Статті в журналах з теми "Furfuryl ethers"
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Velea, Sanda, Mihaela Bombos, Gabriel Vasilievici, Rami Doukeh, and Dorin Bombos. "Component for Gasoline by Hydroconversion of Furfural Derivates in Presence of Methanol." Revista de Chimie 68, no. 7 (August 15, 2017): 1512–17. http://dx.doi.org/10.37358/rc.17.7.5706.
Повний текст джерелаLópez-Asensio, Raquel, Carmen Jiménez Gómez, Cristina García Sancho, Ramón Moreno-Tost, Juan Cecilia, and Pedro Maireles-Torres. "Influence of Structure-modifying Agents in the Synthesis of Zr-doped SBA-15 Silica and Their Use as Catalysts in the Furfural Hydrogenation to Obtain High Value-added Products through the Meerwein-Ponndorf-Verley Reduction." International Journal of Molecular Sciences 20, no. 4 (February 14, 2019): 828. http://dx.doi.org/10.3390/ijms20040828.
Повний текст джерелаChiyonobu, Kazuhiko, Gen-ichi Konishi, Yohtaro Inoue та Kazuhiko Mizuno. "Intramolecular (4π+4π) Photocycloaddition via Naphthalene-Furan Exciplex". Journal of Chemical Research 2001, № 4 (квітень 2001): 135–37. http://dx.doi.org/10.3184/030823401103169432.
Повний текст джерелаOparina, L. A., O. V. Vysotskaya, A. V. Stepanov, I. A. Ushakov, K. A. Apartsin, N. K. Gusarova, and B. A. Trofimov. "Furfuryl vinyl ethers in [4+2]-cycloaddition reactions." Russian Journal of Organic Chemistry 53, no. 2 (February 2017): 203–9. http://dx.doi.org/10.1134/s1070428017020105.
Повний текст джерелаTsubuki, Masayoshi, Teruyoshi Kamata, Michiyu Nakatani, Keiko Yamazaki, Tomomi Matsui, and Toshio Honda. "Asymmetric [2,3] Wittig rearrangement of crotyl furfuryl ethers." Tetrahedron: Asymmetry 11, no. 23 (December 2000): 4725–36. http://dx.doi.org/10.1016/s0957-4166(00)00467-5.
Повний текст джерелаRusakov, Yu Yu, L. B. Krivdin, L. M. Sinegovskaya, N. V. Istomina, L. A. Oparina, A. V. Stepanov, and B. A. Trofimov. "Synthesis and conformational analysis of furfuryl vinyl ethers." Russian Chemical Bulletin 57, no. 10 (October 2008): 2132–38. http://dx.doi.org/10.1007/s11172-008-0289-z.
Повний текст джерелаCao, Quan, Wei Zhang, Shengjun Luo, Rongbo Guo, and Dongyan Xu. "Synthesis of Furanic Ethers from Furfuryl Alcohol for Biofuel Production." Energy & Fuels 35, no. 15 (July 12, 2021): 12725–33. http://dx.doi.org/10.1021/acs.energyfuels.1c01061.
Повний текст джерелаOparina, L. A., O. V. Vysotskaya, A. V. Stepanov, N. K. Gusarova, and B. A. Trofimov. "Chemo- and regioselective reaction of vinyl furfuryl ethers with alcohols." Russian Journal of Organic Chemistry 48, no. 9 (September 2012): 1162–67. http://dx.doi.org/10.1134/s1070428012090023.
Повний текст джерелаTsubuki, Masayoshi, Teruyoshi Kamata, Michiyu Nakatani, Keiko Yamazaki, Tomomi Matsui, and Toshio Honda. "ChemInform Abstract: Asymmetric [2,3] Wittig Rearrangement of Crotyl Furfuryl Ethers." ChemInform 32, no. 19 (May 8, 2001): no. http://dx.doi.org/10.1002/chin.200119099.
Повний текст джерелаTsubuki, Masayoshi, Akira Ohinata, Tomoaki Tanaka, Kazunori Takahashi, and Toshio Honda. "Studies on Wittig rearrangement of furfuryl ethers in steroidal side chain synthesis." Tetrahedron 61, no. 5 (January 2005): 1095–100. http://dx.doi.org/10.1016/j.tet.2004.11.055.
