Relevant bibliographies by topics / Ketoether

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  2. Dissertations / Theses

Academic literature on the topic 'Ketoether'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 April 2022

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Journal articles on the topic "Ketoether"

1

Groß, Tobias, and Peter Metz. "An Efficient Gold-Catalyzed Domino Process for the Construction of Tetracyclic Ketoethers." Chemistry - A European Journal 19, no. 44 (October 2, 2013): 14787–90. http://dx.doi.org/10.1002/chem.201302985.

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Gross, Tobias, and Peter Metz. "ChemInform Abstract: An Efficient Gold-Catalyzed Domino Process for the Construction of Tetracyclic Ketoethers." ChemInform 45, no. 13 (March 14, 2014): no. http://dx.doi.org/10.1002/chin.201413031.

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Gibilisco, Rodrigo Gastón, Ian Barnes, Iustinian Gabriel Bejan, and Peter Wiesen. "Atmospheric fate of two relevant unsaturated ketoethers: kinetics, products and mechanisms for the reaction of hydroxyl radicals with (<i>E</i>)-4-methoxy-3-buten-2-one and (1<i>E</i>)-1-methoxy-2-methyl-1-penten-3-one." Atmospheric Chemistry and Physics 20, no. 14 (July 29, 2020): 8939–51. http://dx.doi.org/10.5194/acp-20-8939-2020.

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Abstract. The kinetics of the gas phase reactions of hydroxyl radicals with two unsaturated ketoethers (UKEs) at (298±3) K and 1 atm of synthetic air have been studied for the first time using the relative-rate technique in an environmental reaction chamber by in situ Fourier-transform infrared spectroscopy (FTIR). The rate coefficients obtained using propene and isobutene as reference compounds were (in units of 10−10 cm3 molecule−1 s−1) as follows: kTMBO (OH + (E)-4-methoxy-3-buten-2-one) = (1.41±0.11) and kMMPO (OH + (1E)-1-methoxy-2-methyl-1-penten-3-one) = (3.34±0.43). In addition, quantification of the main oxidation products in the presence of NOx has been performed, and degradation mechanisms for these reactions were developed. Methyl formate, methyl glyoxal, peroxyacetyl nitrate (PAN) and peroxypropionyl nitrate (PPN) were identified as main reaction products and quantified for both reactions. The results of the present study provide new insights regarding the contribution of these multifunctional volatile organic compounds (VOCs) in the generation of secondary organic aerosols (SOAs) and long-lived nitrogen containing compounds in the atmosphere. Atmospheric lifetimes and implications are discussed in light of the obtained results.
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Oku, Akira, Shigeji Ohki, Tomohiro Yoshida, and Kenji Kimura. "Three-carbon ring-enlargement of ethereal oxonium ylides—a viable synthesis of medium-sized cyclic ketoethers." Chem. Commun., no. 9 (1996): 1077–78. http://dx.doi.org/10.1039/cc9960001077.

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Pflieger, P., C. Mioskowski, J. P. Salaun, D. Weissbart, and F. Durst. "A new synthesis of α-ketoethers via anchimerically assisted substitution of an α-sulfinyl function with alcohols." Tetrahedron Letters 30, no. 21 (January 1989): 2791–94. http://dx.doi.org/10.1016/s0040-4039(00)99126-3.

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6

Erol, Ibrahim, Cengiz Soykan, Zülfiye Ilter, and Misir Ahmedzade. "Thermal degradation of poly 2-[3-(6-tetralino)-3-methylcyclobutyl]-2-ketoethyl methacrylate." Polymer Degradation and Stability 81, no. 2 (January 2003): 287–95. http://dx.doi.org/10.1016/s0141-3910(03)00099-5.

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OKU, A., S. OHKI, T. YOSHIDA, and K. KIMURA. "ChemInform Abstract: Three-Carbon Ring-Enlargement of Ethereal Oxonium Ylides. A Viable Synthesis of Medium-Sized Cyclic Ketoethers." ChemInform 27, no. 37 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199637225.

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8

Kevill, Dennis N., and Chang-Bae Kim. "Correlation of the Rates of Solvolysis of 2-Phenyl-2-ketoethyl Bromide and Tosylate." Journal of Organic Chemistry 70, no. 4 (February 2005): 1490–93. http://dx.doi.org/10.1021/jo048103d.

