3–11. http://dx.doi.org/10.2174/1570180816666181129125511.

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Background: Cinnamic acid is a key intermediate in shikimate and phenylpropanoid pathways. It is found both in free form, and especially in the form of esters in various essential oils, resins and balsams which are very important intermediates in the biosynthetic pathway of several natural products. The cinnamic derivatives play a vital role in the formation of commercially important intermediate molecules which are necessary for the production of different bioactive compounds and drugs. Different substitutions on basic moiety lead to various biological activities. Furthermore, combination of
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Kabat, Małgorzata, Justyna Popiół, and Agnieszka Gunia-Krzyżak. "Cinnamic Acid Derivatives as Potential Multifunctional Agents in Cosmetic Formulations Used for Supporting the Treatment of Selected Dermatoses." Molecules 29, no. 23 (2024): 5806. https://doi.org/10.3390/molecules29235806.

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Cinnamic acid and its natural derivatives were primarily used in cosmetics as fragrance materials as well as skin and hair conditioners. Nowadays, not only natural but also synthetic cinnamic acid derivatives are used as active ingredients of cosmetic formulations. They still serve as fragrance ingredients but also as active ingredients supporting the treatment of selected dermatoses such as acne vulgaris, atopic dermatitis, and hyperpigmentation. They are also commonly used in anti-aging cosmetic formulations. On the other hand, several cinnamic acid derivatives used as fragrances in cosmetic
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Menezes, José C. J. M. D. S., and Vinícius R. Campos. "Bench to Any Side—The Pharmacology and Applications of Natural and Synthetic Alkylated Hydroxy Cinnamates and Cinnamides." Compounds 4, no. 4 (2024): 729–76. https://doi.org/10.3390/compounds4040044.

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Natural alkylated hydroxy cinnamates (AHCs) isolated from medicinal plants and the thereby designed and synthesized cinnamides are derivatives of hydroxy cinnamic acids such as p-coumaric, sinapic, ferulic, and caffeic acids, which are naturally derived from human dietary sources. The pharmacological properties displayed by AHCs based on their inherent structure range include antioxidant, antimicrobial, antiplasmodial, anti-tyrosinase, Alzheimer’s and Parkinson’s disease therapy, anticancer therapy, metabolic disease therapy, and biopesticides, which have not been reviewed together. Based on t
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Gür, Zehra Tuğçe, Fatma Sezer Şenol, Suhaib Shekfeh, İlkay Erdoğan Orhan, Erden Banoğlu, and Burcu Çalişkan. "Novel Piperazine Amides of Cinnamic Acid Derivatives as Tyrosinase Inhibitors." Letters in Drug Design & Discovery 16, no. 1 (2018): 36–44. http://dx.doi.org/10.2174/1570180815666180420105652.

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Background: A series of novel cinnamic acid piperazine amide derivatives has been designed and synthesized, and their biological activities were also evaluated as potential tyrosinase inhibitors. Methods: Compounds 9, 11 and 17 showed the most potent biological activity (IC50 = 66.5, 61.1 and 66 µM, respectively). In silico docking simulation was performed to position compound 11 into the Agaricus bisporus mushroom tyrosinase’s active site to determine the putative binding interactions. Results and Conclusion: The results indicated that compound 11 could serve as a promising lead comp
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Pangaribowo, Dian Agung, Fathunnisa Fathunnisa, Ari Satia Nugraha, Ayik Rosita Puspaningtyas, and Indah Purnama Sary. "Structure Modification of Cinnamic Acid to (E)-1-(3,4-dihydroisoquinoline-2(1H)-yl)-3-phenylprop-2-en-1-one and Antioxidant Activity Test by DPPH Method." Borneo Journal of Pharmacy 7, no. 3 (2024): 254–63. http://dx.doi.org/10.33084/bjop.v7i3.6163.

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Antioxidants can protect cells from free radical damage by stabilizing them. One of the compounds that has antioxidant activity is cinnamic acid. Cinnamic acid and its derivatives have several activities: antibacterial, anticancer, and antioxidant. However, the ability of cinnamic acid to capture free radicals is still relatively low. One of the efforts that can be made to increase the antioxidant activity of cinnamic acid is to modify its structure. Structure modification is an effort to improve the pharmacological activity of a compound through chemical synthesis reactions. The cinnamic acid
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Dissertations / Theses on the topic "Amide cinnamic acid derivatives"

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McNichols, Brett William. "Synthesis and Application of Styryl Phosphonic and Cinnamic Acid Derivatives." Thesis, Colorado School of Mines, 2017. http://pqdtopen.proquest.com/#viewpdf?dispub=10624231.

