Статті в журналах з теми "Furans Conversion"
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Rivas, Sandra, María Jesús González-Muñoz, Valentín Santos, and Juan Carlos Parajó. "Production of furans from hemicellulosic saccharides in biphasic reaction systems." Holzforschung 67, no. 8 (December 1, 2013): 923–29. http://dx.doi.org/10.1515/hf-2013-0017.
Повний текст джерелаYuliati, Frita, Peter J. Deuss, Hero J. Heeres, and Francesco Picchioni. "Towards Thermally Reversible Networks Based on Furan-Functionalization of Jatropha Oil." Molecules 25, no. 16 (August 10, 2020): 3641. http://dx.doi.org/10.3390/molecules25163641.
Повний текст джерелаYang, Yanliang, Dongsheng Deng, Dong Sui, Yanfu Xie, Dongmi Li, and Ying Duan. "Facile Preparation of Pd/UiO-66-v for the Conversion of Furfuryl Alcohol to Tetrahydrofurfuryl Alcohol under Mild Conditions in Water." Nanomaterials 9, no. 12 (November 28, 2019): 1698. http://dx.doi.org/10.3390/nano9121698.
Повний текст джерелаMao, Yanli, and François Mathey. "The Conversion of Furans into Phosphinines." Chemistry – A European Journal 17, no. 38 (August 11, 2011): 10745–51. http://dx.doi.org/10.1002/chem.201100834.
Повний текст джерелаKumar, Hemant, and Marco Fraaije. "Conversion of Furans by Baeyer-Villiger Monooxygenases." Catalysts 7, no. 6 (June 7, 2017): 179. http://dx.doi.org/10.3390/catal7060179.
Повний текст джерелаHu, Xun, Roel J. M. Westerhof, Liping Wu, Dehua Dong, and Chun-Zhu Li. "Upgrading biomass-derived furans via acid-catalysis/hydrogenation: the remarkable difference between water and methanol as the solvent." Green Chemistry 17, no. 1 (2015): 219–24. http://dx.doi.org/10.1039/c4gc01826e.
Повний текст джерелаWang, Ting, Xianming Guo, Tao Chen, and Juan Li. "The Pd(0) and Pd(ii) cocatalyzed isomerization of alkynyl epoxides to furans: a mechanistic investigation using DFT calculations." Dalton Transactions 49, no. 27 (2020): 9223–30. http://dx.doi.org/10.1039/d0dt00965b.
Повний текст джерелаGuillard, Jér̂ome, Otto Meth-Cohn, Charles W. Rees, Andrew J. P. White, and David J. Williams. "Direct conversion of macrocyclic furans into macrocyclic isothiazoles." Chemical Communications, no. 3 (January 17, 2002): 232–33. http://dx.doi.org/10.1039/b110287g.
Повний текст джерелаPelter, Andrew, and Martin Rowlands. "The conversion of furans to 2(3H)-butenolides." Tetrahedron Letters 28, no. 11 (January 1987): 1203–6. http://dx.doi.org/10.1016/s0040-4039(00)95326-7.
Повний текст джерелаXu, Lujiang, Yuanye Jiang, Qian Yao, Zheng Han, Ying Zhang, Yao Fu, Qingxiang Guo, and George W. Huber. "Direct production of indoles via thermo-catalytic conversion of bio-derived furans with ammonia over zeolites." Green Chemistry 17, no. 2 (2015): 1281–90. http://dx.doi.org/10.1039/c4gc02250e.
Повний текст джерелаLaaman, Sean M., Otto Meth-Cohn, and Charles W. Rees. "The Ready Conversion of 2,5-Disubstituted Furans into Isothiazoles." Synthesis 1999, no. 05 (May 1999): 757–59. http://dx.doi.org/10.1055/s-1999-3480.
Повний текст джерелаParr, Brendan T., Samantha A. Green, and Huw M. L. Davies. "Rhodium-Catalyzed Conversion of Furans to Highly Functionalized Pyrroles." Journal of the American Chemical Society 135, no. 12 (March 14, 2013): 4716–18. http://dx.doi.org/10.1021/ja401386z.
Повний текст джерелаMatsagar, B. M., M. K. Munshi, A. A. Kelkar, and P. L. Dhepe. "Conversion of concentrated sugar solutions into 5-hydroxymethyl furfural and furfural using Brönsted acidic ionic liquids." Catalysis Science & Technology 5, no. 12 (2015): 5086–90. http://dx.doi.org/10.1039/c5cy00858a.
