Добірка наукової літератури з теми "Furfuryl ethers"
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Статті в журналах з теми "Furfuryl ethers"
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 джерелаДисертації з теми "Furfuryl ethers"
Iben, Ayad Anas. "Développement de nanocatalyse en flux continu : scale-up de la valorisation de la biomasse." Electronic Thesis or Diss., Compiègne, 2021. http://www.theses.fr/2021COMP2655.
Повний текст джерелаThe objectives of this PhD work were the development of new Pd NPs (nanocatalysts) by green methods and their application on continuous flow to valorisation of biomass derivatives. We first developed the synthesis of nanocatalysts made up of Pd NPs, which are stabilized with oxygen-based ligands, the family of hydroxyl methylene bisphosphonic acid (HMBP). These molecules have enabled us to keep the solutions of Pd NPs stable in water and under aerobic conditions at 4 oc for a period of time more than 6 months after their preparation without any loss in catalytic activity. These solutions of Pd NPs were able to catalyse up to 6 different organic reactions in an aqueous medium under benign conditions, such as the reduction of 4-nitrophenol. The Pd NPs, show high catalytic efficiency for catalytic reduction of 4-nitrophenol by utilizing sodium borohydride as the reducer in contrast to numerous different mNPs catalysts. The complete kinetics of the reduction procedure has been examined by changing a particular factor each time, as the quantity of Pd NPs, NaBH4 concentration, and initial 4-nitrophenol at several experimental circumstances. The assessment of diffusion control was shown by the counting of second Damköhler number. The theoretical values obtained from the Langmuir-Hinshelwood equation were successfully fitted to the experimental data. The present thesis work evaluated an alternative approach to maximize the accessibility of catalytic sites and prevent Pd leaching by the use of unsupported Pd NPs in a microreactor. This study was done by using different microreactors configurations such as PTFE spiral capillary microreactor (SCM) and their applications on the benchmark reaction model of 4-nitrophenol reduction. Briefly, in terms of furfuryl ethyl ether synthesis, we tested different heterogeneous catalysts in continuous flow reactor. The reductive etherification of furfural was done over various metals supported on activated carbon. Due to the best furfuryl ethyl ether selectively, the commercial Pd/C catalyst that contains NPs of Pd was the chosen one. we used a commercial packed-bed reactor (H-cub) over a commercial Pd/C catalyst that contains NPs of Pd. The PUC catalyst was kept in a cartridge that is placed in the reactor module, through which the solvent with reagents is passed. In all studies, the optimization processes was focused on several key points such as temperature, percentage of TFA acid and Pd/C catalysts. Regardless of the study's promising results and advantages, numerous possibilities can be recommended to proceed with the work commenced in this PhD. Thus, additional research can be done to discover alternative nanocatal Sts, ideall hetero eneous ones when utilizin continuous flow
Частини книг з теми "Furfuryl ethers"
Tsubuki, Masayoshi, Kazunori Takahashi, and Toshio Honda. "Stereospecific Construction of (β-Isopropenyl Alcohol Moiety at the C(2) and (3) of Kallolide A and Pinnatin A Using [2,3] Wittig Rearrangement of Cyclic Furfuryl Ethers." In 19th International Congress on Heterocyclic Chemistry, 383. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50375-0.
Повний текст джерелаТези доповідей конференцій з теми "Furfuryl ethers"
Merino, P., T. Tejero, S. Anoro, and F. Merchan. "1,3-Dipolar Cycloadditions of N-Benzyl Furfuryl Nitrones to Vinyl Ethers and a,b-Unsatureted Esters." In The 3rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01718.
Повний текст джерела