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Journal articles on the topic 'Deoxydehydration'

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Author: Grafiati

Published: 12 May 2022

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1

Hacatrjan, Schanth, Lujie Liu, Jianxing Gan, Yoshinao Nakagawa, Ji Cao, Mizuho Yabushita, Masazumi Tamura, and Keiichi Tomishige. "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.

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2

Tshibalonza, 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.

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3

Xi, 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.

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4

Morris, Danny S., Karlotta van Rees, Massimiliano Curcio, Mirza Cokoja, Fritz E. Kühn, Fernanda Duarte, and Jason B. Love. "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.

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5

Wozniak, 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.

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6

Tshibalonza, 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.

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7

Chapman, Garry, and Kenneth M. Nicholas. "Vanadium-catalyzed deoxydehydration of glycols." Chemical Communications 49, no. 74 (2013): 8199. http://dx.doi.org/10.1039/c3cc44656e.

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8

Canale, 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.

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9

Li, 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.

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10

Dethlefsen, Johannes R., Daniel Lupp, Byung-Chang Oh, and Peter Fristrup. "Molybdenum-Catalyzed Deoxydehydration of Vicinal Diols." ChemSusChem 7, no. 2 (January 7, 2014): 425–28. http://dx.doi.org/10.1002/cssc.201300945.

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11

Sun, Ruiyan, Mingyuan Zheng, Xinsheng Li, Jifeng Pang, Aiqin Wang, Xiaodong Wang, and Tao Zhang. "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.

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Abstract:

A two-step synthetic approach for the production of renewable 1,3-pentadiene was reported: xylitol deoxydehydration (DODH) by formic acid to 2,4-pentadien-1-ol, 1-formate (2E), followed by deoxygenation to 1,3-pentadiene over Pd/C.

12

Xi, 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.

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Abstract:

Heterogeneously catalyzed deoxydehydration (DODH) ordinarily occurs over oxide supported ReO_x sites. A comparably high activity of MoO_x/TiO₂(101) suggests that it is a promising low-cost DODH catalyst that can replace Re-based catalysts.

13

Vkuturi, Saidi, Garry Chapman, Irshad Ahmad, and Kenneth M. Nicholas. "Rhenium-Catalyzed Deoxydehydration of Glycols by Sulfite." Inorganic Chemistry 49, no. 11 (June 7, 2010): 4744–46. http://dx.doi.org/10.1021/ic100467p.

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14

Davis, Jacqkis, and Radhey S. Srivastava. "Oxorhenium-catalyzed deoxydehydration of glycols and epoxides." Tetrahedron Letters 55, no. 30 (July 2014): 4178–80. http://dx.doi.org/10.1016/j.tetlet.2014.05.044.

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15

Michael McClain, J., and Kenneth M. Nicholas. "Elemental Reductants for the Deoxydehydration of Glycols." ACS Catalysis 4, no. 7 (June 2, 2014): 2109–12. http://dx.doi.org/10.1021/cs500461v.

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16

Dethlefsen, Johannes R., and Peter Fristrup. "Rhenium-Catalyzed Deoxydehydration of Diols and Polyols." ChemSusChem 8, no. 5 (December 4, 2014): 767–75. http://dx.doi.org/10.1002/cssc.201402987.

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17

Chapman, Garry Jr, and Kenneth M. Nicholas. "ChemInform Abstract: Vanadium-Catalyzed Deoxydehydration of Glycols." ChemInform 45, no. 2 (December 19, 2013): no. http://dx.doi.org/10.1002/chin.201402046.

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18

Boucher-Jacobs, Camille, and Kenneth M. Nicholas. "Catalytic Deoxydehydration of Glycols with Alcohol Reductants." ChemSusChem 6, no. 4 (March 26, 2013): 597–99. http://dx.doi.org/10.1002/cssc.201200781.

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19

Ahmad, Irshad, Garry Chapman, and Kenneth M. Nicholas. "Sulfite-Driven, Oxorhenium-Catalyzed Deoxydehydration of Glycols." Organometallics 30, no. 10 (May 23, 2011): 2810–18. http://dx.doi.org/10.1021/om2001662.

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20

Sun, 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.