Повний текст джерелаJaeger, M., and M. Mayer. "The Noell Conversion Process – a gasification process for the pollutant-free disposal of sewage sludge and the recovery of energy and materials." Water Science and Technology 41, no. 8 (April 1, 2000): 37–44. http://dx.doi.org/10.2166/wst.2000.0140.
Повний текст джерелаLang, Man, and Hao Li. "Value-added hydrodeoxygenation conversion of biomass." Biomass Science & Technology 1, no. 1 (June 30, 2023): 1–8. http://dx.doi.org/10.61187/bst.v1i1.10.
Повний текст джерелаHu, Xun, Sri Kadarwati, Yao Song, and Chun-Zhu Li. "Simultaneous hydrogenation and acid-catalyzed conversion of the biomass-derived furans in solvents with distinct polarities." RSC Advances 6, no. 6 (2016): 4647–56. http://dx.doi.org/10.1039/c5ra22414d.
Повний текст джерелаBriel, Detlef. "Synthesis and Conversion of 3-(2-Hydroxythiobenzamido)benzo[b]furans." HETEROCYCLES 65, no. 6 (2005): 1295. http://dx.doi.org/10.3987/com-04-10238.
Повний текст джерелаClive, Derrick L. J., Minaruzzaman та Ligong Ou. "Conversion of Furans into γ-Hydroxybutenolides: Use of Sodium Chlorite". Journal of Organic Chemistry 70, № 8 (квітень 2005): 3318–20. http://dx.doi.org/10.1021/jo0402935.
Повний текст джерелаZhou, Xuanmu, Zehui Zhang, Bing Liu, Quan Zhou, Shuguo Wang, and Kejian Deng. "Catalytic conversion of fructose into furans using FeCl3 as catalyst." Journal of Industrial and Engineering Chemistry 20, no. 2 (March 2014): 644–49. http://dx.doi.org/10.1016/j.jiec.2013.05.028.
Повний текст джерелаGuillard, Jerome, Otto Meth-Cohn, Charles W. Rees, Andrew J. P. White, and David J. Williams. "ChemInform Abstract: Direct Conversion of Macrocyclic Furans into Macrocyclic Isothiazoles." ChemInform 33, no. 20 (May 21, 2010): no. http://dx.doi.org/10.1002/chin.200220096.
Повний текст джерелаXia, Shengpeng, Chenyang Wang, Yu Chen, Shunshun Kang, Kun Zhao, Anqing Zheng, Zengli Zhao, and Haibin Li. "Sustainable Aromatic Production from Catalytic Fast Pyrolysis of 2-Methylfuran over Metal-Modified ZSM-5." Catalysts 12, no. 11 (November 20, 2022): 1483. http://dx.doi.org/10.3390/catal12111483.
Повний текст джерелаLópez, Mar, Carlos Vila, Valentín Santos, and Juan Carlos Parajó. "Manufacture of Platform Chemicals from Pine Wood Polysaccharides in Media Containing Acidic Ionic Liquids." Polymers 12, no. 6 (May 27, 2020): 1215. http://dx.doi.org/10.3390/polym12061215.
Повний текст джерелаMarshall, James A., and Gary S. Bartley. "Observations Regarding the Ag(I)-Catalyzed Conversion of Allenones to Furans." Journal of Organic Chemistry 59, no. 23 (November 1994): 7169–71. http://dx.doi.org/10.1021/jo00102a056.
Повний текст джерелаParr, Brendan T., Samantha A. Green, and Huw M. L. Davies. "ChemInform Abstract: Rhodium-Catalyzed Conversion of Furans to Highly Functionalized Pyrroles." ChemInform 44, no. 37 (August 22, 2013): no. http://dx.doi.org/10.1002/chin.201337095.
Повний текст джерелаLaaman, Sean M., Otto Meth-Cohn, and Charles W. Rees. "ChemInform Abstract: The Ready Conversion of 2,5-Disubstituted Furans into Isothiazoles." ChemInform 30, no. 35 (June 13, 2010): no. http://dx.doi.org/10.1002/chin.199935147.
Повний текст джерелаZhu, Lijuan, Minghui Fan, Yulan Wang, Shengfei Wang, Yuting He, and Quanxin Li. "Selective conversion of furans to p ‐xylene with surface‐modified zeolites." Journal of Chemical Technology & Biotechnology 94, no. 9 (June 12, 2019): 2876–87. http://dx.doi.org/10.1002/jctb.6090.
