Relevant bibliographies by topics / Ether(alkyl allyl)

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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 'Ether(alkyl allyl)'

Author: Grafiati
Published: 4 June 2021
Last updated: 14 February 2022

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Journal articles on the topic "Ether(alkyl allyl)"

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Ollevier, Thierry, and Topwe M. Mwene-Mbeja. "Diastereoselective bismuth triflate catalyzed Claisen rearrangement of 2-alkoxycarbonyl-substituted allyl vinyl ethers." Canadian Journal of Chemistry 86, no. 3 (March 1, 2008): 209–12. http://dx.doi.org/10.1139/v07-149.

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In the presence of a catalytic amount of bismuth triflate, 2-alkoxycarbonyl-substituted allyl vinyl ethers as a mixture of enol ether double bond isomers were smoothly converted into the β,γ-alkyl-substituted α-keto esters. The isomerization reaction proceeded rapidly to afford smoothly the α-keto esters in good to excellent yields using catalytic amounts of Bi(OTf)3·4H2O (1 mol%). (Z,Z)-2-iso-Propyloxycarbonyl-substituted allyl vinyl ethers 3Z,Z afforded the corresponding β,γ-alkyl-substituted α-keto esters 4 with very good syn diastereoselectivity.Key words: bismuth; bismuth(III) triflate; Claisen rearrangement; allyl vinyl ethers.
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Liu, Michael T. H., Yuri N. Romashin, and T. K. Venkatachalam. "Photolysis of 3-chloro-3-aryldiazirines in the presence of amines and allyl alcohol." Canadian Journal of Chemistry 72, no. 9 (September 1, 1994): 1961–65. http://dx.doi.org/10.1139/v94-250.

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When photolysis of arylchlorodiazirines is performed in the presence of either alkyl- or allyl-substituted amines, either N-alkyl- or N-allyl-substituted amines result as the sole high-yield (64-93%) products. Photolysis in the presence of phenylallylamine produces a rearranged product in poor yield (11–15%) whereas the reaction of allyl alcohol with arylchlorocarbene gives exclusively diallyl acetals in high yield (70%). The rate constants for these reactions were obtained by laser flash photolysis. Allyl phenyl ether forms a cyclopropanated product when treated with arylchlorocarbene. The different behaviour of these compounds may be attributed to the nucleophilicity at the nitrogen and oxygen centres of these compounds, when the latter are subjected to the substitutions described above. The formation of a cyclopropanated product when allyl phenyl ether is used differs from the reaction of bis (methoxycarbonyl) carbene with allyl ethers, as reported in the literature. The formation of this cyclopropanated product demonstrates the absence of an oxonium ylide intermediate during the reaction.
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Tian, Juan, Dayong Sang, Xiaodong Tu, Zhoujun He, and Ming Yao. "Cleavage of Catechol Monoalkyl Ethers by Aluminum Triiodide–Dimethyl Sulfoxide." Synthesis 51, no. 03 (September 26, 2018): 704–12. http://dx.doi.org/10.1055/s-0037-1610996.

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Using eugenol and vanillin as model substrates, a practical method is developed for the cleavage o-hydroxyphenyl alkyl ethers. Aluminum oxide iodide (O=AlI), generated in situ from aluminum triiodide and dimethyl sulfoxide, is the reactive ether cleaving species. The method is applicable to catechol monoalkyl ethers as well as normal phenyl alkyl ethers for the removal of methyl, ethyl, isopropyl, and benzyl groups. A variety of functional groups such as alkenyl, allyl, amide, cyano, formyl, keto, nitro, and halogen are well tolerated under the optimum conditions. Partial hydrodebromination was observed during the demethylation of 4-bromoguaiacol, and was resolved using excess DMSO as an acid scavenger. This convenient and efficient procedure would be a practical tool for the preparation of catechols.
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Hanessian, Stephen, Hubli Prabhanjan, Dongxu Qiu, and Sudhir Nambiar. "Synthesis of chemically and functionally diverse scaffolds from pentaerythritol." Canadian Journal of Chemistry 74, no. 9 (September 1, 1996): 1731–37. http://dx.doi.org/10.1139/v96-191.

