Academic literature on the topic 'Enoic Acid'

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Journal articles on the topic "Enoic Acid"

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Allan, RD, HW Dickenson, GAR Johnston, R. Kazlauskas, and HW Tran. "Synthesis of Analogues of GABA. XIV. Synthesis and Activity of Unsaturated Derivatives of 5-Aminopentanoic Acid (d-Aminovaleric Acid)." Australian Journal of Chemistry 38, no. 11 (1985): 1651. http://dx.doi.org/10.1071/ch9851651.

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The (Z) and (E) pairs of 5-aminopent-2-enoic acid and 5-aminopent-3- enoic acid, as well as the related 5-aminopent-3-ynoic acid, have been prepared for structure-activity studies on GABA receptors. Only the (Z) isomers were active as GABA agonists with (Z)-5-aminopent-2-enoic acid being two- to four-fold more active than 5-aminopentanoic acid.
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F., G. BADDAR, N. BASYOUNI M., F. EI-NEWAIRY M. та H. GHALY E. "ᵧ.ᵧ-Disubstituted Itaconic Acids. Part Vll.1 The Stobbe Condensation of Benzyl-, p-Chlorobenzyl-, and p-Methoxybenzylphenyl Ketones with Diethyl Succinate". Journal of Indian Chemical Society Vol. 51, Jul 1974 (2022): 698–704. https://doi.org/10.5281/zenodo.6417065.

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Department of <em>Chemistry, </em>Faculty of Science, A&#39; in Shams <em>University, Cairo, Egypt.</em> <em>Manuscript received 22 October 1973 ; acepted 23 May 1974.</em> <em>\(Cis \)</em>(Ph/Ar)-5-Aryl-3-ethoxycarbonyl-4-phenyl-pent-4-enoic acids were converted into ethyl <em>\(trans\)-</em>(Ph/Ar)<em><sup>-</sup> 5-aryl-3-</em>carboxy-4-phenyl-pent-4-enoute (14), (15) and (16), which have been cyclised<em> </em>to 1-acetoxy-naphthalenes (17), (18) <em>and </em>(19). <em>\(Cis\) </em>(Ph/ Ar)<em>-4, </em>5-Diphenyl- <em>and </em>cis (Ph/Ar)-4-phenyl-5-p-tolyl-pent-4-enoic acid anhydrides<em> </em>were converted with aluminium chloride<em> </em>to<em> a </em>mixture of the corresponding cyclopentenones and arylidene tetralone carboxylic acids<em>. \(Trans \)(Ph/CO<sub>2</sub></em>E<em>t)-5-Aryl-3-</em>ethoxycarbonyl-4-phenyl-pent-3-enolc acids were cyclised to ethyl 4-acetoxY-1-arylmethyl-2-naphthoates.
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Zhang, Jun, Kaida Zhou, and Jie Wu. "Generation of sulfonated isobenzofuran-1(3H)-ones under photocatalysis through the insertion of sulfur dioxide." Organic Chemistry Frontiers 5, no. 5 (2018): 813–16. http://dx.doi.org/10.1039/c7qo00987a.

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Generation of sulfonated isobenzofuran-1(3H)-ones starting from 2-vinylbenzoic acids, aryldiazonium tetrafluoroborates, and DABCO˙(SO<sub>2</sub>)<sub>2</sub> under photocatalysis in the presence of visible light is achieved. Additionally, the method can be extended to 4-phenylpent-4-enoic acid and 5-phenylhex-5-enoic acid.
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Abou-ElWafa, Ghada S. E., Mohamed Shaaban, Khaled A. Shaaban, Mohamed E. E. El-Naggar, and Hartmut Laatsch. "Three New Unsaturated Fatty Acids from the Marine Green Alga Ulva fasciata Delile." Zeitschrift für Naturforschung B 64, no. 10 (2009): 1199–207. http://dx.doi.org/10.1515/znb-2009-1014.

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From the dichloromethane extract of the marine green alga Ulva fasciata Delile, collected from the Mediterranean coast of Egypt, three new fatty acids, namely, (E)-11-oxo-octadeca-12-enoic acid (1a), (E)-11-hydroxy-octadeca-12-enoic acid (2a) and 6-hydroxy-oct-7-enoic acid (3a) together with cholesterol were isolated. Analysis of the unpolar part of the extract using GC-MS detected the existence of further ten compounds, namely, dimethylsulfoxide, dimethylsulfone, phenylacetamide, 6,10,14-trimethyl-pentadecan-2-one, 8-heptadecene, dodecane, tridecane, 4-oxo-pentanoic acid, hexadecanoic acid, and the naturally new 1,1ʹ-bicyclohexyl. Structures of the isolated compounds 1a - 3a were confirmed by spectroscopic analyses including mass spectra (EI-MS, HR/ESIMS), 1D and 2D NMR experiments, and by the synthetic conversion into their corresponding methyl esters 1b - 3b. The algal extract and its components were comparatively examined against several pathogenic microorganisms, and brine shrimps for cytotoxicity.
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Teichert, Axel, Tilo Lübken, Jürgen Schmidt, Andrea Porzel, Norbert Arnold, and Ludger Wessjohann. "Unusual Bioactive 4-Oxo-2-alkenoic Fatty Acids from Hygrophorus eburneus." Zeitschrift für Naturforschung B 60, no. 1 (2005): 25–32. http://dx.doi.org/10.1515/znb-2005-0105.

