Relevant bibliographies by topics / Cinnamates

Contents

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

Academic literature on the topic 'Cinnamates'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Cinnamates"

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Sengupta, Sumana, та Avijit Banerji. "[3+2] Cycloadditions: Part XXXIV: Further Investigations of Cycloadditions of C,N-Diaryl- and C-Aryl-N-methyl Nitrones to α,β-Unsaturated Esters". Asian Journal of Chemistry 31, № 12 (2019): 2777–84. http://dx.doi.org/10.14233/ajchem.2019.22232.

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Investigations of [3+2] cycloadditions of C,N-diaryl and C-aryl-N-methyl nitrones as three atom components (TAC) to substituted methyl E-cinnamates and diethyl arylidene malonates have been further investigated. [3+2] Cycloadditions of cinnamates yielded mixtures of cycloadducts, the major products being the 3,4-trans-4,5-trans-2,3,5-triaryl-4-carbomethoxy products originating from the endo-carbonyl-exo-aryl meta channel approach of the cinnamate component. [3+2] Cycloadditions to diethyl arylidene malonates furnished single cycloadducts-3,5-trans-2-methyl-3,5-diaryl-4,4- dicarbethoxy isoxazol
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Choi, In-Ho, Ju-Yong Park, Sang-Chul Shin, and Il-Kwon Park. "Nematicidal activity of medicinal plant extracts and two cinnamates isolated from Kaempferia galanga L. (Proh Hom) against the pine wood nematode, Bursaphelenchus xylophilus." Nematology 8, no. 3 (2006): 359–65. http://dx.doi.org/10.1163/156854106778493402.

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Abstract Extracts from 40 medicinal plant species in 27 families were tested for their nematicidal activity against the pine wood nematode, Bursaphelenchus xylophilus, in 96-well plate bioassays. Responses varied with plant material and concentration. Extracts of Acorus gramineus (Araceae), Asiasarum sieboldi (Aristolochiaceae), Illicium verum (Illicaiceae) and Kaempferia galanga (Zingiberaceae) showed nematicidal activity against male, female and juvenile nematodes of B. xylophilus at 2000 μg ml−1. Among test plant species, Kaempferia galanga showed the most potent nematicidal activity. As K.
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Karpkird, Thitinun Monhaphol, Supason Wanichweacharungruang, and Bo Albinsson. "Photophysical characterization of cinnamates." Photochemical & Photobiological Sciences 8, no. 10 (2009): 1455. http://dx.doi.org/10.1039/b909695g.

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Stefanovic, Olgica, Ivana Radojevic, and Ljiljana Comic. "Synthetic cinnamates as potential antimicrobial agents." Chemical Industry 69, no. 1 (2015): 37–42. http://dx.doi.org/10.2298/hemind130928014s.

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This study deals with synthesis of methyl cinnamate, butyl cinnamate, and p-methoxy methyl cinnamate and testing of their in vitro antimicrobial activity. Antimicrobial activity was examined towards 29 microorganisms using microdilution method. It is shown that antimicrobial activity of methyl cinnamate and p-methoxy methyl cinnamate was better than that of butyl cinnamate. Sarcina lutea, Bacillus subtilis ATCC 6633, B. subtilis and B. subtilis IP 5832 (probiotic) were the most sensitive bacteria. It is established that p-methoxy methyl cinnamate can be a new, potential anti-Staphylococcus aur
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P??czkowski, Jerzy, Maria Toczek, Franciszek ??cigalski, Danuta Ćwiklińska, and Michalina Sierocka. "Cinnamates. III. The light sensitive polymers: Cinnamates with internal charge-transfer spectroscopic properties." Journal of Polymer Science Part A: Polymer Chemistry 27, no. 8 (1989): 2647–56. http://dx.doi.org/10.1002/pola.1989.080270813.

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Kunihisa, Kazuko S., and Yoshihiro Satom. "Phase transitions of cholesteryl cinnamates." Thermochimica Acta 148 (August 1989): 335–40. http://dx.doi.org/10.1016/0040-6031(89)85232-3.

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Bertsova, Y. V., M. V. Serebryakova, V. A. Anashkin, A. A. Baykov, and A. V. Bogachev. "A REDOX-REGULATED, HETERODIMERIC NADH:CINNAMATE REDUCTASE IN Vibrio ruber." Биохимия 89, no. 2 (2024): 261–78. http://dx.doi.org/10.31857/s0320972524020053ncwtx.