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Pentaerythritol (2,2-bis-hydroxymethyl-propane-1,3-diol) was converted into a series of mono-, di-, and trisubstituted derivatives, comprising allyl ethers and amino-alkyl ethers, by systematic chemical manipulation of the hydroxy groups. The remaining hydroxymethyl group in the case of the trisubstituted analog was functionalized with ether groups bearing terminal ω-carboxyl or ω-alkene groups. These derivatives are versatile templates and scaffolds for single, double, or triple substitution with appropriate ligands forming amides and esters, and allowing the attachment of the ω-alkene or ω-carboxyl group to solid support for combinatorial chemistry. Key words: molecular diversity, scaffolds, templates and tris(2-aminoethyl)-pentaerythritol.
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Maeda, Satoshi, Tomoyo Mohri, Tsubasa Inoue, Yoshio Asano, Yurika Otoki, Masaru Enomoto, Kiyotaka Nakagawa, Shigefumi Kuwahara, and Yusuke Ogura. "Synthesis of a plasmenylethanolamine." Bioscience, Biotechnology, and Biochemistry 85, no. 6 (March 11, 2021): 1383–89. http://dx.doi.org/10.1093/bbb/zbab037.

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ABSTRACT A concise synthesis of a plasmenylethanolamine (PlsEtn-[16:0/18:1 n-9]), known as antioxidative phospholipids commonly found in cell membranes, has been achieved from an optically active known diol through 8 steps. The key transformations for the synthesis of PlsEtn-[16:0/18:1 n-9] are (1) regio- and Z-selective vinyl ether formation via the alkylation of a lithioalkoxy allyl intermediate with an alkyl iodide, and (2) a one-pot phosphite esterification–oxidation sequence to construct the ethanolamine phosphonate moiety in the presence of the vinyl ether functionality. The piperidine salt of synthetic PlsEtn-[16:0/18:1 n-9] was desalinated through reversed-phase high-performance liquid chromatography purification.
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Zaragoza-Galicia, Ivann, Zaira A. Santos-Sánchez, Yazmín I. Hidalgo-Mercado, Horacio F. Olivo, and Moisés Romero-Ortega. "Synthesis of 5-Substituted 2-Pyrrolidinones by Coupling of Organozinc Reagents with Cyclic N-Acyliminium Ions." Synthesis 51, no. 24 (October 8, 2019): 4650–56. http://dx.doi.org/10.1055/s-0037-1610733.

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A coupling reaction between cyclic N-acyliminium ions with organozinc reagents is described. The cyclic N-acyliminium ions, generated in situ from N-substituted-5-hydroxy-2-pyrrolidinones by treatment with boron trifluoride–diethyl ether complex or titanium tetrachloride, are trapped by the organozinc reagent, which is formed from an alkyl bromide in the presence of zinc in the same reaction medium. The N-substituted-5-allyl-2-pyrrolidinones generated using this method serve as versatile intermediates for the synthesis of azabicyclic systems with indolizidine and pyrroloazepinolizidine cores.
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Witzke, N. M., and R. Bittman. "Convenient synthesis of racemic mixed-chain ether glycerophosphocholines from fatty alkyl allyl ethers: useful analogs for biophysical studies." Journal of Lipid Research 27, no. 3 (January 1987): 344–51. http://dx.doi.org/10.1016/s0022-2275(20)38840-4.

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Pincock, A. L., and J. A. Pincock. "The structure, photochemical reactivity, and photophysical properties of adamantyl X-substituted aryl ethers and a comparison with the alkyl groups, methyl, tert-butyl, and allyl." Canadian Journal of Chemistry 83, no. 9 (September 1, 2005): 1237–52. http://dx.doi.org/10.1139/v05-117.