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From fruit bodies of the basidiomycete Hygrophorus eburneus (Bull.: Fr.) Fr. (Tricholomataceae) eight fatty acids (C16, C18) with γ -oxocrotonate partial structure could be isolated. Initial tests demonstrate their bactericidal and fungicidal activity. The structures of (2E,9E)-4-oxooctadeca- 2,9,17-trienoic acid (1), (2E,11Z)-4-oxooctadeca-2,11,17-trienoic acid (2), (E)-4-oxohexadeca-2,15- dienoic acid (3), (E)-4-oxooctadeca-2,17-dienoic acid (4), (2E,9E)-4-oxooctadeca-2,9-dienoic acid (5), (2E,11Z)-4-oxooctadeca-2,11-dienoic acid (6), (E)-4-oxohexadec-2-enoic acid (7), and (E)-4- oxooctadec-2-enoic acid (8) were elucidated on the basis of their spectroscopic data.
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Sonneck, Marcel, Tim Peppel, Anke Spannenberg, and Sebastian Wohlrab. "Crystal structure of (E)-dodec-2-enoic acid." Acta Crystallographica Section E Crystallographic Communications 71, no. 7 (2015): o528—o529. http://dx.doi.org/10.1107/s2056989015011937.

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The crystal structure of (E)-dodec-2-enoic acid, C12H22O2, an α,β-unsaturated carboxylic acid with a melting point (295 K) near room temperature, is characterized by carboxylic acid inversion dimers linked by pairs of O—H...O hydrogen bonds. The carboxylic acid group and the following three carbon atoms of the chain of the (E)-dodec-2-enoic acid molecule lie almost in one plane (r.m.s. deviation for the four C atoms and two O atoms = 0.012 Å), whereas the remaining carbon atoms of the hydrocarbon chain adopt a nearly fully staggered conformation [moduli of torsion angles vary from 174.01 (13) to 179.97 (13)°].
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Gauthier, Kathryn M., Christina Deeter, U. Murali Krishna, et al. "14,15-Epoxyeicosa-5( Z )-enoic Acid." Circulation Research 90, no. 9 (2002): 1028–36. http://dx.doi.org/10.1161/01.res.0000018162.87285.f8.

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Sonneck, Marcel, Tim Peppel, Anke Spannenberg, and Sebastian Wohlrab. "Synthesis and Molecular Structures of (E)-non-2-enoic Acid and (E)-dec-2-enoic Acid." Crystals 5, no. 4 (2015): 466–74. http://dx.doi.org/10.3390/cryst5040466.

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FENG, Jun, Jing SHI, Sarath R. SIRIMANNE, Corinne E. MOUNIER-LEE, and Sheldon W. MAY. "Kinetic and stereochemical studies on novel inactivators of C-terminal amidation." Biochemical Journal 350, no. 2 (2000): 521–30. http://dx.doi.org/10.1042/bj3500521.

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C-terminal amidation, a required post-translational modification for the bioactivation of many neuropeptides, entails sequential enzymic action by peptidylglycine α-mono-oxygenase (PAM, EC 1.14.17.3) and peptidylamidoglycolate lyase (PGL, EC 4.3.2.5). Here we introduce novel compounds in which an olefinic functionality is incorporated into peptide analogues as the most potent turnover-dependent inactivators of PAM. Kinetic parameters for PAM inactivation by 4-oxo-5-acetamido-6-phenyl-hex-2-enoic acid and 4-oxo-5-acetamido-6-(2-thienyl)-hex-2-enoic acid were obtained by using both the conventional dilution assay method and the more complex progress curve method. The results obtained from the progress curve method establish that these compounds exhibit the kinetic characteristics of pure competitive inactivators (i.e. no ESI complex forms during inactivation). On the basis of kinact/Ki values, 4-oxo-5-acetamido-6-(2-thienyl)-hex-2-enoic acid is almost two orders of magnitude more potent than benzoylacrylate, a chemically analogous olefinic inactivator that lacks the peptide moiety. Stereochemical studies established that PAM inactivation by 4-oxo-5-acetamido-6-(2-thienyl)-hex-2-enoic acid is stereospecific with respect to the moiety at the P2 position, which is consistent with previous results with substrates and reversible inhibitors. In contrast, 2,4-dioxo-5-acetamido-6-phenylhexanoic acid, which is a competitive inhibitor with respect to ascorbate, exhibits a low degree of stereospecificity in binding to the ascorbate sites of both PAM and dopamine-β-hydroxylase.
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Vijender, Singh, Ali Mohammed, Malik Archana, and Sultana Shahnaz. "New aliphatic constituents from the aerial parts of Artemisia annua L." Algerian Journal of Natural Products 5, no. 2 (2017): 515–23. https://doi.org/10.5281/zenodo.1117151.

