Littérature scientifique sur le sujet « Furfuryl ethers »
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Articles de revues sur le sujet "Furfuryl ethers"
Velea, Sanda, Mihaela Bombos, Gabriel Vasilievici, Rami Doukeh et Dorin Bombos. « Component for Gasoline by Hydroconversion of Furfural Derivates in Presence of Methanol ». Revista de Chimie 68, no 7 (15 août 2017) : 1512–17. http://dx.doi.org/10.37358/rc.17.7.5706.
Texte intégralLópez-Asensio, Raquel, Carmen Jiménez Gómez, Cristina García Sancho, Ramón Moreno-Tost, Juan Cecilia et 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 (14 février 2019) : 828. http://dx.doi.org/10.3390/ijms20040828.
Texte intégralChiyonobu, Kazuhiko, Gen-ichi Konishi, Yohtaro Inoue et Kazuhiko Mizuno. « Intramolecular (4π+4π) Photocycloaddition via Naphthalene-Furan Exciplex ». Journal of Chemical Research 2001, no 4 (avril 2001) : 135–37. http://dx.doi.org/10.3184/030823401103169432.
Texte intégralOparina, L. A., O. V. Vysotskaya, A. V. Stepanov, I. A. Ushakov, K. A. Apartsin, N. K. Gusarova et B. A. Trofimov. « Furfuryl vinyl ethers in [4+2]-cycloaddition reactions ». Russian Journal of Organic Chemistry 53, no 2 (février 2017) : 203–9. http://dx.doi.org/10.1134/s1070428017020105.
Texte intégralTsubuki, Masayoshi, Teruyoshi Kamata, Michiyu Nakatani, Keiko Yamazaki, Tomomi Matsui et Toshio Honda. « Asymmetric [2,3] Wittig rearrangement of crotyl furfuryl ethers ». Tetrahedron : Asymmetry 11, no 23 (décembre 2000) : 4725–36. http://dx.doi.org/10.1016/s0957-4166(00)00467-5.
Texte intégralRusakov, Yu Yu, L. B. Krivdin, L. M. Sinegovskaya, N. V. Istomina, L. A. Oparina, A. V. Stepanov et B. A. Trofimov. « Synthesis and conformational analysis of furfuryl vinyl ethers ». Russian Chemical Bulletin 57, no 10 (octobre 2008) : 2132–38. http://dx.doi.org/10.1007/s11172-008-0289-z.
Texte intégralCao, Quan, Wei Zhang, Shengjun Luo, Rongbo Guo et Dongyan Xu. « Synthesis of Furanic Ethers from Furfuryl Alcohol for Biofuel Production ». Energy & ; Fuels 35, no 15 (12 juillet 2021) : 12725–33. http://dx.doi.org/10.1021/acs.energyfuels.1c01061.
Texte intégralOparina, L. A., O. V. Vysotskaya, A. V. Stepanov, N. K. Gusarova et B. A. Trofimov. « Chemo- and regioselective reaction of vinyl furfuryl ethers with alcohols ». Russian Journal of Organic Chemistry 48, no 9 (septembre 2012) : 1162–67. http://dx.doi.org/10.1134/s1070428012090023.
Texte intégralTsubuki, Masayoshi, Teruyoshi Kamata, Michiyu Nakatani, Keiko Yamazaki, Tomomi Matsui et Toshio Honda. « ChemInform Abstract : Asymmetric [2,3] Wittig Rearrangement of Crotyl Furfuryl Ethers. » ChemInform 32, no 19 (8 mai 2001) : no. http://dx.doi.org/10.1002/chin.200119099.
Texte intégralTsubuki, Masayoshi, Akira Ohinata, Tomoaki Tanaka, Kazunori Takahashi et Toshio Honda. « Studies on Wittig rearrangement of furfuryl ethers in steroidal side chain synthesis ». Tetrahedron 61, no 5 (janvier 2005) : 1095–100. http://dx.doi.org/10.1016/j.tet.2004.11.055.
Texte intégralThèses sur le sujet "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.
Texte intégralThe 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
Chapitres de livres sur le sujet "Furfuryl ethers"
Tsubuki, Masayoshi, Kazunori Takahashi et 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 ». Dans 19th International Congress on Heterocyclic Chemistry, 383. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50375-0.
Texte intégralActes de conférences sur le sujet "Furfuryl ethers"
Merino, P., T. Tejero, S. Anoro et F. Merchan. « 1,3-Dipolar Cycloadditions of N-Benzyl Furfuryl Nitrones to Vinyl Ethers and a,b-Unsatureted Esters ». Dans The 3rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland : MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01718.
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