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The structure, photophysical properties, and photochemistry of the adamantyl aryl ethers 1 in both methanol and cyclohexane have been examined. UV absorption spectra, 13C NMR chemical shifts, X-ray structures, and Gaussian calculations (B3LYP/6-31G(d)) indicate that these ethers adopt a 90° conformer in the ground state. In contrast, fluorescence spectra, excited singlet state lifetimes, and calculations (TDDFT) indicated a 0° conformer is preferred in the first excited singlet state S1. Irradiation in either solvent results in the formation of adamantane and the corresponding phenol as the major products, both derived from radical intermediates generated by homolytic cleavage of the ether bond. The 4-cyano substituted ether 1j was the only one to form the ion-derived product, 1-methoxyadamantane (16% yield), on irradiation in methanol. Rate constants of bond cleavage for these ethers from S1 were estimated by two different methods by comparison with the unreactive anisoles 2, but the effect of substituents was too small to determine structure–reactivity correlations. The temperature dependence of the quantum yields of the fluorescence of the unsub stituted, 4-methoxy and 4-cyano derivatives of 1 and 2 were also determined. These results indicated that the activated process for 1 was mainly bond cleavage for the 4-cyano substrate whereas for 2, it was internal conversion and intersystem crossing. Key words: aryl ether photochemistry, fluorescence, excited-state rate constants, excited-state temperature effects.
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Nasser, Boubker, Claude Morpain, Bernard Laude, and Norbert Latruffe. "Synthesis and characterization of chemical intermediates of acyl or alkyl phospholipids." Canadian Journal of Chemistry 70, no. 8 (August 1, 1992): 2319–24. http://dx.doi.org/10.1139/v92-293.

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Precursors of phospholipids or ether lipids were synthesized from D-mannitol, i.e., 1-O-myristoyl-2-O-benzyl-sn-glycerol 11 and 1-O-hexadecyl-2-O-benzyl-sn-glycerol 13. The chemical pathways involved sequential protection reactions using allyl, triphenylmethyl, or benzyl groups via 3-O-allyl-sn-glycerol. Eleven intermediates were isolated and for the first time characterized with their spectrometric (especially 1H nmr) and physical parameters and yield. This work allowed preparation of chemically defined membrane phospholipids from compound 11 as well as ether lipids from compound 13 with cell mediator activities bearing different probes such as photoactivatable, fluorescent, or radioactive groups.
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He, Min, and Qiuyu Zhang. "Application of Ammonium α-Allyl Alkyl Phenol Polyoxyethylene Ether Sulfonate in Acrylic Emulsion Pressure-Sensitive Adhesive." Polymer-Plastics Technology and Engineering 50, no. 15 (November 2011): 1570–75. http://dx.doi.org/10.1080/03602559.2011.603788.

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Dissertations / Theses on the topic "Ether(alkyl allyl)"

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Pollex, Annett. "Viridiofungins and xeniolide F: target oriented synthesis using different rearrangement reactions of a common substrate class." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2006. http://nbn-resolving.de/urn:nbn:de:swb:14-1160474365794-44380.

