Artículos de revistas sobre el tema "Ethers"
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Kim, Yong-Hak y Karl-Heinrich Engesser. "Degradation of Alkyl Ethers, Aralkyl Ethers, and Dibenzyl Ether by Rhodococcus sp. Strain DEE5151, Isolated from Diethyl Ether-Containing Enrichment Cultures". Applied and Environmental Microbiology 70, n.º 7 (julio de 2004): 4398–401. http://dx.doi.org/10.1128/aem.70.7.4398-4401.2004.
Texto completoZmysłowski, Adam, Jerzy Sitkowski, Katarzyna Bus, Katarzyna Michalska y Arkadiusz Szterk. "Synthesis of Oxidized 3β,3′β-Disteryl Ethers and Search after High-Temperature Treatment of Sterol-Rich Samples". International Journal of Molecular Sciences 22, n.º 19 (27 de septiembre de 2021): 10421. http://dx.doi.org/10.3390/ijms221910421.
Texto completoDachavaram, Soma Shekar, Narsimha R. Penthala, Julie L. Calahan, Eric J. Munson y Peter A. Crooks. "Highly sulphated cellulose: a versatile, reusable and selective desilylating agent for deprotection of alcoholic TBDMS ethers". Organic & Biomolecular Chemistry 16, n.º 33 (2018): 6057–62. http://dx.doi.org/10.1039/c8ob01438h.
Texto completoPalanychamy, Prakas, Steven Lim, Yeow Hong Yap y Loong Kong Leong. "Critical Review of the Various Reaction Mechanisms for Glycerol Etherification". Catalysts 12, n.º 11 (21 de noviembre de 2022): 1487. http://dx.doi.org/10.3390/catal12111487.
Texto completoModrzakowski, Malcolm C. y William R. Finnerty. "Intermediary metabolism of Acinetobacter grown on dialkyl ethers". Canadian Journal of Microbiology 35, n.º 11 (1 de noviembre de 1989): 1031–36. http://dx.doi.org/10.1139/m89-171.
Texto completoRagauskas, Arthur J. y J. B. Stothers. "13C magnetic resonance studies. 120. The Simmons–Smith reaction with some silyl enol ethers. Unusual ring expansions of some norcamphorsti". Canadian Journal of Chemistry 63, n.º 11 (1 de noviembre de 1985): 2969–74. http://dx.doi.org/10.1139/v85-492.
Texto completoSireesha, Reddymasu, Reddymasu Sreenivasulu, Choragudi Chandrasekhar y Mannam Subba Rao. "A Facile, Efficient and Selective Deprotection of P - Methoxy Benzyl Ethers Using Zinc (II) Trifluoromethanesulfonate". Letters in Organic Chemistry 16, n.º 12 (9 de octubre de 2019): 955–58. http://dx.doi.org/10.2174/1570178616666190222151934.
Texto completoMireles, Raul, Joaquin Ramirez-Ramirez, Miguel Alcalde y Marcela Ayala. "Ether Oxidation by an Evolved Fungal Heme-Peroxygenase: Insights into Substrate Recognition and Reactivity". Journal of Fungi 7, n.º 8 (28 de julio de 2021): 608. http://dx.doi.org/10.3390/jof7080608.
Texto completoGhosh, Arun, Anthony Tomaine y Kelsey Cantwell. "Lewis Acid Mediated Cyclizations: Diastereoselective Synthesis of Six- to Eight-Membered Substituted Cyclic Ethers". Synthesis 49, n.º 18 (25 de julio de 2017): 4229–46. http://dx.doi.org/10.1055/s-0036-1589054.
Texto completoVerevkin, Sergey P. y Aleksandra A. Zhabina. "Platform Chemicals from Ethylene Glycol and Isobutene: Thermodynamics “Pays” for Biomass Valorisation and Acquires “Cashback”". Chemistry 5, n.º 2 (9 de mayo de 2023): 1171–89. http://dx.doi.org/10.3390/chemistry5020079.
Texto completoIranpoor, Nasser, Habib Firouzabadi y Mohammad Gholinejad. "4-Aminophenyldiphenylphosphinite (APDPP), a new heterogeneous and acid scavenger phosphinite — Conversion of alcohols, trimethylsilyl, and tetrahydropyranyl ethers to alkyl halides with halogens or N-halosuccinimides". Canadian Journal of Chemistry 84, n.º 7 (1 de julio de 2006): 1006–12. http://dx.doi.org/10.1139/v06-120.
Texto completoNavarro, Jaume. "Killed by its own obituaries: Explaining the demise of the ether". Science in Context 34, n.º 2 (junio de 2021): 209–25. http://dx.doi.org/10.1017/s0269889722000175.