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21

Sandbrink, 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 (December 29, 2015): 677–80. http://dx.doi.org/10.1021/acscatal.5b01936.

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22

Denning, 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 (August 13, 2013): 3567–70. http://dx.doi.org/10.1002/cctc.201300545.

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23

DeNike, Kayla A., and Stefan M. Kilyanek. "Deoxydehydration of vicinal diols by homogeneous catalysts: a mechanistic overview." Royal Society Open Science 6, no. 11 (November 2019): 191165. http://dx.doi.org/10.1098/rsos.191165.

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Abstract:

Deoxydehydration (DODH) is an important reaction for the upconversion of biomass-derived polyols to commodity chemicals such as alkenes and dienes. DODH can be performed by a variety of early metal-oxo catalysts incorporating Re, Mo and V. The varying reduction methods used in the DODH catalytic cycle impact the product distribution, reaction mechanism and the overall yield of the reaction. This review surveys the reduction methods commonly used in homogeneous DODH catalyst systems and their impacts on yield and reaction conditions.

24

Boucher-Jacobs, Camille, and Kenneth M. Nicholas. "Oxo-Rhenium-Catalyzed Deoxydehydration of Polyols with Hydroaromatic Reductants." Organometallics 34, no. 10 (May 8, 2015): 1985–90. http://dx.doi.org/10.1021/acs.organomet.5b00226.

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25

Dethlefsen, Johannes R., and Peter Fristrup. "ChemInform Abstract: Rhenium-Catalyzed Deoxydehydration of Diols and Polyols." ChemInform 46, no. 19 (April 23, 2015): no. http://dx.doi.org/10.1002/chin.201519314.

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26

Petersen, Allan R., and Peter Fristrup. "New Motifs in Deoxydehydration: Beyond the Realms of Rhenium." Chemistry – A European Journal 23, no. 43 (June 19, 2017): 10235–43. http://dx.doi.org/10.1002/chem.201701153.

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27

Davis, Jacqkis, and Radhey S. Srivastava. "ChemInform Abstract: Oxorhenium-Catalyzed Deoxydehydration of Glycols and Epoxides." ChemInform 45, no. 51 (December 4, 2014): no. http://dx.doi.org/10.1002/chin.201451059.

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28

Liu, Peng, and Kenneth M. Nicholas. "Mechanism of Sulfite-Driven, MeReO3-Catalyzed Deoxydehydration of Glycols." Organometallics 32, no. 6 (February 26, 2013): 1821–31. http://dx.doi.org/10.1021/om301251z.

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29

Navarro, 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.

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30

Petersen, Allan R., Lasse B. Nielsen, Johannes R. Dethlefsen, and Peter Fristrup. "Vanadium-Catalyzed Deoxydehydration of Glycerol Without an External Reductant." ChemCatChem 10, no. 4 (January 8, 2018): 769–78. http://dx.doi.org/10.1002/cctc.201701049.

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31

de 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 (October 14, 2016): 11372–82. http://dx.doi.org/10.1021/acs.inorgchem.6b01916.

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32

Jefferson, 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.

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33

Sharkey, Bryan E., and Friederike C. Jentoft. "Fundamental Insights into Deactivation by Leaching during Rhenium-Catalyzed Deoxydehydration." ACS Catalysis 9, no. 12 (October 24, 2019): 11317–28. http://dx.doi.org/10.1021/acscatal.9b02806.

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34

Donnelly, 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 (October 22, 2019): 3782–90. http://dx.doi.org/10.1002/asia.201901274.

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35

Lupp, 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 (January 14, 2015): 3435–42. http://dx.doi.org/10.1002/chem.201405473.

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36

Wu, Di, Yugen Zhang, and Haibin Su. "Mechanistic Study on Oxorhenium-Catalyzed Deoxydehydration and Allylic Alcohol Isomerization." Chemistry - An Asian Journal 11, no. 10 (April 9, 2016): 1565–71. http://dx.doi.org/10.1002/asia.201600118.

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37

Gopaladasu, Tirupathi V., and Kenneth M. Nicholas. "Carbon Monoxide (CO)- and Hydrogen-Driven, Vanadium-Catalyzed Deoxydehydration of Glycols." ACS Catalysis 6, no. 3 (February 18, 2016): 1901–4. http://dx.doi.org/10.1021/acscatal.5b02667.