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The present dissertation covers the total synthesis of viridiofungin triesters and studies toward the total synthesis of xeniolide F. In both cases, sigmatropic rearrangements of α-allyloxy substituted α,β-unsaturated esters are employed: for the viridiofungin ester synthesis a [2,3]-Wittig rearrangement and for the xeniolide F synthesis a catalytic asymmetric Claisen rearrangement CAC. For both rearrangement reactions the historical development, main characteristic and important variations are discussed. The viridiofungin triester synthesis represents a convergent and highly flexible route toward these natural products. The [2,3]-Wittig rearrangement allowed the diastereoselective synthesis of the polar head group with two adjacent stereogenic centers. The E-configured double bond was formed by a Julia-Kocienski olefination. During the studies toward the total synthesis of xeniolide F a new, diastereoselective strategy for the generation of allyl vinyl ethers with E-configured vinyl ether double bond was established employing rhodium catalyzed OH-insertion and an E-selective Horner-Wadsworth-Emmons olefination. Under the conditions of the catalytic asymmetric Claisen rearrangement (CAC) this highly substituted allyl vinyl ether rearranged diastero- and enantioselectively to the corresponding a-keto ester. This example clearly illustrates the high potential of the CAC as synthetic tool for natural product synthesis
In der vorliegenden Arbeit wird die Totalsynthese von Tirestern der Viridiofungine A, A2 und A4 sowie die Synthese eines Schlüsselintermediates für die Totalsynthese von Xeniolid F dargestellt. In beiden Fällen wird ausgehend von einem α-allyloxysubstituierten α,β-ungesättigten Ester eine Umlagerungsreaktion als Schlüsselschritt eingesetzt: im Falle der Viridiofunginester eine diastereoselektive [2,3]-Wittig-Umlagerung, bei den Arbeiten zur Totalsynthese von Xeniolid F eine diastero- und enantioselektive, katalytische Claisenumlagerung. Für beide Umlagerungsreaktionen werden ausführlich die theoretischen Hintergründe sowie die historische Entwicklung und wichtige Varianten besprochen. Mit der Viridiofungintriestersynthese wird eine konvergente und bezüglich der lipophilen Seitenkette sehr flexible Syntheseroute vorgestellt. Die [2,3]-Wittig-Umlagerung konnte dabei erfolgreich für die diastereoselektive Synthese der hochsubstituierten, polaren Kopfgruppe der Viridiofunginester mit zwei benachbarten stereogenen Zentren (davon eines quartär) eingesetzt werden. Zur Bildung der E-konfigurierten Doppelbindung wurde die Julia-Kocienskie-Olefinierung ausgenutzt. Bei den Arbeiten zur Totalsynthese von Xeniolid F wurde eine neuartige Strategie zur diastereoselektiven Synthese eines Allylvinylethers mit E-konfigurierter Vinyletherdoppelbindung eingesetzt. Die Horner-Wadsworth-Emmons-Olefinierung (HWE-Olefinierung) generierte dabei E-selektiv die Vinyletherdoppelbindung. Das für die HWE-Olefinierung benötigte Phosphonat wurde durch rhodiumkatalysierte OH-Insertion aus einem Allylalkohol und einem Diazaphosphonoacetat hergestellt. Der hochsubstituierte Allylvinylether wurde unter den Bedingungen der katalytisch asymmetrischen Claisenumlagerung umgesetzt und führte mit exzellenter Diastereo- und Enantioselektivität zum entsprechenden α-Ketoester. Anhand dieses Beispiels konnte das Potential der katalytisch asymmetrischen Claisenumlagerung zum Aufbau von hochfunktionalisierten Bausteinen für die Naturstoffsynthese verdeutlicht werden
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Wan, Jung Wing. "Novel ether lipids as antineoplastic agents." Thesis, University of Southampton, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242627.

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Cerone, Matthew. "Synthesis of Alkyl Substituted Phenylated Poly(Ether Ether Ketone Ketone)s." Wright State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=wright1496856789109456.

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Greenhalgh, Richard P. "Diasteroselective Wittig rearrangements." Thesis, University of Kent, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.359407.

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Cho, Chang Gi. "Controlled polymerization of alkyl vinyl ethers via 'covalent' propagating species." Diss., Virginia Polytechnic Institute and State University, 1988. http://hdl.handle.net/10919/53930.

