Статті в журналах з теми "Ethynyl ketone"
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Yavari, Issa, Abdolali Alizadeh, and Mohammad Anary-Abbasinejad. "Stable 1,3-Diionic Organophosphorus Compounds Derived from Ethynyl Phenyl Ketone." Phosphorus, Sulfur, and Silicon and the Related Elements 177, no. 1 (January 1, 2002): 81–86. http://dx.doi.org/10.1080/10426500210236.
Повний текст джерелаSun, Yin-wei, Qin Xu, and Min Shi. "Gold-catalyzed reaction of oxabicyclic alkenes with electron-deficient terminal alkynes to produce acrylate derivatives." Beilstein Journal of Organic Chemistry 9 (October 1, 2013): 1969–76. http://dx.doi.org/10.3762/bjoc.9.233.
Повний текст джерелаWilbur, J. M., and B. A. Bonner. "Synthesis of hydrogen-terminated aliphatic bis(ethynyl ketone)s and aliphatic poly(enamine-ketone)s and poly(enonesulfide)s." Journal of Polymer Science Part A: Polymer Chemistry 28, no. 13 (December 1990): 3747–59. http://dx.doi.org/10.1002/pola.1990.080281318.
Повний текст джерелаTIWARI, R. K., A. K. SAXENA, and P. S. VENKATARAMANI. "ChemInform Abstract: Nucleophilic Addition to Aryl Ethynyl Ketone: Addition of Oxygen Containing Nucleophiles to Terephthaloyl Acetylene." ChemInform 28, no. 13 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199713065.
Повний текст джерелаYavari, Issa, Mohammad Anary-Abbasinejad, and Abdolali Alizadeh. "On the Reaction between Alkyl Isocyanides and Ethynyl Phenyl Ketone in the Presence of N,N′-Dimethylbarbituric Acid." Monatshefte f?r Chemie / Chemical Monthly 133, no. 9 (September 1, 2002): 1221–24. http://dx.doi.org/10.1007/s007060200093.
Повний текст джерелаHe, QinZheng, JinYan Wang, LiShuai Zong, Rui Liu, and XiGao Jian. "Soluble and crosslinkable poly(phthalazinone ether ketone)s with pendent terminal ethynyl groups: synthesis, characterization and click modification." Polymer International 64, no. 7 (January 12, 2015): 875–83. http://dx.doi.org/10.1002/pi.4860.
Повний текст джерелаYavari, Issa, Mohammad Anary-Abbasinejad, and Abdolali Alizadeh. "On the Reaction Between Alkyl Isocyanides and Ethynyl Phenyl Ketone in the Presence of N,N′-Dimethylbarbituric Acid." ChemInform 34, no. 1 (January 7, 2003): no. http://dx.doi.org/10.1002/chin.200301154.
Повний текст джерелаLee, Hyung-Jong, Myung-Hyun Lee, Min-Cheol Oh, Joo-Heon Ahn, and Seon Gyu Han. "Crosslinkable polymers for optical waveguide devices. II. Fluorinated ether ketone oligomers bearing ethynyl group at the chain end." Journal of Polymer Science Part A: Polymer Chemistry 37, no. 14 (July 15, 1999): 2355–61. http://dx.doi.org/10.1002/(sici)1099-0518(19990715)37:14<2355::aid-pola9>3.0.co;2-9.
Повний текст джерелаMukaiyama, Teruaki, Shigekazu Matsui, Koichi Homma, and Sh\={u} Kobayashi. "Regioselective Condensation of Ethynyl Vinyl Ketone or 2-Propynyl Ether Derivatives with Silyl Enol Ethers Catalyzed by Trityl Perchlorate." Bulletin of the Chemical Society of Japan 63, no. 9 (September 1990): 2687–90. http://dx.doi.org/10.1246/bcsj.63.2687.