Повний текст джерелаOparina, L. A., O. V. Vysotskaya, A. V. Stepanov, N. K. Gusarova, and B. A. Trofimov. "ChemInform Abstract: Chemo- and Regioselective Reaction of Vinyl Furfuryl Ethers with Alcohols." ChemInform 44, no. 10 (March 5, 2013): no. http://dx.doi.org/10.1002/chin.201310113.
Повний текст джерелаTsubuki, Masayoshi, Teruyoshi Kamata, Hiroyuki Okita, Mayumi Arai, Atsushi Shigihara, and Toshio Honda. "Wittig rearrangement of allyl and propargyl furfuryl ethers leading to 2-furylmethanol derivatives." Chemical Communications, no. 22 (1999): 2263–64. http://dx.doi.org/10.1039/a907312d.
Повний текст джерелаAnisimov, A. V., L. V. Mozhaeva, N. B. Kazennova, S. V. Kuznetsova, and E. A. Viktorova. "Wittig rearrangement of allyl furfuryl and allyl thienyl ethers and sulfides and their benzo-derivatives." Chemistry of Heterocyclic Compounds 23, no. 7 (July 1987): 724–29. http://dx.doi.org/10.1007/bf00475634.
Повний текст джерелаTsubuki, Masayoshi, Teruyoshi Kamata, Hiroyuki Okita, Mayumi Arai, Atsushi Shigihara, and Toshio Honda. "ChemInform Abstract: Wittig Rearrangement of Allyl and Propargyl Furfuryl Ethers Leading to 2-Furylmethanol Derivatives." ChemInform 31, no. 23 (June 8, 2010): no. http://dx.doi.org/10.1002/chin.200023110.
Повний текст джерелаZhu, Xuhai, Bardo Bruijnaers, Tainise V. Lourençon, and Mikhail Balakshin. "Structural Analysis of Lignin-Based Furan Resin." Materials 15, no. 1 (January 4, 2022): 350. http://dx.doi.org/10.3390/ma15010350.
Повний текст джерелаWang, Yun, Qianqian Cui, Yejun Guan, and Peng Wu. "Facile synthesis of furfuryl ethyl ether in high yield via the reductive etherification of furfural in ethanol over Pd/C under mild conditions." Green Chemistry 20, no. 9 (2018): 2110–17. http://dx.doi.org/10.1039/c7gc03887a.
Повний текст джерелаTarabanko, Valery E., Irina L. Simakova, Marina A. Smirnova, and Konstantin L. Kaygorodov. "Catalytic Hydrogenation of Furfural Diethyl Acetal to Ethyl Furfuryl Ether." Journal of Siberian Federal University. Chemistry 14, no. 3 (September 2021): 281–89. http://dx.doi.org/10.17516/1998-2836-0237.
Повний текст джерелаWu, Hsien-Jen, Fu-Hsing Ying, and Wei-Dar Shao. "Study on the reaction mechanism of the base-catalyzed intramolecular Diels-Alder reaction of furfuryl propargyl ethers." Journal of Organic Chemistry 60, no. 19 (September 1995): 6168–72. http://dx.doi.org/10.1021/jo00124a033.
Повний текст джерелаSpillman, Philip J., Alan P. Pollnitz, Dimitra Liacopoulos, Kevin H. Pardon, and Mark A. Sefton. "Formation and Degradation of Furfuryl Alcohol, 5-Methylfurfuryl Alcohol, Vanillyl Alcohol, and Their Ethyl Ethers in Barrel-Aged Wines." Journal of Agricultural and Food Chemistry 46, no. 2 (February 1998): 657–63. http://dx.doi.org/10.1021/jf970559r.
Повний текст джерелаWU, H. J., F. H. YING, and W. D. SHAO. "ChemInform Abstract: Study on the Reaction Mechanism of the Base-Catalyzed Intramolecular Diels-Alder Reaction of Furfuryl Propargyl Ethers." ChemInform 27, no. 6 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.199606081.
Повний текст джерелаGuella, Graziano, Ines Mancini, Aysel Öztunç, and Francesco Pietra. "Conformational Bias in Macrocyclic Ethers and Observation of High Solvolytic Reactivity at a Masked Furfuryl (=2-Furylmethyl) C-Atom." Helvetica Chimica Acta 83, no. 2 (February 16, 2000): 336–48. http://dx.doi.org/10.1002/(sici)1522-2675(20000216)83:2<336::aid-hlca336>3.0.co;2-r.
