Статті в журналах з теми "Deoxydehydration"
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Hacatrjan, Schanth, Lujie Liu, Jianxing Gan, et al. "Titania-supported molybdenum oxide combined with Au nanoparticles as a hydrogen-driven deoxydehydration catalyst of diol compounds." Catalysis Science & Technology 12, no. 7 (2022): 2146–61. http://dx.doi.org/10.1039/d1cy02144c.
Повний текст джерелаTshibalonza, Nelly Ntumba, and Jean-Christophe M. Monbaliu. "Revisiting the deoxydehydration of glycerol towards allyl alcohol under continuous-flow conditions." Green Chemistry 19, no. 13 (2017): 3006–13. http://dx.doi.org/10.1039/c7gc00657h.
Повний текст джерелаXi, Yongjie, Wenqiang Yang, Salai Cheettu Ammal, Jochen Lauterbach, Yomaira Pagan-Torres, and Andreas Heyden. "Mechanistic study of the ceria supported, re-catalyzed deoxydehydration of vicinal OH groups." Catalysis Science & Technology 8, no. 22 (2018): 5750–62. http://dx.doi.org/10.1039/c8cy01782d.
Повний текст джерелаMorris, Danny S., Karlotta van Rees, Massimiliano Curcio, et al. "Deoxydehydration of vicinal diols and polyols catalyzed by pyridinium perrhenate salts." Catalysis Science & Technology 7, no. 23 (2017): 5644–49. http://dx.doi.org/10.1039/c7cy01728f.
Повний текст джерелаWozniak, Bartosz, Yuehui Li, Sergey Tin, and Johannes G. de Vries. "Rhenium-catalyzed deoxydehydration of renewable triols derived from sugars." Green Chemistry 20, no. 19 (2018): 4433–37. http://dx.doi.org/10.1039/c8gc02387e.
Повний текст джерелаTshibalonza, Nelly Ntumba, and Jean-Christophe M. Monbaliu. "The deoxydehydration (DODH) reaction: a versatile technology for accessing olefins from bio-based polyols." Green Chemistry 22, no. 15 (2020): 4801–48. http://dx.doi.org/10.1039/d0gc00689k.
Повний текст джерелаCanale, Valentino, Lucia Tonucci, Mario Bressan, and Nicola d'Alessandro. "Deoxydehydration of glycerol to allyl alcohol catalyzed by rhenium derivatives." Catal. Sci. Technol. 4, no. 10 (2014): 3697–704. http://dx.doi.org/10.1039/c4cy00631c.
Повний текст джерелаChapman, Garry, and Kenneth M. Nicholas. "Vanadium-catalyzed deoxydehydration of glycols." Chemical Communications 49, no. 74 (2013): 8199. http://dx.doi.org/10.1039/c3cc44656e.
Повний текст джерелаSun, Ruiyan, Mingyuan Zheng, Xinsheng Li, et al. "Production of renewable 1,3-pentadiene from xylitol via formic acid-mediated deoxydehydration and palladium-catalyzed deoxygenation reactions." Green Chemistry 19, no. 3 (2017): 638–42. http://dx.doi.org/10.1039/c6gc02868c.
Повний текст джерелаLi, Cui, Qi Zhang, and Yao Fu. "Transition Metal Catalyzed Deoxydehydration of Alcohols." Acta Chimica Sinica 76, no. 7 (2018): 501. http://dx.doi.org/10.6023/a18040138.
Повний текст джерелаDethlefsen, Johannes R., Daniel Lupp, Byung-Chang Oh, and Peter Fristrup. "Molybdenum-Catalyzed Deoxydehydration of Vicinal Diols." ChemSusChem 7, no. 2 (2014): 425–28. http://dx.doi.org/10.1002/cssc.201300945.
Повний текст джерелаXi, Yongjie, Jochen Lauterbach, Yomaira Pagan-Torres, and Andreas Heyden. "Deoxydehydration of 1,4-anhydroerythritol over anatase TiO2(101)-supported ReOx and MoOx." Catalysis Science & Technology 10, no. 11 (2020): 3731–38. http://dx.doi.org/10.1039/d0cy00434k.