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Genes of putative reductases of α,β-unsaturated carboxylic acids are abundant among anaerobic and facultatively anaerobic microorganisms, yet substrate specificity has been experimentally verified for few encoded proteins. Here, we co-produced in Escherichia coli a heterodimeric protein of the facultatively anaerobic marine bacterium Vibrio ruber (GenBank SJN56019 and SJN56021; annotated as NADPH azoreductase and urocanate reductase, respectively) with Vibrio cholerae flavin transferase. The isolated protein (named Crd) consists of the sjn56021-encoded subunit CrdB (NADH:flavin, FAD binding 2,
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Pagire, Santosh K., Asik Hossain, Lukas Traub, Sabine Kerres, and Oliver Reiser. "Photosensitised regioselective [2+2]-cycloaddition of cinnamates and related alkenes." Chemical Communications 53, no. 89 (2017): 12072–75. http://dx.doi.org/10.1039/c7cc06710k.

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Mali, Raghao S., and Abhijit S. Papalkar. "Synthesis of naturally occurring cinnamyl cinnamates." Journal of Chemical Research 2001, no. 10 (2001): 433–35. http://dx.doi.org/10.3184/030823401103168370.

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Brennan, Nerida J., Lesley Larsen, Stephen D. Lorimer, et al. "Fungicidal Sesquiterpene Dialdehyde Cinnamates fromPseudowintera axillaris." Journal of Agricultural and Food Chemistry 54, no. 2 (2006): 468–73. http://dx.doi.org/10.1021/jf052585s.

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Dissertations / Theses on the topic "Cinnamates"

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Chaabouni, Slim. "Contribution à la chimie des cinnamates ortho-fonctionnalisés : Exploitation comme (1) précurseurs synthétiques d'hétérocycles, (2) antennes photoactivables de complexes d'ions lanthanides luminescents." Thesis, Toulouse 3, 2017. http://www.theses.fr/2017TOU30104/document.

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La chimie des cinnamates ortho-fonctionnalisés est particulièrement riche et variée, comme en témoigne le nombre important de méthodologies de synthèse reposant sur leur utilisation comme substrats précurseurs d'hétérocycles d'intérêt biologique. En effet, suivant la nature du groupe fonctionnel et les conditions opératoires, des substrats à base cinnamique ont déjà été exploités avec succès pour la construction d'un large panel de squelettes hétérocycliques, allant de systèmes cycliques à cinq chaînons (benzofurane, indole, ...) à des cycles à six chaînons (coumarine, quinolin(on)e, ...). Dan
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Trenor, Scott Russell. "Synthesis and Characterization of Tailored Photoactive Macromolecules." Diss., Virginia Tech, 2004. http://hdl.handle.net/10919/27314.

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Coumarin and cinnamate derivatives were positioned as either polymer chain ends or side groups to synthesize photoactive macromolecules and gain the ability to reversibly control molecular weight and crosslink density using UV light. The cinnamates and coumarins were reacted onto the polymers via multiple reaction pathways. Polymers were functionalized with coumarin or cinnamate groups via an esterification reaction between hydroxyl functionalities and an acid chloride derivatized coumarin group. In addition to the esterification reaction, cinnamates were also coupled to polymers via a ring
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Santos, Luís Rogerio Ferreira. "Reduções e oxidações eletroquímicas de cinamatos de metila ariltio e etiltio substituídos nas posições vinílicas." Universidade de São Paulo, 2008. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-10122009-092843/.

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Este trabalho apresenta o estudo do comportamento eletroquímico de cinamatos de metila sulfenilados: o 3-feniltio-3-fenil-propenoato de metila, 2-feniltio-3-fenil-propenoato de metila, 3-fenil-3-etiltio-propenoato de metila e 2-etiltio-3-fenil-proenoato de metila. Está incluído a síntese dos substratos, a voltametria e as eletrólises preparativas, abrangendo oxidações e reduções eletroquímicas. As sínteses de três dos quatro ésteres selecionados partiram de um mesmo intermediário, o 3-fenil-propinato de metila, através de reações de Michael e radicalares com etanotiol e tiofenol. O 2-etiltio-3
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Gagey, Nathalie. "Développement de nouveaux groupements protecteurs photoactivables à un et deux photons avec rapporteur fluorescent pour des applications in vivo." Paris 6, 2007. http://www.theses.fr/2007PA066206.