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The study of the polymerization of alkyl vinyl ethers initiated by HI/I₂ catalyst is directed into two areas: the kinetics of the polymerization and the strategy of amine functionalized prepolymer synthesis. The polymerization reactions show living behavior in nonpolar solvents at low temperatures. The observed rate of polymerization under reaction conditions is linearly dependent on the initial concentration of hydrogen iodide and iodine, respectively. However, the monomer concentration does not influence the rate of polymerization(apparent zero-order). Two possible reaction schemes are proposed from the observed rate equation and attempts are made to distinguish them by using UV/visible spectroscopy and carbon-13 NMR spectroscopy. In both schemes a reversible interaction between a monomer and an iodine molecule is postulated as a necessary elemental reaction to fit the observed expression for the rate of polymerization. From spectroscopic analysis results, the interaction between the iodide compound(chain end) and the iodine molecule seems to be very weak compared to the interaction between the monomer and the iodine molecule. A synthetic strategy for amine functionalized prepolymer synthesis has been developed via a series of model reactions. Incorporation of a styrenic monomer at the propagating chain end of living poly(alkyl vinyl ethers) provides a convenient intermediate synthesis of a relatively stable amine functionalized prepolymer. Proper selection of substituents at the styrenic monomer optimizes the cross addition reaction and amination reactions. Linear alkylamines with lower carbon numbers are used in the amination reaction in order to promote the nucleophilic substitution reaction and to minimize possible elimination reactions. A series of amine functionalized oligomers are synthesized by employing the synthetic strategy in combination with the previous kinetic result of the homopolymerization. For oligomers, incorporation of a few units of ethyl vinyl ethers at the chain end facilitates the cross addition reaction. Synthesized amines are characterized by various spectroscopic methods. Then, titrated molecular weights show good agreement with their theoretical molecular weights in several cases.
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Chi, Jie. "Oxidation of Zeaxanthin and characterization of 3'-Alkyl Lutein ethers." FIU Digital Commons, 2001. http://digitalcommons.fiu.edu/etd/2161.

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One purpose of this study was to understand the oxidation metabolites of zeaxanthin, another was to prepare, purify, and characterize a series of 3'-alkyl lutein ethers for use as internal standards. Studies have proven that lutein and zeaxanthin are two of the principal carotenoids in human serum and the only carotenoids found in the retina, but their metabolism and transport in the human body are still only poorly understood. In vitro oxidation of zeaxanthin with MnO2 produced three components. They were characterized by HPLC, UV/Vis, MS, NMR and identified as all-trans rhodoxanthin and its cis-isomers. 3'-alkyl lutein ethers have been utilized as internal standards for carotenoid analysis in human serum and macular tissue. Nine 3'-alkyl lutein ethers were prepared by reaction of lutein with the corresponding acidified alcohols. The purified products were characterized by HPLC, UV/Vis, MS for the first time, and the resulting lutein ethers showed similar properties to lutein with increasing retention times as the alkyl chain lengthened. This provides us alternatives in selecting internal standards.
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Gillespie, Margaret Josephine. "Dichlorobenzyl alkyl ethers as standards in environmental analysis using gas chromatography." Thesis, University of Stirling, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.236048.

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Page, Jordan P. "Cobalt(II) Catalyzed Asymmetric Hydrovinylation of Alkyl- and Trialkylsilyloxy-1,3-Dienes." The Ohio State University, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=osu1357322022.

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Martin, Patricia. "Investigation of the synthesis and thermal rearrangements of 1,2,3,4,5-Pentaphenyl-2,4,-Cyclopentadiene Alkyl Ethers." Diss., Virginia Polytechnic Institute and State University, 1987. http://hdl.handle.net/10919/49858.

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A comparative synthetic study of a series of six 1,2,3,4,5-pentaphenyl-2,4-cyclopentadiene alkyl ethers was investigated. It was determined that the most efficient route to these ethers was not the most generally accepted route to ethers - the Williamson Reaction - but rather a solvolysis reaction between 1-bromo-1,2,3,4,5-pentaphenyl-2,4-cyclopentadiene and the appropriate alcohol. Thermal rearrangement of the ethers had been expected to rearrange by a [1,5]-sigmatropic shift of the phenyl group in the 1-position to yield the corresponding enol ether. However, this appeared to occur only as a trace in some cases. Rather, the major product of the thermal rearrangements of these ethers was actually the elimination product, the hydrocarbon, 1,2,3,4,5-pentaphenyl-2,4-cyclopentadiene. The elimination is most likely the result of a retro-ene reaction.
Ph. D.
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BECAERT, THIERRY. "Etudes pharmacologiques et electrophysiologiques in vitro et in vivo de o-alkyl ethers et de desoxy s-alkyl thioethers derives du glucose. Mise en evidence de proprietes antagonistes calciques." Amiens, 1990. http://www.theses.fr/1990AMIES022.