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<p> Styryl phosphonic and cinnamic acid derivatives have been gaining attention as key candidates to modulate specific electrode properties in organic electronic devices such as work function, surface energies, wettability, and electron charge transfer kinetics that lead to increased efficiency, operational range, and device lifetimes. Very few of these acids are commercially available. The driving factor behind this research is to explore simple, high yield, and inexpensive synthetic routes towards synthesis of these acids. Herein, the novel synthesis of vinyl phosphonic acids (VPAs) and thei
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Nguyen, Dao. "SYNTHESIS OF A NOVEL FAMILY OF AMIDE DERIVATIVES OF PODOCARPIC ACID." Master's thesis, University of Central Florida, 2004. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/2221.

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As a class, amides are of great interest in biological studies and pharmaceutical application. In this work, podocarpic acid, a natural tricyclic diterpene, derived from Podocarpus species, has been employed to form a novel family of amide derivatives which will later be studied for their potential as new drug leads. Novel amide derivatives of podocarpic acid were synthesized from podocarpic acid in three steps. The first step involved methylation with dimethylsulfate to form methyl-O-methylpodocarpate. This step was followed by iodination with iodine to give iodomethyl-O-methylpodocarpate. Fi
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Koch, Horst, André Laschewsky, Helmut Ringsdorf, and Kang Teng. "Photodimerization and photopolymerization of amphiphilic cinnamic acid derivatives in oriented monolayers, vesicles and solution." Universität Potsdam, 1986. http://opus.kobv.de/ubp/volltexte/2008/1711/.

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Cinnamic acid moieties were incorporated into amphiphilic compounds containing one and two alkyl chains. These lipid-like compounds with photoreactive units undergo self-organization to form monolayers at the gas-water interface and bilayer structures (vesicles) in aqueous solutions. The photoreaction of the cinnamic acid moiety induced by 254 nm UV light was investigated in the crystalline state, in monolayers, in vesicles and in solution in organic solvents. The single-chain amphiphiles undergo dimerization to yield photoproducts with twice the molecular weight of the corresponding monomers
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Gregar, Travis Quinton. "Synthesis and structural characterization of amide-linked derivatives of N-acetyl neuraminic acid." Diss., The University of Arizona, 2001. http://hdl.handle.net/10150/279827.

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Amide linked carbohydrates represent a tremendously different type of compound. Sugars have traditionally been linked together as either N or O linked via the anomeric carbon to make larger compounds, i.e. Sialyl Lewis X. This linkage leads to great instability under acidic and biological conditions. N-Acetyl neuraminic acid is a naturally occurring delta peptide. Colominic acid is the naturally occurring O linked polymer of N-acetyl neuraminic acid. This polymer has been found to possess a helical structure starting at the hexamer length. Changing from an O linkage to an amide linkage provid
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Theddu, Naresh. "APPLICATIONS OF ENANTIOPURE SULFINIMINE DERIVED CHIRAL AMINE BUILDING BLOCKS FOR THE ASYMMETRIC SYNTHESIS OF TROPANE ALKALOIDS AND CYCLIC CIS BETA-AMINO ACID DERIVATIVES." Diss., Temple University Libraries, 2011. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/157444.

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Chemistry<br>Ph.D.<br>Chiral amines are ubiquitous in natural products and are found in many drugs and drug candidates. Enantiopure sulfinimines [RS(O)N=CHR1] are useful chiral building blocks for the stereoselective synthesis of amines and amine derivatives. The aim of this thesis research is to develop new methods to access chiral amine building blocks for applications in the synthesis of nitrogen-heterocycles including ring-substituted tropinones, tropanes, cyclic cis-beta-amino acid derivatives, and amino-cyclopentitols.<br>Temple University--Theses
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fadhil, ali abd al-karim alkarim. "Reversed-phase and surfactant modified reversed-phase high and ultra-high performance liquid chromatography of phenolic and aliphatic carboxylic acids." Miami University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=miami1574428923192499.