Повний текст джерелаDavis, Jacqkis, and Radhey S. Srivastava. "Oxorhenium-catalyzed deoxydehydration of glycols and epoxides." Tetrahedron Letters 55, no. 30 (2014): 4178–80. http://dx.doi.org/10.1016/j.tetlet.2014.05.044.
Повний текст джерелаMichael McClain, J., and Kenneth M. Nicholas. "Elemental Reductants for the Deoxydehydration of Glycols." ACS Catalysis 4, no. 7 (2014): 2109–12. http://dx.doi.org/10.1021/cs500461v.
Повний текст джерелаAhmad, Irshad, Garry Chapman, and Kenneth M. Nicholas. "Sulfite-Driven, Oxorhenium-Catalyzed Deoxydehydration of Glycols." Organometallics 30, no. 10 (2011): 2810–18. http://dx.doi.org/10.1021/om2001662.
Повний текст джерелаBoucher-Jacobs, Camille, and Kenneth M. Nicholas. "Catalytic Deoxydehydration of Glycols with Alcohol Reductants." ChemSusChem 6, no. 4 (2013): 597–99. http://dx.doi.org/10.1002/cssc.201200781.
Повний текст джерелаChapman, Garry Jr, and Kenneth M. Nicholas. "ChemInform Abstract: Vanadium-Catalyzed Deoxydehydration of Glycols." ChemInform 45, no. 2 (2013): no. http://dx.doi.org/10.1002/chin.201402046.
Повний текст джерелаDethlefsen, Johannes R., and Peter Fristrup. "Rhenium-Catalyzed Deoxydehydration of Diols and Polyols." ChemSusChem 8, no. 5 (2014): 767–75. http://dx.doi.org/10.1002/cssc.201402987.
Повний текст джерелаVkuturi, Saidi, Garry Chapman, Irshad Ahmad, and Kenneth M. Nicholas. "Rhenium-Catalyzed Deoxydehydration of Glycols by Sulfite." Inorganic Chemistry 49, no. 11 (2010): 4744–46. http://dx.doi.org/10.1021/ic100467p.
Повний текст джерелаSun, Huimin, Chen Hu, Zhiming Hao, Yajie Zuo, Tianchi Wang, and Chongmin Zhong. "Imidazolinium Perrhenate-Catalyzed Deoxydehydration ofVicinal Diols to Alkenes." Chinese Journal of Organic Chemistry 35, no. 9 (2015): 1904. http://dx.doi.org/10.6023/cjoc201503015.
Повний текст джерелаSandbrink, Lennart, Elisabeth Klindtworth, Husn-Ubayda Islam, Andrew M. Beale, and Regina Palkovits. "ReOx/TiO2: A Recyclable Solid Catalyst for Deoxydehydration." ACS Catalysis 6, no. 2 (2015): 677–80. http://dx.doi.org/10.1021/acscatal.5b01936.
Повний текст джерелаDenning, Alana L., Huong Dang, Zhimin Liu, Kenneth M. Nicholas, and Friederike C. Jentoft. "Deoxydehydration of Glycols Catalyzed by Carbon-Supported Perrhenate." ChemCatChem 5, no. 12 (2013): 3567–70. http://dx.doi.org/10.1002/cctc.201300545.
Повний текст джерелаDeNike, Kayla A., and Stefan M. Kilyanek. "Deoxydehydration of vicinal diols by homogeneous catalysts: a mechanistic overview." Royal Society Open Science 6, no. 11 (2019): 191165. http://dx.doi.org/10.1098/rsos.191165.
Повний текст джерелаBoucher-Jacobs, Camille, and Kenneth M. Nicholas. "Oxo-Rhenium-Catalyzed Deoxydehydration of Polyols with Hydroaromatic Reductants." Organometallics 34, no. 10 (2015): 1985–90. http://dx.doi.org/10.1021/acs.organomet.5b00226.
Повний текст джерелаNavarro, Christine A., and Alex John. "Deoxydehydration using a commercial catalyst and readily available reductant." Inorganic Chemistry Communications 99 (January 2019): 145–48. http://dx.doi.org/10.1016/j.inoche.2018.11.015.
Повний текст джерелаLiu, Peng, and Kenneth M. Nicholas. "Mechanism of Sulfite-Driven, MeReO3-Catalyzed Deoxydehydration of Glycols." Organometallics 32, no. 6 (2013): 1821–31. http://dx.doi.org/10.1021/om301251z.
