Статті в журналах з теми "5-chloromethyl furfural"
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Ознайомтеся з топ-41 статей у журналах для дослідження на тему "5-chloromethyl furfural".
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Bizet, Boris, Christian H. Hornung, Thomas M. Kohl, and John Tsanaktsidis. "Synthesis of Imines and Amines from Furfurals Using Continuous Flow Processing." Australian Journal of Chemistry 70, no. 10 (2017): 1069. http://dx.doi.org/10.1071/ch17036.
Повний текст джерелаKohl, T. M., B. Bizet, P. Kevan, C. Sellwood, J. Tsanaktsidis, and C. H. Hornung. "Efficient synthesis of 5-(chloromethyl)furfural (CMF) from high fructose corn syrup (HFCS) using continuous flow processing." Reaction Chemistry & Engineering 2, no. 4 (2017): 541–49. http://dx.doi.org/10.1039/c7re00039a.
Повний текст джерелаZuo, Miao, Zheng Li, Yetao Jiang, Xing Tang, Xianhai Zeng, Yong Sun, and Lu Lin. "Correction: Green catalytic conversion of bio-based sugars to 5-chloromethyl furfural in deep eutectic solvent, catalyzed by metal chlorides." RSC Advances 6, no. 40 (2016): 33492. http://dx.doi.org/10.1039/c6ra90032a.
Повний текст джерелаMascal, Mark, and Saikat Dutta. "Synthesis of ranitidine (Zantac) from cellulose-derived 5-(chloromethyl)furfural." Green Chemistry 13, no. 11 (2011): 3101. http://dx.doi.org/10.1039/c1gc15537g.
Повний текст джерелаDutta, Saikat, and Mark Mascal. "Novel Pathways to 2,5-Dimethylfuran via Biomass-Derived 5-(Chloromethyl)furfural." ChemSusChem 7, no. 11 (September 5, 2014): 3028–30. http://dx.doi.org/10.1002/cssc.201402702.
Повний текст джерелаMascal, Mark, and Edward B Nikitin. "Dramatic Advancements in the Saccharide to 5-(Chloromethyl)furfural Conversion Reaction." ChemSusChem 2, no. 9 (September 21, 2009): 859–61. http://dx.doi.org/10.1002/cssc.200900136.
Повний текст джерелаBhat, Navya Subray, Nivedha Vinod, Sharath Bandibairanahalli Onkarappa, and Saikat Dutta. "Hydrochloric acid-catalyzed coproduction of furfural and 5-(chloromethyl)furfural assisted by a phase transfer catalyst." Carbohydrate Research 496 (October 2020): 108105. http://dx.doi.org/10.1016/j.carres.2020.108105.
Повний текст джерелаDutta, Saikat, Linglin Wu, and Mark Mascal. "Production of 5-(chloromethyl)furan-2-carbonyl chloride and furan-2,5-dicarbonyl chloride from biomass-derived 5-(chloromethyl)furfural (CMF)." Green Chemistry 17, no. 7 (2015): 3737–39. http://dx.doi.org/10.1039/c5gc00936g.
Повний текст джерелаMascal, Mark. "5-(Chloromethyl)furfural (CMF): A Platform for Transforming Cellulose into Commercial Products." ACS Sustainable Chemistry & Engineering 7, no. 6 (March 5, 2019): 5588–601. http://dx.doi.org/10.1021/acssuschemeng.8b06553.
Повний текст джерелаSalim, Kunnummal Mangott Muhammed, Aranhikkal Shamsiya, and Bahulayan Damodaran. "Green Synthesis of Fluorescent Peptidomimetic Triazoles from Biomass-Derived 5-(Chloromethyl)furfural." ChemistrySelect 3, no. 39 (October 24, 2018): 11141–46. http://dx.doi.org/10.1002/slct.201802310.
Повний текст джерелаBreeden, S. W., J. H. Clark, T. J. Farmer, D. J. Macquarrie, J. S. Meimoun, Y. Nonne, and J. E. S. J. Reid. "Microwave heating for rapid conversion of sugars and polysaccharides to 5-chloromethyl furfural." Green Chem. 15, no. 1 (2013): 72–75. http://dx.doi.org/10.1039/c2gc36290b.