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Leblanc, Jean-Pierre. "Synthese et caracterisation de polycondensats renfermant des motifs stilbeniques." Paris 6, 1988. http://www.theses.fr/1988PA066350.

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Polycondensation de l'acide trans stilbenedicarboxylique-4,4' (soa) avec des alpha ,omega -diamino alcanes et des alpha ,omega -diamino oligoethers. Etude de l'incorporation du soa dans des copolyarylates comme le poly(isophtalate de methyl phenylene) en vue d'obtenir des polymeres cristaux liquides, et des polyesters obtenus a partir d'autres monomeres (acide terephtalique). Amelioration des proprietes mecaniques des polycondensats par incorporation d'unites stilbeniques et d'acide p-acetoxybenzoique
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吳重孚. "Synthesis of Substituted Cinnamic Acid Amide Analogs." Thesis, 1995. http://ndltd.ncl.edu.tw/handle/02394926598808616432.

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碩士<br>台北醫學大學<br>藥學研究所<br>83<br>A series of the cinnamic acid esters analogs had been reported in our lab. and the most potent compound was found to be 1,3-dicaffeoylpropandiol 11. The result obtained from previous investigation illustrated that the hydroxy group remained in the structure will be more efficient in platelet aggregation inhibitory activity. Since esters were considered to be relatively unstable compounds, synthesis of amide analogs were attempted. The substituted cinnamic acid derivatives including pcoumaric acid, ferulic acid, caffeic acid and p-methoxycinnamic acid, we
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Lee, Chia-hsiu, and 李嘉修. "Enzymatic synthesis of Cinnamic Acid Derivatives." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/24397101373491962989.

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碩士<br>國立臺灣科技大學<br>化學工程系<br>93<br>Ferulic acid (4-hydroxy 3-methoxy cinnamic acid), which occurred naturally in many plants, has been shown to possess photoprotective, antioxidant, antitumor and hypertensive activities. Octyl methoxycinnamate (OMC) is the most widely used non-allergic sunscreen agent in the market. Most literatures reported low conversion and long reaction time in the syntheses of ethyl ferulate and OMC. In his study, Novozym 435 was selected as the catalyst for the syntheses of ethyl ferulate from ferulic acid and ethanol, and OMC from 4-methoxycinnamic acid and 2-ethyl hex
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Chou, Shan-Yi, and 周珊沂. "Antifungal Activity of Cinnamic Acid Derivatives." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/83506275868488364942.

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碩士<br>國立臺灣大學<br>森林環境暨資源學研究所<br>103<br>Cinnamon contains many aromatic compounds, among these compounds, trans-cinnamaldehyde has been proven to possess many bioactivities, and which belongs to trans-cinnamic acid derivatives in the biosynthesis pathway. The objective of this research is to find more cinnamic acid dervitaves to against plant pathogenic fungi, wood rotting fungi and mildew, expecting to reduce the damage from fungi diseases. In order to evaluate antifungal activities of cinnamaldehyde congeners, we classified them into three groups, cinnamic acid congeners, cinnamaldehyde congen
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Books on the topic "Amide cinnamic acid derivatives"

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Buchner, Magnus R. Eta^2 Complexes of group 10 with cinnamic acid derivatives; spectroscopic properties, stability, reactivity and application potential as photo-switchable Catalysts. Logos Verlag Berlin, 2011.

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Book chapters on the topic "Amide cinnamic acid derivatives"

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Gera, Lajos, Daniel C. Chan, Vitalija Simkeviciene, Paul A. Jr Bunn, and John M. Stewart. "N-(Fluorenyl-9-methoxycarbonyl)amino Acid Amide Derivatives as a New Class of Anti-cancer Agents." In Advances in Experimental Medicine and Biology. Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-73657-0_200.

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Bassani, Dario. "The Dimerization of Cinnamic Acid Derivatives." In CRC Handbookof Organic Photochemistry and Photobiology, Volumes 1 & 2, Second Edition. CRC Press, 2003. http://dx.doi.org/10.1201/9780203495902.ch20.

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"The Dimerization of Cinnamic Acid Derivatives." In CRC Handbook of Organic Photochemistry and Photobiology, Volumes 1 & 2. CRC Press, 2003. http://dx.doi.org/10.1201/9780203495902-26.