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Délivrer de manière contrôlée, dans l’espace et dans le temps, une quantité précise d’un substrat biologique dans un organisme est d’une importance majeure en Biologie. Couplée à l’utilisation de composés cagés, l’utilisation d’une impulsion lumineuse permet de contrôler précisément la libération du substrat dans le système. Nous avons élaboré une plate-forme de composés cagés photoactivables à un et deux-photons avec rapporteur fluorescent pour une utilisation in vivo. La synthèse de composés rationnellement conçus a été réalisée puis nous avons étudié leurs propriétés photophysiques et photo
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Le, Fur Yves. "Contribution à la connaissance aromatique des vins de Chardonnay de Bourgogne : étude des potentialités olfactives de quatre composés volatils, le cinnamate d'éthyle, le guaiacol, le cyclotène et le maltol." Dijon, 1998. http://www.theses.fr/1998DIJOS063.

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Cette étude avait pour objet de mettre en place une procédure de validation des résultats d'une analyse olfactométrique CHARM. Initialement, cette analyse a été appliquée a une population de vins de Chardonnay de Bourgogne dans le but de caractériser non seulement les zones odorantes d'intérêt dans les extraits de vins mais également les composés d'arôme qui s'y rattachaient. Sur les quinze composés identifiés et suspectés d'intervenir sur la qualité d'odeur et d'arôme des vins étudiés, la procédure de validation de ces résultats a été appliquée à quatre composés : le cinnamate d'éthyle, le gu
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Kaminishi, Tatsuya, Andreas Schedlbauer, Attilio Fabbretti, et al. "Crystallographic characterization of the ribosomal binding site and molecular mechanism of action of Hygromycin A." Oxford University Press, 2015. http://hdl.handle.net/10757/608247.

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Hygromycin A (HygA) binds to the large ribosomal subunit and inhibits its peptidyl transferase (PT) activity. The presented structural and biochemical data indicate that HygA does not interfere with the initial binding of aminoacyl-tRNA to the A site, but prevents its subsequent adjustment such that it fails to act as a substrate in the PT reaction. Structurally we demonstrate that HygA binds within the peptidyl transferase center (PTC) and induces a unique conformation. Specifically in its ribosomal binding site HygA would overlap and clash with aminoacyl-A76 ribose moiety and, therefore, its
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Chen, Jianxin. "Cinnamated PDMS Polymerization for MEMS Applications." Fogler Library, University of Maine, 2008. http://www.library.umaine.edu/theses/pdf/ChenJ2008.pdf.

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Garcia, Ricardo D\'Agostino. "Modelagem molecular (TD-DFT) aplicada à simulação de espectros UV para cinamatos com perfil de filtros solares." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/9/9138/tde-11082014-162702/.

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O câncer de pele se apresenta como um sério problema de saúde pública mundial, sendo incidente nos cinco continentes. As ações relacionadas à prevenção dessa doença envolvem, entre outras coisas, a utilização de protetores solares e a educação em saúde. Em virtude do aumento do número de indivíduos com câncer de pele a cada ano, é de grande valor estudos de entendimento e desenvolvimento de filtros solares melhores e mais seguros. Os produtos utilizados com a finalidade de proteger a pele dos raios solares ultravioletas (UV) possuem em sua composição filtros solares, que podem ter ação física,
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Sakakibara, Norikazu. "Metabolic analysis of the cinnamate/monolignol and lignan pathways." Kyoto University, 2005. http://hdl.handle.net/2433/145058.

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Kyoto University (京都大学)<br>0048<br>新制・課程博士<br>博士(農学)<br>甲第11658号<br>農博第1514号<br>新制||農||911(附属図書館)<br>学位論文||H17||N4051(農学部図書室)<br>23301<br>UT51-2005-D407<br>京都大学大学院農学研究科応用生命科学専攻<br>(主査)教授 島田 幹夫, 教授 關谷 次郎, 教授 坂田 完三<br>学位規則第4条第1項該当
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Urban, Oliver. "Experimentelle Untersuchung zur Bestimmung der Sensibilisierungspotenz ausgewählter Cinnamate und eines Kaffeates." [S.l.] : [s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=966090039.