Повний текст джерелаAldureid, Abdulaziz, Francisco Medina, Gregory S. Patience, and Daniel Montané. "Ni-Cu/Al2O3 from Layered Double Hydroxides Hydrogenates Furfural to Alcohols." Catalysts 12, no. 4 (March 31, 2022): 390. http://dx.doi.org/10.3390/catal12040390.
Повний текст джерелаIglesias, Jose, Juan Melero, Gabriel Morales, Jovita Moreno, Yolanda Segura, Marta Paniagua, Alberto Cambra, and Blanca Hernández. "Zr-SBA-15 Lewis Acid Catalyst: Activity in Meerwein Ponndorf Verley Reduction." Catalysts 5, no. 4 (November 12, 2015): 1911–27. http://dx.doi.org/10.3390/catal5041911.
Повний текст джерелаSaotta, Anna, Alessandro Allegri, Francesca Liuzzi, Giuseppe Fornasari, Nikolaos Dimitratos, and Stefania Albonetti. "Ti/Zr/O Mixed Oxides for the Catalytic Transfer Hydrogenation of Furfural to GVL in a Liquid-Phase Continuous-Flow Reactor." ChemEngineering 7, no. 2 (March 14, 2023): 23. http://dx.doi.org/10.3390/chemengineering7020023.
Повний текст джерелаTsubuki, Masayoshi, Kazunori Takahashi та Toshio Honda. "Stereoselective Construction of a β-Isopropenyl Alcohol Moiety at the C(2) and (3) of Kallolide A and Pinnatin A Using a [2,3] Wittig Rearrangement of Cyclic Furfuryl Ethers". Journal of Organic Chemistry 68, № 26 (грудень 2003): 10183–86. http://dx.doi.org/10.1021/jo035244r.
Повний текст джерелаAldureid, Abdulaziz, Daniel Montané, Jordi Llorca, and Francesc Medina. "Ni-Mg/Al Mixed Oxides Prepared from Double Layered Hydroxides as Catalysts for the Conversion of Furfural to Tetrahydrofurfuryl Alcohol." Chemistry 5, no. 1 (March 9, 2023): 571–88. http://dx.doi.org/10.3390/chemistry5010041.
Повний текст джерелаZaccheria, Federica, Nicola Scotti, and Nicoletta Ravasio. "Solid Acids for the Reaction of Bioderived Alcohols into Ethers for Fuel Applications." Catalysts 9, no. 2 (February 12, 2019): 172. http://dx.doi.org/10.3390/catal9020172.
Повний текст джерелаRoos, Kévin, Elena Dolci, Stéphane Carlotti, and Sylvain Caillol. "Activated anionic ring-opening polymerization for the synthesis of reversibly cross-linkable poly(propylene oxide) based on furan/maleimide chemistry." Polymer Chemistry 7, no. 8 (2016): 1612–22. http://dx.doi.org/10.1039/c5py01778e.
Повний текст джерелаZaccheria, Federica, Filippo Bossola, Nicola Scotti, Claudio Evangelisti, Vladimiro Dal Santo, and Nicoletta Ravasio. "On demand production of ethers or alcohols from furfural and HMF by selecting the composition of a Zr/Si catalyst." Catalysis Science & Technology 10, no. 22 (2020): 7502–11. http://dx.doi.org/10.1039/d0cy01427c.
Повний текст джерелаZiemczonek, Piotr, Monika Gosecka, Mateusz Gosecki, Monika Marcinkowska, Anna Janaszewska, and Barbara Klajnert-Maculewicz. "Star-Shaped Poly(furfuryl glycidyl ether)-Block-Poly(glyceryl glycerol ether) as an Efficient Agent for the Enhancement of Nifuratel Solubility and for the Formation of Injectable and Self-Healable Hydrogel Platforms for the Gynaecological Therapies." International Journal of Molecular Sciences 22, no. 16 (August 4, 2021): 8386. http://dx.doi.org/10.3390/ijms22168386.