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L'etude de la toxicite de molecules tensioactives originales derivees du glucose a ete realisee chez la souris. Certains composes, les o-alkyl-3 et les desoxy-3 s-alkyl 1,2 ; d glucofurannose montrent des proprietes anesthesiques, myorelaxantes et anticonvulsivantes. In vitro, ces composes exercent un effet spasmolytique sur le duodenum de rat, suppriment l'activite cardiaque du cur de rat, et suppriment la contractilite du muscle squelettique (soleus) de souris. Une etude electrophysiologique realisee sur fibres musculaires et sur neurone d'ecrevisse montre que ces composes abolissent les potentiels d'action dependant du calcium et l'influx calcique transmembranaire. Etudies en condition de whole cell clamp sur myotubes de souris, ils bloquent les courants portes par les ions barium a travers les canaux calciques de types t et l
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Books on the topic "Ether(alkyl allyl)"

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. 1-ariruokishi-2,3-epokishipuropan: 1-allyloxy-2,3-epoxypropane. Tōkyō: Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Kanri Sentā, 2007.

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Elings, Jacob Antonius. Solid-acid catalysed reactions with epoxides and allyl aryl ethers. Delft, Netherlands: Delft University Press, 1997.

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Morales, Wilfredo. Analysis of a spacecraft instrument ball bearing assembly lubricated by a perfluoroalkylether. [Cleveland, Ohio: National Aeronautics and Space Administration, Lewis Research Center, 1986.

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Baumann, Wolfgang J. Platelet-Activating Factor and Structurally Related Alkyl Ether Lipids. Amer Oil Chemists Society, 1991.

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International Agency for Research on Cancer. and IARC Working Group on the Evaluation of the Carcinogenic Risk of Chemicals to Humans., eds. Allyl compounds, aldehydes, epoxides, and peroxides. [Lyon]: World Health Organization, International Agency for Research on Cancer, 1985.

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Aogain, Conor Fiacra Mac. The polymerization of alkyl vinyl ethers with ferricenium salts. 1987.

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Darsot, Mariam S. Anion chemistry of cyclic vinyl and allyl ethers: Structure and reactions. 1985.

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(Producer), WHO, ed. Vol 36 IARC Monographs: Allyl Compounds, Aldehydes, Epoxides and Peroxides (IARC Monographs on the Evaluation of Carcinogenic Risks to H). World Health Organisation, 1985.

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Book chapters on the topic "Ether(alkyl allyl)"

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Bährle-Rapp, Marina. "Steareth-10 Allyl Ether/Acrylates Copolymer." In Springer Lexikon Kosmetik und Körperpflege, 530. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_10018.

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Severance, Daniel L., and William L. Jorgensen. "Claisen Rearrangement of Allyl Vinyl Ether." In Structure and Reactivity in Aqueous Solution, 243–59. Washington, DC: American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0568.ch017.

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Carlsson, Ingemar, Adrian Harden, Stefan Lundmark, Ana Manea, Nicola Rehnberg, and Lennart Svensson. "Allyl Ethers in the Thiol-ene Reaction." In ACS Symposium Series, 65–75. Washington, DC: American Chemical Society, 2003. http://dx.doi.org/10.1021/bk-2003-0847.ch006.

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Sugiura, Takayuki, and Keizo Waku. "Composition of Alkyl Ether-Linked Phospholipids in Mammalian Tissues." In Platelet-Activating Factor and Related Lipid Mediators, 55–85. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-5284-6_4.

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Whitley, John W., Michael T. Burnette, Shellby C. Benefield, and Jason E. Bara. "Photopolymerization of Alkyl- and Ether-Functionalized Coordinated Ionic Liquid Monomers." In ACS Symposium Series, 69–82. Washington, DC: American Chemical Society, 2017. http://dx.doi.org/10.1021/bk-2017-1250.ch004.

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Plochocka, Krystyna, Xuejun Liu, Michael A. Tallon, and Osama M. Musa. "The Quintessential Alternating Copolymer Family: Alkyl Vinyl Ether co-Maleic Anhydride Copolymers." In Handbook of Maleic Anhydride Based Materials, 211–50. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-29454-4_4.