Повний текст джерелаZhang, Zehui, and Zongbao K. Zhao. "Microwave-assisted conversion of lignocellulosic biomass into furans in ionic liquid." Bioresource Technology 101, no. 3 (February 2010): 1111–14. http://dx.doi.org/10.1016/j.biortech.2009.09.010.
Повний текст джерелаBarešić, Luka, Davor Margetić, and Zoran Glasovac. "Cycloaddition of Thiourea- and Guanidine-Substituted Furans to Dienophiles: A Comparison of the Environmentally-Friendly Methods." Chemistry Proceedings 3, no. 1 (November 14, 2020): 57. http://dx.doi.org/10.3390/ecsoc-24-08380.
Повний текст джерелаEl Arba, Marie, Sara E. Dibrell, Frederick Meece, and Doug E. Frantz. "Ru(II)-Catalyzed Synthesis of Substituted Furans and Their Conversion to Butenolides." Organic Letters 20, no. 18 (September 11, 2018): 5886–88. http://dx.doi.org/10.1021/acs.orglett.8b02554.
Повний текст джерелаSong, Zhi Zhong, Mei Sing Ho, and Henry N. C. Wong. "Regiospecific synthesis of 3,4-disubstituted furans. 7. Synthesis and reactions of 3,4-bis(trimethylsilyl)furan: Diels-Alder cycloaddition, Friedel-Crafts acylation, and regiospecific conversion to 3,4-disubstituted furans." Journal of Organic Chemistry 59, no. 14 (July 1994): 3917–26. http://dx.doi.org/10.1021/jo00093a025.
Повний текст джерелаSong, Zhi Zhong, Zhong Yuan Zhou, Thomas C. W. Mak, and Henry N. C. Wong. "Regiospecific Conversion of 3,4-Bis(trimethylsilyl)furan to 3,4-Disubstituted Furans: A Novel Suzuki-Type Cross-Coupling of Boroxines." Angewandte Chemie International Edition in English 32, no. 3 (March 1993): 432–34. http://dx.doi.org/10.1002/anie.199304321.
Повний текст джерелаTao, Furong, Huanling Song, and Lingjun Chou. "Efficient conversion of cellulose into furans catalyzed by metal ions in ionic liquids." Journal of Molecular Catalysis A: Chemical 357 (May 2012): 11–18. http://dx.doi.org/10.1016/j.molcata.2012.01.010.
Повний текст джерелаLuo, Jia, Yong Xu, Lingjie Zhao, Linlin Dong, Dongmei Tong, Liangfang Zhu, and Changwei Hu. "Two-step hydrothermal conversion of Pubescens to obtain furans and phenol compounds separately." Bioresource Technology 101, no. 22 (November 2010): 8873–80. http://dx.doi.org/10.1016/j.biortech.2010.06.097.
Повний текст джерелаMARSHALL, J. A., and G. S. BARTLEY. "ChemInform Abstract: Observations Regarding the Ag(I)-Catalyzed Conversion of Allenones to Furans." ChemInform 26, no. 23 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199523108.
Повний текст джерелаKarod, Madeline, Zoe A. Pollard, Maisha T. Ahmad, Guolan Dou, Lihui Gao, and Jillian L. Goldfarb. "Impact of Bentonite Clay on In Situ Pyrolysis vs. Hydrothermal Carbonization of Avocado Pit Biomass." Catalysts 12, no. 6 (June 15, 2022): 655. http://dx.doi.org/10.3390/catal12060655.
Повний текст джерелаSONG, Z. Z., M. S. HO, and H. N. C. WONG. "ChemInform Abstract: Regiospecific Synthesis of 3,4-Disubstituted Furans. Part 7. Synthesis and Reactions of 3,4-Bis(trimethylsilyl)furan: Diels-Alder Cycloaddition, Friedel-Crafts Acylation, and Regiospecific Conversion to 3,4-Disubstituted Furans." ChemInform 26, no. 1 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199501136.
Повний текст джерелаWanjala, George W., Arnold N. Onyango, David Abuga, Calvin Onyango, and Moses Makayoto. "Does lysine drive the conversion of fatty acid hydroperoxides to aldehydes and alkyl-furans?" Scientific African 12 (July 2021): e00797. http://dx.doi.org/10.1016/j.sciaf.2021.e00797.
Повний текст джерелаTiecco, Marcello, Lorenzo Testaferri, Marco Tingoli та Francesca Marini. "Selenium Promoted Conversion of α-Substituted β,γ-Unsaturated Ketones into 2,3,5-Trisubstituted Furans". Synlett 1994, № 05 (1994): 373–74. http://dx.doi.org/10.1055/s-1994-22859.