Повний текст джерелаAdatia, Karishma K., Alexander Holm, Alexander Southan, Curtis W. Frank, and Günter E. M. Tovar. "Structure–property relations of amphiphilic poly(furfuryl glycidyl ether)-block-poly(ethylene glycol) macromonomers at the air–water interface." Polymer Chemistry 11, no. 35 (2020): 5659–68. http://dx.doi.org/10.1039/d0py00697a.
Повний текст джерелаMikova, Nadezhda Mikhailovna, Elena Valentinovna Mazurova, Ivan Petrovich Ivanov, and Boris Nikolayevich Kuznetsov. "SYNTHESIS, STRUCTURE AND PROPERTIES OF ORGANIC GELS BASED ON LARCH BARK TANNINS AND HY-DROLYSIS LIGNIN." chemistry of plant raw material, no. 2 (June 10, 2021): 109–22. http://dx.doi.org/10.14258/jcprm.2021029635.
Повний текст джерелаHOU, Jiqiang, Lijun QIAO, Jun WEI, Yuxi HU, Xianhong WANG, Xiaojiang ZHAO, and Fosong WANG. "COPOLYMERIZATION OF FURFURYL GLYCIDYL ETHER AND CARBON DIOXIDE." Acta Polymerica Sinica 009, no. 10 (November 6, 2009): 1007–11. http://dx.doi.org/10.3724/sp.j.1105.2009.01007.
Повний текст джерелаMendonça, C. R., N. M. Barbosa Neto, P. S. Batista, M. F. de Souza, and S. C. Zilio. "Dynamic optical nonlinearities in di-furfuryl ether solution." Chemical Physics Letters 361, no. 5-6 (August 2002): 383–88. http://dx.doi.org/10.1016/s0009-2614(02)00998-3.
Повний текст джерелаAntunes, Margarida M., Andreia F. Silva, Carolina D. Bernardino, Auguste Fernandes, Filipa Ribeiro, and Anabela A. Valente. "Catalytic Transfer Hydrogenation and Acid Reactions of Furfural and 5-(Hydroxymethyl)furfural over Hf-TUD-1 Type Catalysts." Molecules 26, no. 23 (November 27, 2021): 7203. http://dx.doi.org/10.3390/molecules26237203.
Повний текст джерелаAdatia, Karishma K., Silke Keller, Tobias Götz, Günter E. M. Tovar, and Alexander Southan. "Hydrogels with multiple clickable anchor points: synthesis and characterization of poly(furfuryl glycidyl ether)-block-poly(ethylene glycol) macromonomers." Polymer Chemistry 10, no. 32 (2019): 4485–94. http://dx.doi.org/10.1039/c9py00755e.
Повний текст джерелаChen, Han, Sisi Zhang, Yuting Zhuang, Juan Zhao, Qiong Xu та Dulin Yin. "Zirconia and Phosphotungstic Acid Supported on TS-1 as An Active Catalyst for One-Pot Selective Conversion of Furfuryl Alcohol to γ-Valerolactone". Science of Advanced Materials 13, № 6 (1 червня 2021): 1078–87. http://dx.doi.org/10.1166/sam.2021.3973.
Повний текст джерелаSofiya, K., K. Anbalagan, A. Richa Elson, I. Fazal Fathima, and M. Vignesh Kumar. "Effect of solvents on the composition of Rosa x damascena concrete oil in multistage solvent extraction." Journal of Applied Horticulture 24, no. 01 (August 17, 2022): 94–97. http://dx.doi.org/10.37855/jah.2022.v24i01.18.
Повний текст джерелаHU, Yuxi, Lijun QIAO, Yusheng QIN, Xianhong WANG, Xiaojiang ZHAO, and Fosong WANG. "DIELS-ALDER REACTION OF FURFURYL GLYCIDYL ETHER/CARBON DIOXIDE COPOLYMER." Acta Polymerica Sinica 011, no. 11 (November 21, 2011): 1336–40. http://dx.doi.org/10.3724/sp.j.1105.2011.11059.
Повний текст джерелаPetrova, T. V., I. V. Tretyakov, and V. I. Solodilov. "Technological Parameters of Epoxypolysulphone Binders Modified with Furfuryl Glycidyl Ether." Russian Journal of Physical Chemistry B 17, no. 1 (February 2023): 177–81. http://dx.doi.org/10.1134/s1990793123010086.