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Erol, Ibrahim, Zulfiye Ilter, Mehmet Coskun, and Misir Ahmedzade. "Synthesis and characterization of two new aryl cyclobutyl ketoethyl methacrylate monomers and their polymers." Journal of Polymer Science Part A: Polymer Chemistry 39, no. 23 (2001): 4167–73. http://dx.doi.org/10.1002/pola.10068.

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Ding, Lei, Qinxiong He, and Jianping Deng. "Using hydroxypropyl-β-cyclodextrin for the preparation of hydrophobic poly(ketoethyl methacrylate) in aqueous medium." Journal of Applied Polymer Science 115, no. 5 (October 26, 2009): 2933–39. http://dx.doi.org/10.1002/app.31390.

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Dissertations / Theses on the topic "Ketoether"

1

Tougani, Rajaallah Amina. "Acylation d'énolates lithiens d'esters et d'organozinciques allyliques : obtention de composés carbonyles fonctionnels et utilisation de ces derniers à la synthèse d'hétérocycles oxygénés à cinq chainons." Paris 6, 1986. http://www.theses.fr/1986PA066522.

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Estel, Lionel. "Fonctionnalisation d'aminopyridines par métallation : application à la synthèse d'hétérocycles." Rouen, 1988. http://www.theses.fr/1988ROUES035.

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L'action d'aldéhydes aromatiques sur des pivalolaminopyridines ortho lithiées a donné des alcools secondaires qui ont été oxydés en cétones. Ceci permettant une synthèse en 4 étapes des amino-2 pyridyl-3, amino-3 pyridyl-4 et amino-4 pyridyl-3 arylméthanones. De la même façon, la fluoro-4 lithio-3 pyridine conduit à l'amino-4 pyridyl-3 phénylméthanone. Pour montrer l'intérêt de la méthode, des pyridopyrimidinones et des benzonaphtyridines ont été synthétisées. Par ailleurs, la fluoro-2 pyridine métallée, réagit avec l'iode pour donner des iodo-3 pyridines diversement substituées en 2. Une synthèse en 2 étapes des ortho iodo aminopyridines a été développée à partir des trois monoaminopyridines. La substitution de l'iode par des énolates dans les conditions de la SNR1 conduit après cyclisation acide aux aza-5, -6 et -7 indoles substitués en 2. Enfin, des aza-5 indoles disubstitués en -2, -3 ont été obtenus par action d'alphaméthoxycétones sur la lithio-3 pivalamido-4 pyridine et cyclisation acide
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Haelters, Jean-Pierre. "Synthèse de dérivés phosphono-indoliques-benzofuranniques et -pyrroliques à partir d'hydrazones phosphonates." Brest, 1987. http://www.theses.fr/1987BRES2002.

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Des derives phosphonoindoliques sont prepares par cyclisation d'arylhydrazones d'oxoalkylphosphonates selon fisher et par cyclodeshydratation d'arylamino-1 et arylamino-3 oxo-2 propylphosphonates selon bischler. Des indolyl-2 et indolyl-3 phosphonates, des indolylmethyl-2 et des indolylmethyl-3 phosphonates diversement substitues et leurs acides phosphoniques correspondants sont decrits. Toutes structures sont analysees par rmn **(1)h, **(31)p et 1**(3)c. L'analogue phosphore de l'intermediaire a aussi ete prepare. L'extention de la reaction de bischler aux aryloxycetones permet d'atteindre des benzofuryl-2 phosphonate et de benzofurylmethyl-3 phosphonates. Deux nouveaux reactifs sont utilises pour acceder aux arylaminocetones et aux aryloxycetones : les chloro-1 et chloro-3 methoxycarbonylhydrazono-2 propyl-phosphonates de diethyle, composes qui, traites en milieu basique, donnent des azoenes qui additionnent les anilines et les phenols. Ces azoenes additionnent aussi les carbanions, notamment les carbanions derives de cetones pour conduire, apres hydrolyse soit a des derives du pyrrole, soit a des dioxy-2, -5-alkylphosphonates precurseurs de cyclopentenones selon wittig-horner
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