Повний текст джерелаMUKAIYAMA, T., S. MATSUI, K. HOMMA, and S. KOBAYASHI. "ChemInform Abstract: Regioselective Condensation of Ethynyl Vinyl Ketone or 2-Propynyl Ether Derivatives with Silyl Enol Ethers Catalyzed by Trityl Perchlorate." ChemInform 22, no. 4 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199104110.
Повний текст джерелаGiridhar Reddy, P., K. Ramesh, S. Shylaja, K. C. Rajanna, and S. Kandlikar. "Ru (III) Catalyzed Oxidation of Aliphatic Ketones by N-Bromosuccinimide in Aqueous Acetic Acid: A Kinetic Study." Scientific World Journal 2012 (2012): 1–7. http://dx.doi.org/10.1100/2012/456516.
Повний текст джерелаLiu, Hsing-Jang, Waiseng Martin Feng, Jeung Bea Kim, and Eric N. C. Browne. "Lewis acid catalyzed Diels–Alder reactions of two useful dienyl phosphate esters." Canadian Journal of Chemistry 72, no. 10 (October 1, 1994): 2163–75. http://dx.doi.org/10.1139/v94-275.
Повний текст джерелаChen, Chan Cheng, Tsung Han Han, Sheng Xiang Hong, and Der Jen Hsu. "Auto-Ignition Temperature Data for Selected Ketones." Advanced Materials Research 560-561 (August 2012): 145–51. http://dx.doi.org/10.4028/www.scientific.net/amr.560-561.145.
Повний текст джерелаStephenson, W. Kirk, and Richard Fuchs. "Enthalpies of interaction of ketones with organic solvents." Canadian Journal of Chemistry 63, no. 2 (February 1, 1985): 336–41. http://dx.doi.org/10.1139/v85-057.
Повний текст джерелаNakatani, Kazuhiko, Akimitsu Okamoto, Mikito Yamanuki, and Isao Saito. "Highly Efficient Synthesis of 2-Substituted 4H-Chromen-4-ones by means of F--Induced 6-Endo-Digonal Cyclization of o-(Silyloxy)phenyl Ethynyl Ketone Derivatives." Journal of Organic Chemistry 59, no. 16 (August 1994): 4360–61. http://dx.doi.org/10.1021/jo00095a003.
Повний текст джерелаSivak, Jacob G., Kelley L. Herbert, and Anne L. Baczmanski. "The Use of the Cultured Bovine Lens to Measure the In Vitro Ocular Irritancy of Ketones and Acetates." Alternatives to Laboratory Animals 23, no. 5 (September 1995): 689–98. http://dx.doi.org/10.1177/026119299502300522.
Повний текст джерелаNAKATANI, K., A. OKAMOTO, M. YAMANUKI, and I. SAITO. "ChemInform Abstract: Highly Efficient Synthesis of 2-Substituted 4H-Chromen-4-ones by Means of F--Induced 6-endo-digonal Cyclization of o-(Silyloxy)phenyl Ethynyl Ketone Derivatives." ChemInform 26, no. 6 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199506150.
Повний текст джерелаAndraos, J., Y. Chiang, S. J. Eustace, A. J. Kresge, S. W. Paine, V. V. Popik, and K. Sung. "Article." Canadian Journal of Chemistry 77, no. 4 (April 1, 1999): 459–62. http://dx.doi.org/10.1139/v99-058.
Повний текст джерелаSommariva, R., J. A. de Gouw, M. Trainer, E. Atlas, P. D. Goldan, W. C. Kuster, C. Warneke, and F. C. Fehsenfeld. "Emissions and photochemistry of oxygenated VOCs in urban plumes in the Northeastern United States." Atmospheric Chemistry and Physics Discussions 8, no. 3 (June 30, 2008): 12371–408. http://dx.doi.org/10.5194/acpd-8-12371-2008.
Повний текст джерелаSommariva, R., J. A. de Gouw, M. Trainer, E. Atlas, P. D. Goldan, W. C. Kuster, C. Warneke, and F. C. Fehsenfeld. "Emissions and photochemistry of oxygenated VOCs in urban plumes in the Northeastern United States." Atmospheric Chemistry and Physics 11, no. 14 (July 21, 2011): 7081–96. http://dx.doi.org/10.5194/acp-11-7081-2011.