Повний текст джерелаTarabanko, V. E., M. A. Smirnova та E. G. Zhizhina. "Processes for the synthesis of γ-acetopropyl alcohol". Kataliz v promyshlennosti 22, № 2 (24 березня 2022): 5–17. http://dx.doi.org/10.18412/1816-0387-2022-2-5-17.
Повний текст джерелаValadares, Deborah S., Maria Clara H. Clemente, Elon F. de Freitas, Gesley Alex V. Martins, José A. Dias, and Sílvia C. L. Dias. "Niobium on BEA Dealuminated Zeolite for High Selectivity Dehydration Reactions of Ethanol and Xylose into Diethyl Ether and Furfural." Nanomaterials 10, no. 7 (June 29, 2020): 1269. http://dx.doi.org/10.3390/nano10071269.
Повний текст джерелаMulik, Nagesh L., Prashant S. Niphadkar, and Vijay V. Bokade. "Synthesis of ethyl furfuryl ether (potential biofuel) by etherification of furfuryl alcohol with ethanol over heterogenized reusable H1Cs2PW12O40 catalyst." Research on Chemical Intermediates 46, no. 4 (February 3, 2020): 2309–25. http://dx.doi.org/10.1007/s11164-020-04093-z.
Повний текст джерелаMendonça, C. R., P. S. Batista, M. F. de Souza, and S. C. Zilio. "Chemical dynamics and reverse saturable absorption in di-furfuryl ether solutions." Chemical Physics Letters 343, no. 5-6 (August 2001): 499–506. http://dx.doi.org/10.1016/s0009-2614(01)00760-6.
Повний текст джерелаCao, Quan, Jing Guan, Gongming Peng, Tonggang Hou, Jianwei Zhou, and Xindong Mu. "Solid acid-catalyzed conversion of furfuryl alcohol to alkyl tetrahydrofurfuryl ether." Catalysis Communications 58 (January 2015): 76–79. http://dx.doi.org/10.1016/j.catcom.2014.08.030.
Повний текст джерелаBornosuz, Natalia V., Roman F. Korotkov, Vyacheslav V. Shutov, Igor S. Sirotin, and Irina Yu Gorbunova. "Benzoxazine Copolymers with Mono- and Difunctional Epoxy Active Diluents with Enhanced Tackiness and Reduced Viscosity." Journal of Composites Science 5, no. 9 (September 18, 2021): 250. http://dx.doi.org/10.3390/jcs5090250.
Повний текст джерелаNakagawa, Yasuhiro, Kotaro Ushidome, Keita Masuda, Kazunori Igarashi, Yu Matsumoto, Tatsuya Yamasoba, Yasutaka Anraku, Madoka Takai, and Horacio Cabral. "Multi-Armed Star-Shaped Block Copolymers of Poly(ethylene glycol)-Poly(furfuryl glycidol) as Long Circulating Nanocarriers." Polymers 15, no. 12 (June 9, 2023): 2626. http://dx.doi.org/10.3390/polym15122626.
Повний текст джерелаChaffey, Dawn R., Thomas E. Davies, Stuart H. Taylor, and Andrew E. Graham. "Etherification Reactions of Furfuryl Alcohol in the Presence of Orthoesters and Ketals: Application to the Synthesis of Furfuryl Ether Biofuels." ACS Sustainable Chemistry & Engineering 6, no. 4 (March 8, 2018): 4996–5002. http://dx.doi.org/10.1021/acssuschemeng.7b04636.
Повний текст джерелаKawabata, Tomoaki, Yoshie Tanaka, Asako Horinishi, Megumi Mori, Asao Hosoda, Nami Yamamoto, and Takahiko Mitani. "Subcritical Methanol Extraction of the Stone of Japanese Apricot Prunus mume Sieb. et Zucc." Biomolecules 10, no. 7 (July 15, 2020): 1047. http://dx.doi.org/10.3390/biom10071047.
Повний текст джерелаZhang, Chi, and Xing Ping Liu. "Analysis of Chemical Constituents of Volatile Oil of Se-Enriched Selenium Codonopsis tangshen Oliv. GC-MS." Advanced Materials Research 554-556 (July 2012): 1572–76. http://dx.doi.org/10.4028/www.scientific.net/amr.554-556.1572.
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