Повний текст джерелаLee, Phil Ho, Jong Soon Kim, Youn Chul Kim, and Sunggak Kim. "A facile preparation of highly functionalized cyclopropanes and their conversion to cyclopentanones and furans." Tetrahedron Letters 34, no. 47 (November 1993): 7583–86. http://dx.doi.org/10.1016/s0040-4039(00)60406-9.
Повний текст джерелаRonaghi, Nima, David M. Fialho, Christopher W. Jones, and Stefan France. "Conversion of Unprotected Aldose Sugars to Polyhydroxyalkyl and C-Glycosyl Furans via Zirconium Catalysis." Journal of Organic Chemistry 85, no. 23 (November 23, 2020): 15337–46. http://dx.doi.org/10.1021/acs.joc.0c02176.
Повний текст джерелаMettler, Matthew S., Samir H. Mushrif, Alex D. Paulsen, Ashay D. Javadekar, Dionisios G. Vlachos, and Paul J. Dauenhauer. "Revealing pyrolysis chemistry for biofuels production: Conversion of cellulose to furans and small oxygenates." Energy Environ. Sci. 5, no. 1 (2012): 5414–24. http://dx.doi.org/10.1039/c1ee02743c.
Повний текст джерелаPatil, Santoshkumar N., and Fei Liu. "Base-Assisted Regio- and Diastereoselective Conversion of Functionalized Furans to Butenolides Using Singlet Oxygen." Organic Letters 9, no. 2 (January 2007): 195–98. http://dx.doi.org/10.1021/ol062551l.
Повний текст джерелаGaladima, Ahmad, and Oki Muraza. "Zeolite catalyst design for the conversion of glucose to furans and other renewable fuels." Fuel 258 (December 2019): 115851. http://dx.doi.org/10.1016/j.fuel.2019.115851.
Повний текст джерелаRomo, Joelle E., Nathan V. Bollar, Coy J. Zimmermann, and Stephanie G. Wettstein. "Conversion of Sugars and Biomass to Furans Using Heterogeneous Catalysts in Biphasic Solvent Systems." ChemCatChem 10, no. 21 (September 13, 2018): 4805–16. http://dx.doi.org/10.1002/cctc.201800926.
Повний текст джерелаChang, Chu-An, Stefan Gürtzgen, Erik P. Johnson та K. Peter C. Vollhardt. "Stoichiometric and Catalytic (η 5-Cyclopentadienyl)cobalt-Mediated Cycloisomerizations of Ene-Yne-Ene Type Allyl Propargyl Ethers". Synthesis 52, № 03 (28 жовтня 2019): 399–416. http://dx.doi.org/10.1055/s-0039-1690727.
Повний текст джерелаVan Nguyen, Chi, Jing Rou Boo, Chia-Hung Liu, Tansir Ahamad, Saad M. Alshehri, Babasaheb M. Matsagar, and Kevin C. W. Wu. "Oxidation of biomass-derived furans to maleic acid over nitrogen-doped carbon catalysts under acid-free conditions." Catalysis Science & Technology 10, no. 5 (2020): 1498–506. http://dx.doi.org/10.1039/c9cy02364j.
Повний текст джерелаKannan, P., G. Lakshmanan, A. Al Shoaibi, and C. Srinivasakannan. "Equilibrium model analysis of waste plastics gasification using CO2 and steam." Waste Management & Research: The Journal for a Sustainable Circular Economy 35, no. 12 (November 3, 2017): 1247–53. http://dx.doi.org/10.1177/0734242x17736946.
Повний текст джерелаPatil, Santoshkumar N., та Fei Liu. "Fluoride-Assisted Regioselective Conversion of Functionalized Furans to α-Substituted γ-Hydroxybutenolides Using Singlet Oxygen". Journal of Organic Chemistry 72, № 16 (серпень 2007): 6305–8. http://dx.doi.org/10.1021/jo070666c.
Повний текст джерелаNikbin, Nima, Stavros Caratzoulas, and Dionisios G. Vlachos. "On the oligomerization mechanism of Brønsted acid-catalyzed conversion of furans to diesel-range fuels." Applied Catalysis A: General 485 (September 2014): 118–22. http://dx.doi.org/10.1016/j.apcata.2014.07.035.
Повний текст джерелаKopytko, Ya F. "Quantitative Determination of Total Carbohydrates (Recalculated for Fructose After Conversion to Furans) in Burdock Juice." Pharmaceutical Chemistry Journal 51, no. 4 (July 2017): 285–87. http://dx.doi.org/10.1007/s11094-017-1599-y.
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