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<em>Artemisia annua</em> L. (Asteraceae) is an aromatic annual herb, up to 2 m in height, found in temperate Asia, especially China and naturalized in many countries of the world.&nbsp; The plant is prescribed against fever, malaria, skin diseases, jaundice, malignant ulcers and haemorrhoids. Phytochemical investigation of the aerial parts of <em>A. annua</em> led to the isolation of alkyl alcohols, fatty acid esters, alkyl glucoside and fatty acids characterized as <em>n-</em>nonadecan-2&beta;-ol (isononadecanol, <strong>1</strong>), <em>n-</em>docosan-9&beta;-ol (isodocosanol, <strong>&nbsp;2</strong>), 1<em>-</em>octacosanol (<em>n-</em>octacosanyl alcohol,<strong> 3</strong>), <em>n</em>-heptadecanyl <em>n</em>-octadec-9,12-dienoate (<em>n</em>-heptadecanyl linoleate, <strong>&nbsp;4</strong>), <em>n</em>-octadecanyl <em>n-</em>octadec-9,12,-dienoate (<em>n</em>-octadecanyl linoleate, <strong>5</strong>), <em>n</em>-nonacosanyl <em>n</em>-octadec-9, 12-dienoate (<em>n</em>-nonacosanyl linoleate,<strong> 6</strong>), <em>n</em>-cos-(Z)-10-enoic acid (<em>cis</em>-cos-10-enoic acid, <strong>7</strong>), <em>n</em>-cos-(Z)-9-enoic acid (<em>cis-c</em>os-9-enoic acid<strong>, 8</strong>) and <em>n-</em>heptadecanyl-&szlig;-D-glucopyronoside (<em>n</em>-heptadecanyl glucoside,<strong> 9</strong>). The structures of all phytoconstituents, isolated for the first time from <em>A. annua</em> have been elucidated on the basis of spectral data analysis and chemical reactions
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Dissertations / Theses on the topic "Enoic Acid"

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Wang, Hua. "PART I: FORMATION, PROTEIN MODIFICATION, AND CELLULAR METABOLISM OF 4-HYDROXY-7-OXOHEPT-5-ENOIC ACID LACTONE (HOHA-LACTONE)PART II: DETECTION AND BIOLOGICAL ACTIVITIES OF CARBOXYETHYLPYRROLE (CEP)-PHOSPHATIDYL-ETHANOLAMINE AND METABOLISM OF CEP-LYSINE." Case Western Reserve University School of Graduate Studies / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=case1386252158.

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Tomko, Nicholas Daniel. "Docosahexaenoate Oxidation in the Progression of Glioblastoma: Mechanistic Studies and Evaluation of a Therapeutic Antibody." Case Western Reserve University School of Graduate Studies / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1544194949142565.

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Books on the topic "Enoic Acid"

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Wardell, Ian. Heterodiene cycloadditions of enoic acid derivatives: Synthetic scope and limitations. University of Salford, 1989.

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Book chapters on the topic "Enoic Acid"

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Wohlfarth, Ch. "Viscosity of cis-octadec-9-enoic acid." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_396.

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Wohlfarth, Christian. "Viscosity of cis-octadec-9-enoic acid." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_397.

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Wohlfarth, Ch. "Surface tension of cis-octadec-9-enoic acid." In Supplement to IV/16. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75508-1_185.

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Winkelmann, Jochen. "Self-diffusion coefficient of cis-octadec-11-enoic acid." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_257.

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Winkelmann, Jochen. "Self-diffusion coefficient of cis-octadec-9-enoic acid." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_258.

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Winkelmann, Jochen. "Self-diffusion coefficient of cis-octadec-6-enoic acid." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_259.

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Winkelmann, Jochen. "Self-diffusion coefficient of trans-octadec-9-enoic acid." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_260.

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Wohlfarth, Ch. "Viscosity of the mixture (1) hexadecanoic acid; (2) cis-octadec-9-enoic acid." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_1869.

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Wohlfarth, Ch. "Viscosity of the mixture (1) cis-octadec-9-enoic acid; (2) octadecanoic acid." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_1872.

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Winkelmann, Jochen. "Diffusion coefficient of cis-octadec-9-enoic acid in methanol." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_1108.

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Conference papers on the topic "Enoic Acid"

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Shanmugam, Kotteswaran, Senthil Pandian M., and Ramasamy P. "Synthesis and characterization of organic 2-(cyano 3-(4-diphenylamino) phenyl) prop 2-enoic acid dye for electrochemical cell applications." In DAE SOLID STATE PHYSICS SYMPOSIUM 2018. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5113403.

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Shipilovskikh, Sergei A., R. R. Makhmudov, S. Yu Balandina, and Aleksandr E. Rubtsov. "Search of antimicrobial activity in a series of substituted 4-aryl-4-oxo-2-tienilaminobut-2-enoic acids." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0018494.

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Promponas, Vasilis J. "A simple clustering approach for pathogenic strain identification based on local and global amino acid compositional signatures from enomic sequences: the Escherichia genus case." In 2009 9th International Conference on Information Technology and Applications in Biomedicine (ITAB 2009). IEEE, 2009. http://dx.doi.org/10.1109/itab.2009.5394396.

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