Повний текст джерелаChang, Fei, Wan-Hsuan Hsu, and Mark Mascal. "Synthesis of anti-inflammatory furan fatty acids from biomass-derived 5-(chloromethyl)furfural." Sustainable Chemistry and Pharmacy 1 (June 2015): 14–18. http://dx.doi.org/10.1016/j.scp.2015.09.002.
Повний текст джерелаBrasholz, Malte, Karin von Känel, Christian H. Hornung, Simon Saubern, and John Tsanaktsidis. "Highly efficient dehydration of carbohydrates to 5-(chloromethyl)furfural (CMF), 5-(hydroxymethyl)furfural (HMF) and levulinic acid by biphasic continuous flow processing." Green Chemistry 13, no. 5 (2011): 1114. http://dx.doi.org/10.1039/c1gc15107j.
Повний текст джерелаAntonyraj, Churchil A., Amal J. Chennattussery, and Ajit Haridas. "5‐(Chloromethyl)furfural production from glucose: A pioneer kinetic model development exploring the mechanism." International Journal of Chemical Kinetics 53, no. 7 (March 16, 2021): 825–33. http://dx.doi.org/10.1002/kin.21485.
Повний текст джерелаMiao, Haoqian, Huitao Ling, Nikolay Shevchenko, and Mark Mascal. "Generation of Organozinc Nucleophiles Based on the Biomass-Derived Platform Molecule 5-(Chloromethyl)furfural." Organometallics 40, no. 23 (November 15, 2021): 3952–57. http://dx.doi.org/10.1021/acs.organomet.1c00528.
Повний текст джерелаMascal, Mark, та Saikat Dutta. "Synthesis of the natural herbicide δ-aminolevulinic acid from cellulose-derived 5-(chloromethyl)furfural". Green Chem. 13, № 1 (2011): 40–41. http://dx.doi.org/10.1039/c0gc00548g.
Повний текст джерелаChang, Fei, Saikat Dutta, James J. Becnel, Alden S. Estep, and Mark Mascal. "Synthesis of the Insecticide Prothrin and Its Analogues from Biomass-Derived 5-(Chloromethyl)furfural." Journal of Agricultural and Food Chemistry 62, no. 2 (January 3, 2014): 476–80. http://dx.doi.org/10.1021/jf4045843.
Повний текст джерелаDai, Lei, Ye Qiu, Yuan-Yuan Xu, and Song Ye. "Biomass Transformation of Cellulose via N-Heterocyclic Carbene-Catalyzed Umpolung of 5-(Chloromethyl)furfural." Cell Reports Physical Science 1, no. 6 (June 2020): 100071. http://dx.doi.org/10.1016/j.xcrp.2020.100071.
Повний текст джерелаZhang, Ximing, Necla Mine Eren, Thomas Kreke, Nathan S. Mosier, Abigail S. Engelberth, and Gozdem Kilaz. "Concentrated HCl Catalyzed 5-(Chloromethyl)furfural Production from Corn Stover of Varying Particle Sizes." BioEnergy Research 10, no. 4 (July 25, 2017): 1018–24. http://dx.doi.org/10.1007/s12155-017-9860-5.
Повний текст джерелаHoward, Joshua, Darryn W. Rackemann, Zhanying Zhang, Lalehvash Moghaddam, John P. Bartley, and William O. S. Doherty. "Effect of pretreatment on the formation of 5-chloromethyl furfural derived from sugarcane bagasse." RSC Advances 6, no. 7 (2016): 5240–48. http://dx.doi.org/10.1039/c5ra20203e.
Повний текст джерелаMascal, Mark, and Saikat Dutta. "ChemInform Abstract: Synthesis of Ranitidine (Zantac) (VIII) from Cellulose-Derived 5-(Chloromethyl)furfural (I)." ChemInform 43, no. 14 (March 8, 2012): no. http://dx.doi.org/10.1002/chin.201214096.