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38

Gossett, Justin, and Radhey Srivastava. "Rhenium-catalyzed deoxydehydration of renewable biomass using sacrificial alcohol as reductant." Tetrahedron Letters 58, no. 39 (September 2017): 3760–63. http://dx.doi.org/10.1016/j.tetlet.2017.08.028.

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39

Scioli, 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.

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40

Tazawa, 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 (August 29, 2016): 6393–97. http://dx.doi.org/10.1021/acscatal.6b01864.

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41

Jang, Jun Hee, Hyuntae Sohn, Jeffrey Camacho-Bunquin, Dali Yang, Chan Y. Park, Massimiliano Delferro, and Mahdi M. Abu-Omar. "Deoxydehydration of Biomass-Derived Polyols with a Reusable Unsupported Rhenium Nanoparticles Catalyst." ACS Sustainable Chemistry & Engineering 7, no. 13 (May 29, 2019): 11438–47. http://dx.doi.org/10.1021/acssuschemeng.9b01253.

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42

Stalpaert, Maxime, and Dirk De Vos. "Stabilizing Effect of Bulky β-Diketones on Homogeneous Mo Catalysts for Deoxydehydration." ACS Sustainable Chemistry & Engineering 6, no. 9 (July 25, 2018): 12197–204. http://dx.doi.org/10.1021/acssuschemeng.8b02532.

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43

Galindo, Agustín. "DFT Studies on the Mechanism of the Vanadium-Catalyzed Deoxydehydration of Diols." Inorganic Chemistry 55, no. 5 (February 22, 2016): 2284–89. http://dx.doi.org/10.1021/acs.inorgchem.5b02649.

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44

Lupacchini, Massimiliano, Andrea Mascitti, Valentino Canale, Lucia Tonucci, Evelina Colacino, Maurizio Passacantando, Alessandro Marrone, and Nicola d'Alessandro. "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.

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45

Jiang, Yuan-Ye, Ju-Long Jiang, and Yao Fu. "Mechanism of Vanadium-Catalyzed Deoxydehydration of Vicinal Diols: Spin-Crossover-Involved Processes." Organometallics 35, no. 19 (September 20, 2016): 3388–96. http://dx.doi.org/10.1021/acs.organomet.6b00602.

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46

Qu, Shuanglin, Yanfeng Dang, Mingwei Wen, and Zhi-Xiang Wang. "Mechanism of the Methyltrioxorhenium-Catalyzed Deoxydehydration of Polyols: A New Pathway Revealed." Chemistry - A European Journal 19, no. 12 (February 18, 2013): 3827–32. http://dx.doi.org/10.1002/chem.201204001.

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47

Sandbrink, Lennart, Klaus Beckerle, Isabell Meiners, Rebecca Liffmann, Khosrow Rahimi, Jun Okuda, and Regina Palkovits. "Supported Molybdenum Catalysts for the Deoxydehydration of 1,4-Anhydroerythritol into 2,5-Dihydrofuran." ChemSusChem 10, no. 7 (March 2, 2017): 1375–79. http://dx.doi.org/10.1002/cssc.201700010.

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48

Li, 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 (November 4, 2020): 6356–65. http://dx.doi.org/10.1002/cctc.202001115.

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49

Liu, Shuo, Aysegul Senocak, Jessica L. Smeltz, Linan Yang, Benjamin Wegenhart, Jing Yi, Hilkka I. Kenttämaa, Elon A. Ison, and Mahdi M. Abu-Omar. "Mechanism of MTO-Catalyzed Deoxydehydration of Diols to Alkenes Using Sacrificial Alcohols." Organometallics 32, no. 11 (May 21, 2013): 3210–19. http://dx.doi.org/10.1021/om400127z.

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50

Dethlefsen, Johannes R., and Peter Fristrup. "In Situ Spectroscopic Investigation of the Rhenium-Catalyzed Deoxydehydration of Vicinal Diols." ChemCatChem 7, no. 7 (March 10, 2015): 1184–96. http://dx.doi.org/10.1002/cctc.201403012.

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