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Books on the topic "Cinnamates"

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Tamilselvan, Kalpanadevi. Metal Hydrazine Cinnamates. Anchor Academic Publishing. ein Imprint der Diplomica Verlag GmbH, 2016.

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Mattson, Guy Charles 1927. Addition of Heterocyclic Amines to Cinnamate Esters. Creative Media Partners, LLC, 2021.

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Book chapters on the topic "Cinnamates"

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Kondo, Tetsuo, Masanori Yamamoto, Wakako Kasai, and Mitsuhiro Morita. "Synthesis and properties of regioselectively substituted cellulose cinnamates." In Polysaccharide Materials: Performance by Design. American Chemical Society, 2009. http://dx.doi.org/10.1021/bk-2009-1017.ch013.

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Bährle-Rapp, Marina. "Benzyl Cinnamate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1096.

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Bährle-Rapp, Marina. "Ethyl Cinnamate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3711.

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Siah, Lay-Foong, V. G. Kumar Das, and Seng-Neon Gan. "Copolymerisation of Substituted Tributyltin Cinnamates with Styrene. Syntheses, Reactivity Ratios, Relative Reactivities, NMR and Mössbauer Assignments and Thermal Analysis." In Main Group Elements and their Compounds. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-52478-3_25.

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Lide, David R. "Ethyl trans-cinnamate." In Handbook of Organic Solvents. CRC Press, 2024. http://dx.doi.org/10.1201/9781003575191-216.

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Bährle-Rapp, Marina. "Diisopropyl Methyl Cinnamate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3025.

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Schomburg, Dietmar, and Dörte Stephan. "trans-Cinnamate 4-monooxygenase." In Enzyme Handbook. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-57942-4_93.

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Schomburg, Dietmar, and Dörte Stephan. "trans-Cinnamate 2-monooxygenase." In Enzyme Handbook. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-57942-4_96.

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Schomburg, Dietmar, and Dörte Stephan. "Cinnamate beta-D-glucosyltransferase." In Enzyme Handbook 12. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61117-9_177.

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Masselink, Wouter, and Elly M. Tanaka. "Ethyl Cinnamate-Based Tissue Clearing Strategies." In Methods in Molecular Biology. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2659-7_7.

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Conference papers on the topic "Cinnamates"

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Quraishi, M. A., M. Natesan, and Sudheer. "Ethanolamine Salt as Vapor Corrosion Inhibitors for Mild Steel in NaCl Environment." In CORROSION 2012. NACE International, 2012. https://doi.org/10.5006/c2012-01236.

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Abstract Three new volatile corrosion inhibitors (VCIs) such as ethanolamine benzoate (EAB), ethanolamine salicylate (EAS), and ethanolamine cinnamate (EAC), were synthesised and investigated as vapor corrosion inhibitors by weight loss, potentiodynamic polarization, and electrochemical impedance methods for mild steel. The potentiodynamic polarization studies have shown that EAB, EAC are mix type inhibitor behaviour and EAS behaved predominantly as anodic corrosion inhibitor. All the investigated VCIs exhibited good inhibition efficiency (IE) for mild steel.
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Subramanian, P., David Creed, Charles E. Hoyle, and Krishnan Venkataram. "Triplet-sensitized reactions of some main chain liquid-crystalline polyaryl cinnamates." In San Diego, '91, San Diego, CA, edited by Roger A. Lessard. SPIE, 1991. http://dx.doi.org/10.1117/12.50695.

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Singh, Sangya, David Creed, and Charles E. Hoyle. "Photophysics and photochemistry of side-chain substituted liquid crystalline polyaryl cinnamates." In San Diego '92, edited by Roger A. Lessard. SPIE, 1993. http://dx.doi.org/10.1117/12.139164.

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Barancelli, Daniela Aline, Airton G. Salles Jr., Jason G. Taylor, and Carlos Roque D. Correia. "Coumarins from Free ortho-Hydroxy Cinnamates by Heck- Matsuda Arylations and their Application in the Total Synthesis of (R)-Tolterodine." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013816201342.