Повний текст джерелаBreeden, S. W., J. H. Clark, T. J. Farmer, D. J. Macquarrie, J. S. Meimoun, Y. Nonne, and J. E. S. J. Reid. "ChemInform Abstract: Microwave Heating for Rapid Conversion of Sugars and Polysaccharides to 5-Chloromethyl Furfural." ChemInform 44, no. 19 (April 18, 2013): no. http://dx.doi.org/10.1002/chin.201319098.
Повний текст джерелаMascal, Mark, and Edward B. Nikitin. "High-yield conversion of plant biomass into the key value-added feedstocks 5-(hydroxymethyl)furfural, levulinic acid, and levulinic esters via5-(chloromethyl)furfural." Green Chem. 12, no. 3 (2010): 370–73. http://dx.doi.org/10.1039/b918922j.
Повний текст джерелаChen, Binglin, Yunchao Feng, Renjie Huang, Shibo Yang, Zheng Li, Jonathan Sperry, Shuliang Yang, et al. "Efficient synthesis of the liquid fuel 2,5-dimethylfuran from biomass derived 5-(chloromethyl)furfural at room temperature." Applied Catalysis B: Environmental 318 (December 2022): 121842. http://dx.doi.org/10.1016/j.apcatb.2022.121842.
Повний текст джерелаZuo, Miao, Zheng Li, Yetao Jiang, Xing Tang, Xianhai Zeng, Yong Sun, and Lu Lin. "Green catalytic conversion of bio-based sugars to 5-chloromethyl furfural in deep eutectic solvent, catalyzed by metal chlorides." RSC Advances 6, no. 32 (2016): 27004–7. http://dx.doi.org/10.1039/c6ra00267f.
Повний текст джерелаLane, David R., Mark Mascal, and Pieter Stroeve. "Experimental studies towards optimization of the production of 5-(chloromethyl)furfural (CMF) from glucose in a two-phase reactor." Renewable Energy 85 (January 2016): 994–1001. http://dx.doi.org/10.1016/j.renene.2015.07.032.
Повний текст джерелаMascal, Mark. "5-(Chloromethyl)furfural is the New HMF: Functionally Equivalent But More Practical in Terms of its Production From Biomass." ChemSusChem 8, no. 20 (September 16, 2015): 3391–95. http://dx.doi.org/10.1002/cssc.201500940.
Повний текст джерелаBudarin, Vitaliy L., James H. Clark, Jonatan Henschen, Thomas J. Farmer, Duncan J. Macquarrie, Mark Mascal, Gundibasappa K. Nagaraja, and Tabitha H. M. Petchey. "Processed Lignin as a Byproduct of the Generation of 5-(Chloromethyl)furfural from Biomass: A Promising New Mesoporous Material." ChemSusChem 8, no. 24 (November 25, 2015): 4172–79. http://dx.doi.org/10.1002/cssc.201501319.
Повний текст джерелаOnkarappa, Sharath Bandibairanahalli, and Saikat Dutta. "Phase Transfer Catalyst Assisted One‐Pot Synthesis of 5‐(Chloromethyl)furfural from Biomass‐Derived Carbohydrates in a Biphasic Batch Reactor." ChemistrySelect 4, no. 25 (July 2019): 7502–6. http://dx.doi.org/10.1002/slct.201901347.
Повний текст джерелаArnaud, Sacha Pérocheau, Linglin Wu, Maria-Angelica Wong Chang, James W. Comerford, Thomas J. Farmer, Maximilian Schmid, Fei Chang, Zheng Li, and Mark Mascal. "New bio-based monomers: tuneable polyester properties using branched diols from biomass." Faraday Discussions 202 (2017): 61–77. http://dx.doi.org/10.1039/c7fd00057j.
Повний текст джерелаKundu, Chandan, Saheli Biswas, Mahmud Arman Kibria, and Sankar Bhattacharya. "Thermochemical Conversion of Untreated and Pretreated Biomass for Efficient Production of Levoglucosenone and 5-Chloromethylfurfural in the Presence of an Acid Catalyst." Catalysts 12, no. 2 (February 9, 2022): 206. http://dx.doi.org/10.3390/catal12020206.