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Barrett, Graham c. "Reductive modifications of the carboxy group." In Amino Acid Derivatives. Oxford University PressOxford, 1999. http://dx.doi.org/10.1093/oso/9780198558538.003.0014.

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Abstract The formation of aldehyde and hydroxymethyl groups is the standard out come when reductive modifications of amide, ester and carboxy groups are performed. The aldehydes have become important in the context of the synthesis of peptide mimetics, being particularly effective as progenitors of products with extended carbon chains.
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Biswas, Pronit, Rajesh Singh Yadav, and Juli Jain. "Neuroprotective Activities of Cinnamic Acids and their Derivatives." In Frontiers in Clinical Drug Research - CNS and Neurological Disorders. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815123319123110005.

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Neurodegenerative disorders are considered major global health problems associated with nervous system dysfunction, progressive neuronal cell loss with aging, and several pathological and sporadic factors. Parkinson’s disease, Alzheimer’s disease, Prion disease, Huntington’s disease, and multiple sclerosis are the main neurodegenerative diseases that raise significant concern among health scientists. The etiology of different neurodegenerative diseases is different, and they majorly affect the nervous system, including the brain, spinal cord, and peripheral nervous system. Neurodegenerative di
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Rita Estevam, Maria, Estela Mesquita, and Magali Monteiro. "Phenolic Compounds Profile of Brazilian Commercial Orange Juice." In High Performance Liquid Chromatography - Recent Advances and Applications [Working Title]. IntechOpen, 2023. http://dx.doi.org/10.5772/intechopen.109785.

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Orange juice is largely produced, exported and consumed in Brazil. It is an important source of bioactive compounds, such as flavonoids and phenolic acids, which are beneficial to the health of consumers. The aim of this work was to evaluate the phenolic compounds profile of commercial orange juice from Brazil using HPLC-DAD and UPLC-ESI-MS, and multivariate analysis. Forty-five phenolic compounds and one precursor were identified: cinnamic acid, 19 cinnamic acid derivatives, 8 flavanones and 18 flavones. Rutin, eriocitrin, narirutin, naringin, hesperidin, naringenin, nobiletin and tangeritin
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Christie, William W. "Mass spectrometry of fatty acid derivatives." In Applications of Modern Mass Spectrometry in Plant Science Research. Oxford University PressOxford, 1996. http://dx.doi.org/10.1093/oso/9780198549659.003.0013.

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Abstract The potential of mass spectrometry (MS) for the identification of fatty acids of natural origin has been evident for many years. However, until relatively recently there were few reports of structural analyses on real samples containing unsaturated fatty acids as opposed to model compounds. The topic has been the subject of several reviews (Minnikin 1978; Schmitz and Klein 1986; Jensen and Gross 1987; Murphy 1993). The main problem has been the location of double bonds, although there have also been difficulties with ring structures or branch-points. There are three general approaches
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Kantlehner, W. "From Carboxylic Acid Ortho Amide Derivatives and α,β-Unsaturated Carbonyl Compounds." In Three Carbon-Heteroatom Bonds: Ketenes and Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00457.

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Aggarwal, P., and M. W. P. Bebbington. "Reaction of Zinc(II) Bis[bis(methoxyimido)amide] with Carboxylic Acid Derivatives." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-117-00315.

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"R- AND S-DIHYDROLIPOIC ACID DERIVATIVES AS SUBSTRATES OF LIPO AMIDE DEHYDROGENASE." In Flavins and Flavoproteins 1993. De Gruyter, 1994. http://dx.doi.org/10.1515/9783110885774-093.

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Conference papers on the topic "Amide cinnamic acid derivatives"

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Quraishi, M. A. "Lauric Hydrazide Derivatives: New Class of Volatile Corrosion Inhibitors." In CORROSION 2002. NACE International, 2002. https://doi.org/10.5006/c2002-02319.