Повний текст джерелаDavis, Jacqkis, and Radhey S. Srivastava. "ChemInform Abstract: Oxorhenium-Catalyzed Deoxydehydration of Glycols and Epoxides." ChemInform 45, no. 51 (2014): no. http://dx.doi.org/10.1002/chin.201451059.
Повний текст джерелаPetersen, Allan R., and Peter Fristrup. "New Motifs in Deoxydehydration: Beyond the Realms of Rhenium." Chemistry – A European Journal 23, no. 43 (2017): 10235–43. http://dx.doi.org/10.1002/chem.201701153.
Повний текст джерелаDethlefsen, Johannes R., and Peter Fristrup. "ChemInform Abstract: Rhenium-Catalyzed Deoxydehydration of Diols and Polyols." ChemInform 46, no. 19 (2015): no. http://dx.doi.org/10.1002/chin.201519314.
Повний текст джерелаPetersen, Allan R., Lasse B. Nielsen, Johannes R. Dethlefsen, and Peter Fristrup. "Vanadium-Catalyzed Deoxydehydration of Glycerol Without an External Reductant." ChemCatChem 10, no. 4 (2018): 769–78. http://dx.doi.org/10.1002/cctc.201701049.
Повний текст джерелаJefferson, Alana, and Radhey S. Srivastava. "Re-catalyzed deoxydehydration of polyols to olefins using indoline reductants." Polyhedron 160 (March 2019): 268–71. http://dx.doi.org/10.1016/j.poly.2018.11.061.
Повний текст джерелаSharkey, Bryan E., and Friederike C. Jentoft. "Fundamental Insights into Deactivation by Leaching during Rhenium-Catalyzed Deoxydehydration." ACS Catalysis 9, no. 12 (2019): 11317–28. http://dx.doi.org/10.1021/acscatal.9b02806.
Повний текст джерелаde Vicente Poutás, Luis Carlos, Marta Castiñeira Reis, Roberto Sanz, Carlos Silva López, and Olalla Nieto Faza. "A Radical Mechanism for the Vanadium-Catalyzed Deoxydehydration of Glycols." Inorganic Chemistry 55, no. 21 (2016): 11372–82. http://dx.doi.org/10.1021/acs.inorgchem.6b01916.
Повний текст джерелаWu, Di, Yugen Zhang, and Haibin Su. "Mechanistic Study on Oxorhenium-Catalyzed Deoxydehydration and Allylic Alcohol Isomerization." Chemistry - An Asian Journal 11, no. 10 (2016): 1565–71. http://dx.doi.org/10.1002/asia.201600118.
Повний текст джерелаDonnelly, Liam J., Stephen P. Thomas, and Jason B. Love. "Recent Advances in the Deoxydehydration of Vicinal Diols and Polyols." Chemistry – An Asian Journal 14, no. 21 (2019): 3782–90. http://dx.doi.org/10.1002/asia.201901274.
Повний текст джерелаAssaad, Ghadir, Karen Silva Vargas, Benjamin Katryniok, and Marcia Araque. "Simulation Process for Allyl Alcohol Production via Deoxydehydration of Glycerol." ChemEngineering 8, no. 1 (2024): 10. http://dx.doi.org/10.3390/chemengineering8010010.
Повний текст джерелаLupp, Daniel, Niels Johan Christensen, Johannes R. Dethlefsen, and Peter Fristrup. "DFT Study of the Molybdenum-Catalyzed Deoxydehydration of Vicinal Diols." Chemistry - A European Journal 21, no. 8 (2015): 3435–42. http://dx.doi.org/10.1002/chem.201405473.
Повний текст джерелаGopaladasu, Tirupathi V., and Kenneth M. Nicholas. "Carbon Monoxide (CO)- and Hydrogen-Driven, Vanadium-Catalyzed Deoxydehydration of Glycols." ACS Catalysis 6, no. 3 (2016): 1901–4. http://dx.doi.org/10.1021/acscatal.5b02667.