Повний текст джерелаGao, Wenhua, Yiqun Li, Zhouyang Xiang, Kefu Chen, Rendang Yang, and Dimitris Argyropoulos. "Correction: Gao, W., et al. Efficient One-Pot Synthesis of 5-Chloromethyl-furfural (CMF) from Carbohydrates in Mild Biphasic Systems. Molecules 2013, 18, 7675-7685." Molecules 19, no. 1 (January 22, 2014): 1370–74. http://dx.doi.org/10.3390/molecules19011370.
Повний текст джерелаPark, Dongwoon, Soohyeon Lee, Jinsung Kim, Ga Yeong Ryu, and Young‐Woong Suh. "5‐(Chloromethyl)Furfural as a Potential Source for Continuous Hydrogenation of 5‐(Hydroxymethyl)Furfural to 2,5‐Bis(Hydroxymethyl)Furan." ChemPlusChem, August 23, 2022. http://dx.doi.org/10.1002/cplu.202200271.
Повний текст джерелаPark, Dongwoon, Soohyeon Lee, Jinsung Kim, Ga Yeong Ryu, and Young‐Woong Suh. "5‐(Chloromethyl)Furfural as a Potential Source for Continuous Hydrogenation of 5‐(Hydroxymethyl)Furfural to 2,5‐Bis(Hydroxymethyl)Furan." ChemPlusChem, August 24, 2022. http://dx.doi.org/10.1002/cplu.202200272.
Повний текст джерелаMiao, Haoqian, Nikolay Shevchenko, Andrew L. Otsuki, and Mark Mascal. "Diversification of the Renewable Furanic Platform via 5‐(Chloromethyl)furfural‐Based Carbon Nucleophiles." ChemSusChem, October 5, 2020. http://dx.doi.org/10.1002/cssc.202001718.
Повний текст джерелаLing, Huitao, Haoqian Miao, Zhiling Cao, and Mark Mascal. "Electrochemical Incorporation of Electrophiles into the Biomass‐derived Platform Molecule 5‐(Chloromethyl)furfural (CMF)." ChemSusChem, December 16, 2022. http://dx.doi.org/10.1002/cssc.202201787.
Повний текст джерелаChen, Binglin, Zheng Li, Yunchao Feng, Weiwei Hao, Yong Sun, Xing Tang, Xianhai Zeng, and Lu Lin. "Green Process for 5‐(Chloromethyl)furfural Production from Biomass in Three‐Constituent Deep Eutectic Solvent." ChemSusChem, January 5, 2021. http://dx.doi.org/10.1002/cssc.202002631.
Повний текст джерелаChen, Binglin, Yunchao Feng, Renjie Huang, Shibo Yang, Zheng Li, Jonathan Sperry, Shuliang Yang, et al. "Efficient Synthesis of the Liquid Fuel 2,5-Dimethylfuran from Biomass Derived 5-(Chloromethyl)Furfural at Room Temperature." SSRN Electronic Journal, 2022. http://dx.doi.org/10.2139/ssrn.4141616.
Повний текст джерелаChen, Binglin, Yunchao Feng, Sen Ma, Weizhen Xie, Guihua Yan, Zheng Li, Jonathan Sperry, et al. "One-pot synthesis of 2,5-bis(hydroxymethyl)furan from biomass derived 5-(chloromethyl)furfural in high yield." Journal of Energy Chemistry, October 2022. http://dx.doi.org/10.1016/j.jechem.2022.10.005.
Повний текст джерелаRojahn, Patrick, Krishna D. P. Nigam, and Frank Schael. "Experimental study and kinetic modeling of continuous flow conversion of fructose to 5-(chloromethyl)furfural using micro- and millistructured coiled flow inverter." Chemical Engineering Journal, July 2022, 138243. http://dx.doi.org/10.1016/j.cej.2022.138243.
Повний текст джерелаLakmini, Loku Mannage N., Athukoralalage Don K. Deshan, Hong Duc Pham, William Doherty, Darryn Rackemann, Deepak P. Dubal, and Lalehvash Moghaddam. "High carbon utilization: 5-(Chloromethyl)furfural (CMF) production from rice by-products and transformation of CMF residues into Li-ion energy storage systems." Journal of Cleaner Production, September 2022, 134082. http://dx.doi.org/10.1016/j.jclepro.2022.134082.
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