Texto completoHajko, J., G. Szabovik, J. Kerekgyarto, M. Kajtar y A. Liptak. "Hydrogenolysis of the 4,6-O-Ketals of Glucopyranosides. Configuration-Dependent High Regio- and Stereo-Selectivity of the Diastereoisomeric Acetophenone Derivatives". Australian Journal of Chemistry 49, n.º 3 (1996): 357. http://dx.doi.org/10.1071/ch9960357.
Texto completoAndersen, F. Alan. "Special Report: Reproductive and Developmental Toxicity of Ethylene Glycol and Its Ethers". International Journal of Toxicology 18, n.º 2_suppl (marzo de 1999): 53–67. http://dx.doi.org/10.1177/109158189901800208.
Texto completoFronczek, Frank R., Richard D. Gandour, Thomas M. Fyles, Philippa J. Hocking, Susan J. McDermid y P. Daniel Wotton. "Polycarboxylate crown ethers from meso-tartaric acid". Canadian Journal of Chemistry 69, n.º 1 (1 de enero de 1991): 12–19. http://dx.doi.org/10.1139/v91-003.
Texto completoSang, Dayong, Jiahui Wang, Yun Zheng, Jianyuan He, Caili Yuan, Qing An y Juan Tian. "Carbodiimides as Acid Scavengers in Aluminum Triiodide Induced Cleavage of Alkyl Aryl Ethers". Synthesis 49, n.º 12 (14 de marzo de 2017): 2721–26. http://dx.doi.org/10.1055/s-0036-1588755.
Texto completoPranowo, Harno Dwi y Chairil Anwar. "INTERACTION BETWEEN Li+ CATION WITH CROWN ETHERS OF Bz15C5, DBz16C5 AND DBz18C6: MOLECULAR MODELING BASE ON MNDO/d SEMIEMPIRICAL METHOD". Indonesian Journal of Chemistry 3, n.º 1 (7 de junio de 2010): 55–66. http://dx.doi.org/10.22146/ijc.21906.
Texto completoSzemenyei, Balázs, Balázs Novotny, Sarolta Zsolnai, Zsombor Miskolczy, László Biczók, Attila Takács, László Kollár, László Drahos, Ildikó Móczár y Péter Huszthy. "Push or Pull for a Better Selectivity? A Study on the Electronic Effects of Substituents of the Pyridine Ring on the Enantiomeric Recognition of Chiral Pyridino-18-Crown-6 Ethers". Symmetry 12, n.º 11 (30 de octubre de 2020): 1795. http://dx.doi.org/10.3390/sym12111795.
Texto completoOllevier, Thierry y Topwe M. Mwene-Mbeja. "Diastereoselective bismuth triflate catalyzed Claisen rearrangement of 2-alkoxycarbonyl-substituted allyl vinyl ethers". Canadian Journal of Chemistry 86, n.º 3 (1 de marzo de 2008): 209–12. http://dx.doi.org/10.1139/v07-149.
Texto completoHosoya, Akihiro, Tadashi Narita y Hiroshi Hamana. "Radical Additions of Heptafluoropropyl Trifluorovinyl Ether". Collection of Czechoslovak Chemical Communications 73, n.º 12 (2008): 1663–70. http://dx.doi.org/10.1135/cccc20081663.
Texto completoSchuster, Judith, Jessica Purswani, Uta Breuer, Clementina Pozo, Hauke Harms, Roland H. Müller y Thore Rohwerder. "Constitutive Expression of the Cytochrome P450 EthABCD Monooxygenase System Enables Degradation of Synthetic Dialkyl Ethers in Aquincola tertiaricarbonis L108". Applied and Environmental Microbiology 79, n.º 7 (25 de enero de 2013): 2321–27. http://dx.doi.org/10.1128/aem.03348-12.
Texto completoTaniguchi, Takashi, Yasuaki Taketomo, Mizuki Moriyama, Noritada Matsuo y Yoo Tanabe. "Synthesis and Stereostructure-Activity Relationship of Novel Pyrethroids Possessing two Asymmetric Centers on a Cyclopropane Ring". Molecules 24, n.º 6 (14 de marzo de 2019): 1023. http://dx.doi.org/10.3390/molecules24061023.
Texto completoAikawa, Haruo, Tetsuro Kaneko, Naoki Asao y Yoshinori Yamamoto. "Gold-catalyzed alkylation of silyl enol ethers with ortho-alkynylbenzoic acid esters". Beilstein Journal of Organic Chemistry 7 (20 de mayo de 2011): 648–52. http://dx.doi.org/10.3762/bjoc.7.76.
Texto completoŠtěpánek, Petr, Ondřej Vích, Lukáš Werner, Ladislav Kniežo, Hana Dvořáková y Pavel Vojtíšek. "Stereoselective Preparation of Precursors of α-C-(1→3)-Disaccharides". Collection of Czechoslovak Chemical Communications 70, n.º 9 (2005): 1411–28. http://dx.doi.org/10.1135/cccc20051411.