Повний текст джерелаPark, Hoey Kyung, June-shu Ahn, and Jungho Cho. "Simulation Study of Methyl ethyl ketone-Cyclohexane Azeotrope on the Pressure-Swing Distillation." Journal of the Korea Academia-Industrial cooperation Society 17, no. 3 (March 31, 2016): 708–15. http://dx.doi.org/10.5762/kais.2016.17.3.708.
Повний текст джерелаMaGee, David I., Mahesh Ramaseshan, and James D. Leach. "Synthesis of cyclic and acyclic imides, sulfonimides, and N-carbobenzyloxyamides by ketene trapping." Canadian Journal of Chemistry 73, no. 12 (December 1, 1995): 2111–18. http://dx.doi.org/10.1139/v95-260.
Повний текст джерелаChun, Stephanie W., та Alison R. H. Narayan. "Biocatalytic Synthesis of α-Amino Ketones". Synlett 30, № 11 (19 березня 2019): 1269–74. http://dx.doi.org/10.1055/s-0037-1611755.
Повний текст джерелаKam, Sang-Kyu, Jin-Woo Jeon, and Min-Gyu Lee. "Effect of Methyl Ethyl Ketone and Ethyl Acetate Vapor on Photocatalytic Decomposition of n-Pentane Vapor." Journal of Environmental Science International 23, no. 6 (June 30, 2014): 1151–56. http://dx.doi.org/10.5322/jesi.2014.23.6.1151.
Повний текст джерелаAl-Auda, Zahraa, Hayder Al-Atabi, and Keith Hohn. "Metals on ZrO2: Catalysts for the Aldol Condensation of Methyl Ethyl Ketone (MEK) to C8 Ketones." Catalysts 8, no. 12 (December 5, 2018): 622. http://dx.doi.org/10.3390/catal8120622.
Повний текст джерелаPenner, Glenn H. "Conformational preference and internal rotation about the C1—Cα bond in phenylacetaldehyde and some benzyl alkyl ketones from 1H nuclear magnetic resonance and abinitio molecular orbital calculations". Canadian Journal of Chemistry 65, № 3 (1 березня 1987): 538–40. http://dx.doi.org/10.1139/v87-094.
Повний текст джерелаSuggs, J. William, and Chul-Ho Jun. "Metal-catalysed alkyl ketone to ethyl ketone conversions in chelating ketones via carbon–carbon bond cleavage." J. Chem. Soc., Chem. Commun., no. 2 (1985): 92–93. http://dx.doi.org/10.1039/c39850000092.
Повний текст джерелаYamabe, Shinichi, Guixiang Zeng, Wei Guan, and Shigeyoshi Sakaki. "Substrate dependent reaction channels of the Wolff–Kishner reduction reaction: A theoretical study." Beilstein Journal of Organic Chemistry 10 (January 23, 2014): 259–70. http://dx.doi.org/10.3762/bjoc.10.21.
Повний текст джерелаL. Morgan, Sandra M. Ward, Ralph E., Daniel. "INHALATION TOXICITY STUDIES OF THE α,β-UNSATURATED KETONES: Ethyl Vinyl Ketone". Inhalation Toxicology 13, № 8 (січень 2001): 633–58. http://dx.doi.org/10.1080/08958370126864.
Повний текст джерелаMorgan, Daniel L., Sandra M. Ward, Ralph E. Wilson, Herman C. Price, Robert W. O'Connor, John C. Seely та Michael L. Cunningham. "INHALATION TOXICITY STUDIES OF THE α,β-UNSATURATED KETONES: Ethyl Vinyl Ketone". Inhalation Toxicology 13, № 8 (1 серпня 2001): 633–58. http://dx.doi.org/10.1080/08958370152409883.