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Thiemann, Thies, Mariam Al Azani, and John Graham. "Preparation and Photochemistry of 3-O-Methylestra-1,3,5(10)-Triene-17beta-yl Cinnamates and 3-O-Methylestra-1,3,5(10)-Trien-17-one O-Cinnamoyl-17-Oximes." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a039.

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YANG, SHUIJIN, XIEQING YU, YONGGUANG LIANG, and JUTANG SUN. "CATALYTIC SYNTHESIS OF N-AMYL CINNAMATE WITH TiSiW12O40/TiO2." In Proceedings of the International Symposium on Solid State Chemistry in China. WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812776846_0046.

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Wojciechowski, Piotr, Lidia Okrasa, and Marcin Kozanecki. "Mesomorphism and photocuring processes of (2-hydroxypropyl) cellulose cinnamate." 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/10.1117/12.472155.

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Romanov, I., Mario Barbatti, Mariana Telles do Casal, Josene Toldo, Wybren Buma, and Y. Boeije. "HIGH-RESOLUTION LASER SPECTROSCOPIC STUDIES OF CINNAMATE-BASED MOLECULAR HEATERS." In 2022 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2022. http://dx.doi.org/10.15278/isms.2022.rh03.

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Joshi, Sonia, та Mayur Gaikwad. "Effects of Methyl Cinnamate on GMR-Aβ42 D. melanogaster Larvae". У 19th National Research Scholar s Meet 2023. Thieme Medical and Scientific Publishers Pvt. Ltd., 2024. http://dx.doi.org/10.1055/s-0044-1788219.

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Bhuvaneswari, R., B. Subash, and K. Sakthi Murugesan. "Spectral, optical and quantum chemical analysis of morpholinium cinnamate single crystal." In PROF. DINESH VARSHNEY MEMORIAL NATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF MATERIALS: NCPCM 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5098607.

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Reports on the topic "Cinnamates"

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วนิชเวชารุ่งเรือง, ศุภศร. การศึกษาความเสถียรและผลิตภัณฑ์จากการสลายตัวของสารกรองรังสียูวี Octyl Methoxycinnamate : รายงานผลการวิจัย. จุฬาลงกรณ์์มหาวิทยาลัย, 2001. https://doi.org/10.58837/chula.res.2001.86.

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การศึกษาความเสถียรของ octyl methoxycinnamate (OMC) โดยใช้ C-18 HPLC บ่งชี้ว่า OMC จะสลายตัวไปเป็นผลิตภัณฑ์ใหม่เมื่อถูกแสงแดด เมื่อเก็บ OMC ไว้ในที่มืดที่ 4, 20,32 และ 60 องศาเซลเซียส เป็นเวลา 1 เดือน ไม่พบการสลายตัวของ OMC การทำ online HPLC-APCI-MS ของ OMC และผลิตภัณฑ์ที่เกิดจากการสลายตัวให้ APCI mass spectra ที่เหมือนกัน ได้ทำการแยก photo-degradation product โดยวิธี semi-preparative HPLC นำสารที่แยกได้ไปตรวจสอบ NMR spectra ผลการทดลองบ่งชี้ว่ามีการเปลี่ยน configuration จาก octyl-p-methoxy-trans-cinnamate ไปเป็น octyl-p-methoxy-cis-cinnamate NMR spectra ของ OMC ที่ตากแดดและยังไม่ผ่านการแยก บ่งช
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Allock, Harry R., and Charles G. Cameron. The Synthesis and Characterization of Small Molecule and Photo-Cross- Linkable High Polymeric Phosphazenes Bearing Cinnamate Groups. Defense Technical Information Center, 1994. http://dx.doi.org/10.21236/ada279782.

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Aggarwal, R. L., L. W. Farrar, B. G. Saar, T. H. Jeys, and R. B. Goodman. Measurement of the Absolute Raman Cross Sections of Diethyl Phthalate, Dimethyl Phthalate, Ethyl Cinnamate, Propylene Carbonate, Tripropyl Phosphate, 1,3-Cyclohexanedione, 3'-Aminoacetophenone, 3'-Hydroxyacetophenone, Diethyl Acetamidomalonate, Isovanillin, Lactide, Meldrum's Acid, p-Tolyl Sulfoxide, and Vanillin. Defense Technical Information Center, 2013. http://dx.doi.org/10.21236/ada591110.

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