Повний текст джерелаGossett, Justin, and Radhey Srivastava. "Rhenium-catalyzed deoxydehydration of renewable biomass using sacrificial alcohol as reductant." Tetrahedron Letters 58, no. 39 (2017): 3760–63. http://dx.doi.org/10.1016/j.tetlet.2017.08.028.
Повний текст джерелаScioli, Giuseppe, Lucia Tonucci, Pietro Di Profio, Antonio Proto, Raffaele Cucciniello, and Nicola d'Alessandro. "New green route to obtain (bio)-propene through 1,2-propanediol deoxydehydration." Sustainable Chemistry and Pharmacy 17 (September 2020): 100273. http://dx.doi.org/10.1016/j.scp.2020.100273.
Повний текст джерелаMagerat, Alixandre, Sophie Hermans, and Eric M. Gaigneaux. "A novel versatile platform as efficient deoxydehydration (DODH) catalysts: Keggin polyoxometalates." Applied Catalysis B: Environment and Energy 375 (October 2025): 125432. https://doi.org/10.1016/j.apcatb.2025.125432.
Повний текст джерелаLupacchini, Massimiliano, Andrea Mascitti, Valentino Canale, et al. "Deoxydehydration of glycerol in presence of rhenium compounds: reactivity and mechanistic aspects." Catalysis Science & Technology 9, no. 12 (2019): 3036–46. http://dx.doi.org/10.1039/c8cy02478b.
Повний текст джерелаStalpaert, Maxime, та Dirk De Vos. "Stabilizing Effect of Bulky β-Diketones on Homogeneous Mo Catalysts for Deoxydehydration". ACS Sustainable Chemistry & Engineering 6, № 9 (2018): 12197–204. http://dx.doi.org/10.1021/acssuschemeng.8b02532.
Повний текст джерелаJang, Jun Hee, Hyuntae Sohn, Jeffrey Camacho-Bunquin, et al. "Deoxydehydration of Biomass-Derived Polyols with a Reusable Unsupported Rhenium Nanoparticles Catalyst." ACS Sustainable Chemistry & Engineering 7, no. 13 (2019): 11438–47. http://dx.doi.org/10.1021/acssuschemeng.9b01253.
Повний текст джерелаTazawa, Shuhei, Nobuhiko Ota, Masazumi Tamura, Yoshinao Nakagawa, Kazu Okumura, and Keiichi Tomishige. "Deoxydehydration with Molecular Hydrogen over Ceria-Supported Rhenium Catalyst with Gold Promoter." ACS Catalysis 6, no. 10 (2016): 6393–97. http://dx.doi.org/10.1021/acscatal.6b01864.
Повний текст джерелаJiang, Yuan-Ye, Ju-Long Jiang, and Yao Fu. "Mechanism of Vanadium-Catalyzed Deoxydehydration of Vicinal Diols: Spin-Crossover-Involved Processes." Organometallics 35, no. 19 (2016): 3388–96. http://dx.doi.org/10.1021/acs.organomet.6b00602.
Повний текст джерелаGalindo, Agustín. "DFT Studies on the Mechanism of the Vanadium-Catalyzed Deoxydehydration of Diols." Inorganic Chemistry 55, no. 5 (2016): 2284–89. http://dx.doi.org/10.1021/acs.inorgchem.5b02649.
Повний текст джерелаLiu, Shuo, Aysegul Senocak, Jessica L. Smeltz, et al. "Mechanism of MTO-Catalyzed Deoxydehydration of Diols to Alkenes Using Sacrificial Alcohols." Organometallics 32, no. 11 (2013): 3210–19. http://dx.doi.org/10.1021/om400127z.
Повний текст джерелаVargas, Karen Silva, Jeremie Zaffran, Marcia Araque, Masahiro Sadakane, and Benjamin Katryniok. "Deoxydehydration of glycerol to allyl alcohol catalysed by ceria-supported rhenium oxide." Molecular Catalysis 535 (January 2023): 112856. http://dx.doi.org/10.1016/j.mcat.2022.112856.
Повний текст джерелаLi, Jing, Martin Lutz, and Robertus J. M. Klein Gebbink. "A Cp‐based Molybdenum Catalyst for the Deoxydehydration of Biomass‐derived Diols." ChemCatChem 12, no. 24 (2020): 6356–65. http://dx.doi.org/10.1002/cctc.202001115.
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