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Abstract The protection of metals against corrosion by means of volatile compounds is the most progressive method of fighting metallic corrosion. These inhibitors are used to protect metallic articles and equipment during storage and transportation. In view of this we have synthesized six organic volatile corrosion inhibitors (VCIs) using Lauric hydrazide with various acids such as cinnamic acid, succinic acid, nitrobenzoic acid, phthalic acid and maleic acid and evaluated their inhibiting action on corrosion of mild steel, copper, brass, zinc and aluminium by weight loss and potentiodynamic p
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Barmatov, Evgeny, Trevor Hughes, and Michaela Nagl. "Performance of Organic Corrosion Inhibitors on Carbon Steels and High Alloys in 4M Hydrochloric Acid." In CORROSION 2015. NACE International, 2015. https://doi.org/10.5006/c2015-05893.

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Abstract Matrix acidizing of oil and gas reservoirs is a widely established technique to increase hydrocarbon production. Strong mineral acids such as HCl or HCl/HF mixtures are injected into the well at high concentrations. For this application, corrosion inhibitors are enabling because uninhibited matrix acidizing treatment fluids would induce severe corrosion of downhole equipment. A broad range of organic film-forming corrosion inhibitors have been developed to retard the acid corrosion of coiled tubing and casing through which the acidizing fluids are injected. In this paper, the corrosio
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Zhao, Lei, Yuanbiao Tu, and Yuping Guo. "Synthesis of Cinnamic Acid Derivatives." In 2016 7th International Conference on Education, Management, Computer and Medicine (EMCM 2016). Atlantis Press, 2017. http://dx.doi.org/10.2991/emcm-16.2017.85.

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Meilawati, Lia, Endang Saepudin, and Teni Ernawati. "Antimicrobial activities of natural cinnamic acid and synthetic derivatives: Review." In XVII MEXICAN SYMPOSIUM ON MEDICAL PHYSICS. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0173189.

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VIANA, Thiago Silva, Pedro Henrique Fonseca DUQUE, Camila Prestes PINTO, et al. "SINTHESYS OF CINNAMIC ACID DERIVATIVES WITH CORROSION INHIBITION ACTIVITY FOR CARBON STEEL ALLOY." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013108103349.

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Ernawati, Teni. "Bioactivity of cinnamic acid derivatives as potential antibacterial agents based on in silico studies approach." In XVII MEXICAN SYMPOSIUM ON MEDICAL PHYSICS. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0172772.

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Ladyka, A. A., A. V. Sosnovskaya, M. V. Chernikov, and D. I. Pozdnyakov. "ANTIAPOPTOTIC EFFECT OF PHENYLACETIC ACID AMIDE DERIVATIVES. EVALUATION OF THE STRUCTURE-ACTIVITY RELATIONSHIP." In MedChem-Russia 2021. 5-я Российская конференция по медицинской химии с международным участием «МедХим-Россия 2021». Издательство Волгоградского государственного медицинского университета, 2021. http://dx.doi.org/10.19163/medchemrussia2021-2021-363.

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Mohammed, Jalal Hassan, and Saadon Abdulla Aowda. "The synthesis and biological evaluation of prodrug amide derivatives based on phenylene dioxy di acetic acid." In 2ND INTERNATIONAL CONFERENCE ON MATERIALS ENGINEERING & SCIENCE (IConMEAS 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0000138.

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Hettiger, Theresa, Arup Sarkar, Jonas Hiller, et al. "Ligand-Driven Shifts in the Electronic Properties of CsPbBr₃ Nanocrystals: Role of Cinnamic Acid Derivatives in Oxidation and Charge Injection." In MATSUS Spring 2025 Conference. FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2024. https://doi.org/10.29363/nanoge.matsusspring.2025.241.

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Reports on the topic "Amide cinnamic acid derivatives"

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Yibchok-anun, Sirintorn, and Nattaya Ngamrojanavanich. Structure-activity relationships of trans-cinnamic acid derivatives on inhibitions of alpha-glucosidase. Chulalongkorn University, 2004. https://doi.org/10.58837/chula.res.2004.86.

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Trans-Cinnamic acid and its derivatives were investigated for the a-glucosidase inhibitiory activity. 4-methoxy-trans-cinnamic acid and 4-methoxy-trans-cinnamic acid ethyl ester showed the highest potent inhibitory activity among those of trans-cinnamic acid derivatives. The presence of substituents at 4-position in trans-cinnamic acid derivatives. The presence of substituents at 4-position in trans-cinnamic acid altered the a-glucosidase inhibitory activity. Increasing of bulkiness and the chain length of 4-alkoxy substituents as well as the increasing of the electron withdrawing group have b
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