Повний текст джерелаŠindelář, Karel, Jiří Holubek, Oluše Matoušová, Emil Svátek, Martin Valchář, Antonín Dlabač, Nataša Dlohožková, Marta Hrubantová, and Miroslav Protiva. "Aminoalkylidene and aminoalkyl derivatives of 6,11-dihydrodibenzo[b,e]thiepin-2- and -9-carbonitrile and 4,10-dihydrothieno[2,3-c]-1-benzothiepin-6-carbonitrile; Antidepressants with a new activity profile." Collection of Czechoslovak Chemical Communications 53, no. 2 (1988): 340–60. http://dx.doi.org/10.1135/cccc19880340.
Повний текст джерелаBonilla-Landa, Israel, Emizael López-Hernández, Felipe Barrera-Méndez, Nadia C. Salas, and José L. Olivares-Romero. "Hafnium(IV) Chloride Catalyzes Highly Efficient Acetalization of Carbonyl Compounds." Current Organic Synthesis 16, no. 6 (November 26, 2019): 913–20. http://dx.doi.org/10.2174/1570179416666190715100505.
Повний текст джерелаZhuchkov, V. I., S. L. Nazansky, O. N. Krupinova, and A. K. Frolkova. "VAPOUR-LIQUID EQUILIBRIUM IN SYSTEMS WITH ISOBUTYL ACETATE, ACETIC ACID AND METHYL ETHYL KETONE." Fine Chemical Technologies 11, no. 2 (April 28, 2016): 38–45. http://dx.doi.org/10.32362/2410-6593-2016-11-2-38-45.
Повний текст джерелаDransfield, R. D., R. Brightwell, M. F. Chaudhury, T. K. Golder, and S. A. R. Tarimo. "The use of odour attractants for sampling Glossina pallidipes Austen(Diptera: Glossinidae) at Nguruman, Kenya." Bulletin of Entomological Research 76, no. 4 (December 1986): 607–19. http://dx.doi.org/10.1017/s000748530001511x.
Повний текст джерелаGlowacz-Czerwonka, Dorota. "Oligoetherols with S-Trazine Ring Based on Hydroxymethyl Derivatives of Methyl Ethyl Ketone." Chemistry & Chemical Technology 11, no. 1 (March 15, 2017): 45–48. http://dx.doi.org/10.23939/chcht11.01.045.
Повний текст джерелаLiu, Baoxiang, Yang Yang, Likun Ren, Zhengbo Su, Xin Bian, Jing Fan, Yuanyuan Wang, Bing Han, and Na Zhang. "HS-GC-IMS and PCA to Characterize the Volatile Flavor Compounds in Three Sweet Cherry Cultivars and Their Wines in China." Molecules 27, no. 24 (December 19, 2022): 9056. http://dx.doi.org/10.3390/molecules27249056.
Повний текст джерелаYoung, Jay A. "Methyl Ethyl Ketone." Journal of Chemical Education 81, no. 5 (May 2004): 630. http://dx.doi.org/10.1021/ed081p630.
Повний текст джерелаLuttrell, William E., and Lauren R. Bellcock. "Methyl ethyl ketone." Journal of Chemical Health and Safety 22, no. 4 (July 2015): 33–36. http://dx.doi.org/10.1016/j.jchas.2015.06.007.
Повний текст джерелаKurbatova, Marina, Mariya Cherencova, Tat'yana Raskulova, Mihail Fereferov, and Aleksey Ryabcov. "LOW TEMPERATURE DEWAXING OF OILS IN PRESENCE INDIVIDUAL SOLVENT." Bulletin of the Angarsk State Technical University 1, no. 12 (December 18, 2018): 69–72. http://dx.doi.org/10.36629/2686-777x-2018-1-12-69-72.
Повний текст джерелаRaskulova, Tat'yana, Mihail Fereferov, Marina Kurbatova, Mariya Cherencova, and Irina Polyak. "ON THE REPLACE ABILITY OF SOLVENT IN THE PROCESS OF LOW TEMPERATURE DE-WAXING OF OILS." Modern Technologies and Scientific and Technological Progress 2018, no. 1 (March 23, 2020): 38–39. http://dx.doi.org/10.36629/2686-9896-2020-2018-1-38-39.