Texto completoMasiunas, John B. "Tomato (Lycopersicon esculentum) Tolerance to Diphenyl Ether Herbicides Applied Postemergence". Weed Technology 3, n.º 4 (diciembre de 1989): 602–7. http://dx.doi.org/10.1017/s0890037x00032887.
Texto completoSamoylov, V. O., T. I. Stolonogova, D. N. Ramazanov, E. V. Tyurina, V. A. Lavrent'ev, Yu I. Porukova, E. A. Chernysheva y V. M. Kapustin. "tert-Butyl Ethers of Renewable Diols as Oxygenated Additives for Motor Gasoline. Part I: Glycerol and Propylene Glycol Ethers". Нефтехимия 63, n.º 2 (15 de abril de 2023): 220–30. http://dx.doi.org/10.31857/s0028242123020065.
Texto completoSchaefer, Ted, Kerry J. Cox, Cherrie L. Morier, Christian Beaulieu, Rudy Sebastian y Glenn H. Penner. "Motion about the bond in benzyl OR (R = CH3, CH2CH3, CH(CH3)2, C(CH3)3). Solvent and substituent dependence". Canadian Journal of Chemistry 68, n.º 9 (1 de septiembre de 1990): 1553–58. http://dx.doi.org/10.1139/v90-240.
Texto completoEsseffar, M'hamed, Mohamed El Mouhtadi, José-Luis M. Abboud, José Elguero y Daniel Liotard. "Étude théorique (AM1) de l'affinité protonique des polyéthers cycliques (éthers couronnes) et non cycliques (glymes)". Canadian Journal of Chemistry 69, n.º 12 (1 de diciembre de 1991): 1970–75. http://dx.doi.org/10.1139/v91-283.
Texto completoLi, Yiting, Song Sun, Jiang Cheng y Jin-Tao Yu. "Alkylarylation of N-allylbenzamides and N-allylanilines with simple ethers for the direct construction of ether substituted dihydroisoquinolinones and indolines". Organic & Biomolecular Chemistry 18, n.º 4 (2020): 650–54. http://dx.doi.org/10.1039/c9ob02565k.
Texto completoAnantanarayan, Ashok y Thomas M. Fyles. "Polycarboxylate diaza crown ethers derived from R,R-(+)-tartaric acid: synthesis and complexation of metal ions". Canadian Journal of Chemistry 68, n.º 8 (1 de agosto de 1990): 1338–51. http://dx.doi.org/10.1139/v90-206.
Texto completoMetzger, Pierre y Eliette Casadevall. "Botryococcoid ethers, ether lipids from Botryococcus braunii". Phytochemistry 30, n.º 5 (enero de 1991): 1439–44. http://dx.doi.org/10.1016/0031-9422(91)84181-q.
Texto completoPerrott, A. L., H. J. P. De Lijser y D. R. Arnold. "The importance of conformational effects on the carbon–carbon bond cleavage of β-phenethyl ether radical cations". Canadian Journal of Chemistry 75, n.º 4 (1 de abril de 1997): 384–97. http://dx.doi.org/10.1139/v97-044.
Texto completoSaengarun, Chakrapong, Amorn Petsom y Duangamol Nuntasri Tungasmita. "Etherification of Glycerol with Propylene or 1-Butene for Fuel Additives". Scientific World Journal 2017 (2017): 1–11. http://dx.doi.org/10.1155/2017/4089036.
Texto completoTaguchi, Hiroyasu, Bela Paal y Wilfred L. F. Armarego. "Glyceryl-Ether Monooxygenase [EC 1.14.16.5J Part VIII. Probing the Nature of the Active Site". Pteridines 6, n.º 2 (mayo de 1995): 45–57. http://dx.doi.org/10.1515/pteridines.1995.6.2.45.
Texto completoMao, Ying, Min Cao, Xiaoguang Pan, Jiancheng Huang, Jing Li, Liren Xu y Lei Liu. "Bimolecular oxidative C–H alkynylation of α-substituted isochromans". Organic Chemistry Frontiers 6, n.º 12 (2019): 2028–31. http://dx.doi.org/10.1039/c9qo00352e.
Texto completoHan, Jianhua, Kuanyu Yuan, Cheng Liu, Jinyan Wang y Xigao Jian. "Donor–acceptor copolymers containing the phthalazinone–thiophene structure synthesized by classical nucleophilic aromatic polymerization". RSC Advances 5, n.º 39 (2015): 30445–55. http://dx.doi.org/10.1039/c5ra03771a.