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Kim, Ha-Chul, Abdel M. El-Naggar, Garth L. Wilkes, Youngtai Yoo, and James E. McGrath. "Structure—Property Behavior of Caprolactone—Allyl Glycidyl Ether Copolymers Cross-Linked by Electron-Beam Irradiation." In ACS Symposium Series, 474–97. Washington, DC: American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0417.ch033.

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Höpken, J., S. Faulstich, and M. Möller. "Amphiphilic Allyl Ethers and Methacrylates Based on the Incompatibility of Fluorocarbon and Hydrocarbon Molecules." In Integration of Fundamental Polymer Science and Technology—5, 413–25. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3890-1_55.

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Franco, Delphine, Sandra Olivero, Jean-Paul Rolland, and Elisabet Dunach. "Nickel-catalyzed Electrochemical Reductive Cleavage of the Oxygen-Carbon Bond of Allyl Ethers: Synthetic Applications." In Novel Trends in Electroorganic Synthesis, 391–94. Tokyo: Springer Japan, 1998. http://dx.doi.org/10.1007/978-4-431-65924-2_118.

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Lux, H., D. T. Hart, P. J. Parker, and T. Klenner. "Ether Lipid Metabolism, GPI Anchor Biosynthesis, and Signal Transduction are Putative Targets for Anti-Leishmanial Alkyl Phospholipid Analogues." In Advances in Experimental Medicine and Biology, 201–11. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-0179-8_33.

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Conference papers on the topic "Ether(alkyl allyl)"

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Ge, Yingyong, Jingtao Hou, Zhichao Yang, Meijia Shi, and Yuanlong Zhang. "A study on toxicity and degradation of alkyl polyamin ether." In 2011 International Conference on Electrical and Control Engineering (ICECE). IEEE, 2011. http://dx.doi.org/10.1109/iceceng.2011.6058329.

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Grubbs II, G., Stewart Novick, S. Cooke, Daniel Obenchain, and Derek Frank. "CP-FTMW SPECTROSCOPY OF A CLAISEN REARRANGEMENT PRECURSOR ALLYL PHENYL ETHER." In 71st International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.mi02.

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Aoudia, M., R. S. Al-Maamari, M. Nabipoor, A. S. Al-Bemani, and S. Ayatollahi. "Novel Alkyl Ether Sulfonates for Improved Oil Recovery from Yibal Field (Oman)." In IOR 2007 - 14th European Symposium on Improved Oil Recovery. European Association of Geoscientists & Engineers, 2007. http://dx.doi.org/10.3997/2214-4609-pdb.24.a09.

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Cursaru, D. L., C. Tănăsescu, and V. Mărdărescu. "Effect of biodiesel and alkyl ether on diesel engine emissions and performances." In AIR POLLUTION 2011. Southampton, UK: WIT Press, 2011. http://dx.doi.org/10.2495/air110311.

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Hu, Yingmo. "The Surface Modification of Tourmaline Powder with Allyl Glycidyl Ether and Characterization." In The Joint Conferences of 2015 International Conference on Computer Science and Engineering Technology (CSET2015) and 2015 International Conference on Medical Science and Biological Engineering (MSBE2015). WORLD SCIENTIFIC, 2015. http://dx.doi.org/10.1142/9789814651011_0092.

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Jürgenson, G. Alvarez, C. Bittner, V. Kurkal-Siebert, G. Oetter, and J. Tinsley. "Alkyl Ether Carboxylate Surfactants for Chemically Enhanced Oil Recovery in Harsh Field Conditions." In SPE Asia Pacific Enhanced Oil Recovery Conference. Society of Petroleum Engineers, 2015. http://dx.doi.org/10.2118/174589-ms.

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Brandl, Andreas. "Study of Acrylic Acid-co-Polyethylene Glycol Allyl Ether as Cement Retarder Over a Broad Temperature Range." In IADC/SPE Asia Pacific Drilling Technology Conference. Society of Petroleum Engineers, 2016. http://dx.doi.org/10.2118/180675-ms.