Повний текст джерелаAlcoberro, Sandra, Alejandro Gómez-Palomino, Ricard Solà, Pedro Romea, Fèlix Urpí, and Mercè Font-Bardia. "Stereoselective Titanium-Mediated Aldol Reactions of a Chiral Lactate-Derived Ethyl Ketone with Ketones." Organic Letters 16, no. 2 (December 27, 2013): 584–87. http://dx.doi.org/10.1021/ol403461b.
Повний текст джерелаCollins, DJ, JD Cullen, and GM Stone. "The Structure and Function of Estrogens .10. Synthesis of 5,5-Dimethyl-Cis-4b,5,6,10b,11,12-Hexahydrochrysene-2,8-Diol - the Estrogenic Activity of This and of Related C-Methylated Hydrochrysenediols." Australian Journal of Chemistry 41, no. 5 (1988): 745. http://dx.doi.org/10.1071/ch9880745.
Повний текст джерелаTang, Fei-Fei, Wu-Lin Yang, Xingxin Yu, and Wei-Ping Deng. "Cu(OAc)2/FOXAP complex catalyzed construction of 2,5-dihydropyrrole derivatives via asymmetric 1,3-dipolar cycloaddition of azomethine ylides to ethynyl ketones." Catalysis Science & Technology 5, no. 7 (2015): 3568–75. http://dx.doi.org/10.1039/c5cy00422e.
Повний текст джерелаK. Amin, Bassam. "Comparative Study of Marginal Gap Among Zirconium Dioxide, Poly Ethyl Ethyl Ketone and Porcelain Fused to Metal Implant Supported Crowns." Sulaimani dental journal 6, no. 1 (June 20, 2019): 29–32. http://dx.doi.org/10.17656/sdj.10087.
Повний текст джерелаJörges, Mike, Felix Krischer, and Viktoria H. Gessner. "Transition metal–free ketene formation from carbon monoxide through isolable ketenyl anions." Science 378, no. 6626 (December 23, 2022): 1331–36. http://dx.doi.org/10.1126/science.ade4563.
Повний текст джерелаÖzmen, Dilek. "(Liquid+liquid) equilibria of (water+propionic acid+methyl isoamyl ketone or diisobutyl ketone or ethyl isoamyl keton) at T=298.2K." Fluid Phase Equilibria 250, no. 1-2 (December 2006): 70–75. http://dx.doi.org/10.1016/j.fluid.2006.10.004.
Повний текст джерелаHou, Jia Qi, Ming Xiao Li, Zi Min Wei, Bei Dou Xi, Xuan Jia, Chao Wei Zhu, and Dong Ming Liu. "Critical Components of Odors and VOCs in Mechanical Biological Treatment Process of MSW." Advanced Materials Research 647 (January 2013): 438–49. http://dx.doi.org/10.4028/www.scientific.net/amr.647.438.
Повний текст джерелаFockenberg, Christopher. "Product Study of the Photolysis of Ketene and Ethyl Ethynyl Ether at 193.3 nm." Journal of Physical Chemistry A 109, no. 32 (August 2005): 7140–50. http://dx.doi.org/10.1021/jp044092g.
Повний текст джерелаOnaca, Christina, Martin Kieninger, Karl-H. Engesser, and Josef Altenbuchner. "Degradation of Alkyl Methyl Ketones by Pseudomonas veronii MEK700." Journal of Bacteriology 189, no. 10 (March 9, 2007): 3759–67. http://dx.doi.org/10.1128/jb.01279-06.
Повний текст джерелаSkornyakov, Yu V., N. A. Lozinskaya, M. V. Proskurnina, and N. S. Zefirov. "New Synthesis of Conjugated Ethynyl Vinyl Ketones." Russian Journal of Organic Chemistry 41, no. 4 (April 2005): 617. http://dx.doi.org/10.1007/s11178-005-0213-z.
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