Texto completoMulero, A., I. Cachadiña y A. Becerra. "Recommended Correlations for the Surface Tension of Ethers". Journal of Physical and Chemical Reference Data 52, n.º 1 (1 de marzo de 2023): 013103. http://dx.doi.org/10.1063/5.0139446.
Texto completoJiang, Dandan, Jun Xiao, Yingzhen Zhang, Kunming Liu, Juanhua Li y Jinbiao Liu. "Lewis Acid-Initiated Ring-Opening Reactions of Five- and Six-Membered Cyclic Ethers Based on the Oxonium Ylide Intermediates". Organics 5, n.º 3 (22 de julio de 2024): 219–36. http://dx.doi.org/10.3390/org5030011.
Texto completoJin, Qingwu y Robert M. Coates. "Synthesis of Methoxynor Polyisoprenoid Alcohols by Alkylation of (3-Methoxyallyl)lithium Reagents". Collection of Czechoslovak Chemical Communications 67, n.º 1 (2002): 55–74. http://dx.doi.org/10.1135/cccc20020055.
Texto completoLi, Jianxiao, Dan He, Zidong Lin, Liying Cen, Wanqing Wu y Huanfeng Jiang. "NHC–palladium-catalyzed ionic liquid-accelerated regioselective oxyarylation of alkynes with diaryl ethers". Green Chemistry 24, n.º 5 (2022): 1983–88. http://dx.doi.org/10.1039/d1gc04556c.
Texto completoZaharani, Lia y Nader Ghaffari Khaligh. "Recent Developments in Catalytic Reductive Etherifications". Malaysian Catalysis-An International Journal 2, n.º 1 (21 de octubre de 2022): 21–31. http://dx.doi.org/10.22452/mcij.vol2no1.2.
Texto completoZimnicka, Magdalena M. "Crown ethers as shift reagents in peptide epimer differentiation –conclusions from examination of ac-(H)FRW-NH2 petide sequences". International Journal for Ion Mobility Spectrometry 23, n.º 2 (octubre de 2020): 177–88. http://dx.doi.org/10.1007/s12127-020-00271-2.
Texto completoTian, Juan, Dayong Sang, Xiaodong Tu, Zhoujun He y Ming Yao. "Cleavage of Catechol Monoalkyl Ethers by Aluminum Triiodide–Dimethyl Sulfoxide". Synthesis 51, n.º 03 (26 de septiembre de 2018): 704–12. http://dx.doi.org/10.1055/s-0037-1610996.
Texto completoBaumstark, Alfons L., Franci Kovac y Pedro C. Vasquez. "Oxidation of secondary alcohols and ethers by dimethyldioxirane". Canadian Journal of Chemistry 77, n.º 3 (1 de marzo de 1999): 308–12. http://dx.doi.org/10.1139/v99-011.
Texto completoBrowning, Randall G. y Steven C. Curry. "Effect of Glycol Ethers on Plasma Osmolality". Human & Experimental Toxicology 11, n.º 6 (noviembre de 1992): 488–90. http://dx.doi.org/10.1177/096032719201100608.
Texto completoRagauskas, Arthur J. y J. B. Stothers. "13C magnetic resonance studies. 119. Tricyclo[3.3.0.0] and [3.2.1.0]octanones from substituted norbornenones via cyclopropanation and homoketonization". Canadian Journal of Chemistry 63, n.º 11 (1 de noviembre de 1985): 2961–68. http://dx.doi.org/10.1139/v85-491.
Texto completoOh, Young-Ho, Ju Gyeong Jeong, Dong Wook Kim y Sungyul Lee. "Nucleophilic Reactions Using Alkali Metal Fluorides Activated by Crown Ethers and Derivatives". Catalysts 13, n.º 3 (27 de febrero de 2023): 479. http://dx.doi.org/10.3390/catal13030479.
Texto completoDian, Longyang, Qingyu Xing, Daisy Zhang-Negrerie y Yunfei Du. "Direct functionalization of alkyl ethers to construct hemiaminal ether skeletons (HESs)". Organic & Biomolecular Chemistry 16, n.º 24 (2018): 4384–98. http://dx.doi.org/10.1039/c8ob00793d.
Texto completoVaughn, Steven F. y Gayland F. Spencer. "Synthesis and Herbicidal Activity of Modified Monoterpenes Structurally Similar to Cinmethylin". Weed Science 44, n.º 1 (marzo de 1996): 7–11. http://dx.doi.org/10.1017/s0043174500093474.
Texto completoPLOTNIKOVA, R. N., V. I. KORCHAGIN y L. V. POPOVA. "Evaluation of the possibility of using brominated phthalates from production waste as a plasticizer-flame retardant for cellulose ethers". Plasticheskie massy 1, n.º 5-6 (9 de agosto de 2022): 50–52. http://dx.doi.org/10.35164/0554-2901-2022-5-6-50-52.
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