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Frank, Derek, G. Grubbs II, S. Cooke, Stewart Novick, Wei Lin, and Daniel Obenchain. "MONITORING THE REACTION PRODUCTS OF PERFLUOROPROPIONIC ACID AND ALLYL PHENYL ETHER USING CHIRPED-PULSE FOURIER TRANSFORM MICROWAVE (CP-FTMW) SPECTROSCOPY." In 69th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.fd01.

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Geraskina, Evgeniya V., Alexey A. Moikin, and Ludmila L. Semenycheva. "The thickening additives for mineral and synthetic oils based on the copolymers of alkyl acrylates or methacrylates and butyl vinyl ether." In TIMES OF POLYMERS (TOP) AND COMPOSITES 2014: Proceedings of the 7th International Conference on Times of Polymers (TOP) and Composites. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4876905.

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Purdon, A. D., and J. B. Smith. "RELEASE AND TRANSACYLATION OF ARACHIDONATE FROM A COMMON POOL OF 1-ACYL-2-ARACHIDONOYL GLYCEROPHOSPHOCHOLINE IN HUMAN PLATELETS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643391.

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Abstract:
We have previously shown that the main source of arachidonate in thrombin-stimulated human platelets is 1-acyl-2-arachidonoyl (AA) glycerophosphocholine (GPC) and release of 3H-AA from this phospholipid also was correlated with increased 3H-AA in ether phospholipid. This ATP independent transfer of 3H-AA from 1,2 diacyl GPC to ether phospholipid (transacylation) also occurs in resting cells. Human platelets in 1/10 volume of plasma (ACD anticoagulant, pH 6.5) were radiolabelled with 3H-AA for 60 min at 37°C and then exogenous 3H-AA was removed by gel filtration into Tyrode's buffer, pH 7.4, 0.2% albumin. These radiolabelled cells were incubated in the absence of exogenous 3H-AA for four hours followed by Bligh and Dyer extraction and thin layer chromatography purification of phospholipids. 3H-AA in 1,2 diacyl GPC was found to decrease by over 20% and increase substantially in 1-0-alkyl-2-acyl GPC and 1-0-alk-1'-enyl-2-acyl glycerophospho ethanolamine (GPE), In this same time interval the mass of AA released by thrombin (5 U/ml, 10 min, 37°C, no stirring)in the presence of BIT 775C and measured by GLC, stayed the same (30 nmoles/109 cells), however, the specific activity decreased. Using reverse phase HPLC to resolve diradylglycerobenzoate derivatives of phospholipids: acylation, deacylation, and transacylation were observed for individual AA-containing molecular species of phospholipid, including those with an unsaturated fatty acid at sn-1. In particular the radiolabellinq of the 1-unsaturate-2-arachidonoyl GPC correlated with the specific activity of the 3H-AA released by stimulation with thrombin. Furthermore, 1-arachidonoyl-2-3H-arachidonoyl GPC was completely deacylated while 50 % of its mass remained. This contrasted with 16:0, and 18:0-2-arachidonoyl GPC in which the specific activity remained the same before and after deacylation. We conclude that deacylation of AA-containing molecular species of 1,2 diacyl GPC in stimulated cells includes molecular species which are also a source of arachidonic acid for transacylation reactions.
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Reports on the topic "Ether(alkyl allyl)"

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Percec, V., Q. Zheng, and M. Lee. Molecular Engineering of Liquid Crystal Polymers by Living Polymerization. 13. Synthesis and Living Cationic Polymerization of 4-((S(-)-2- Methyl-1-Butyl)Oxycarbonyl)-4'-(omega-Oxyalkyl-1-Vinyl Ether)Biphenyl with Undecanyl and Hexyl Alkyl Groups. Fort Belvoir, VA: Defense Technical Information Center, April 1991. http://dx.doi.org/10.21236/ada235791.

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NIOSH skin notation (SK) profiles: allyl glycidyl ether (AGE) [CAS No. 106-92-3]. U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, August 2014. http://dx.doi.org/10.26616/nioshpub2014143.

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