Γ-Valerolacton (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Γ-Valerolacton" in German language version.

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  • K. Yan, Y. Yang, J. Chai, Y. Lu: Catalytic reactions of gamma-valerolactone: A platform to fuels and value-added chemicals. In: Appl. Catal. B: Environmental. Band 179, 2015, S. 292–305, doi:10.1016/j.apcatb.2015.04.030.
  • D.M. Alonso, S.G. Wettstein, J.A. Dumesic: Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass. In: Green Chem. Band 15, 2013, S. 584–595, doi:10.1039/C3GC37065H.
  • A. Messerschmidt: Untersuchungen über die ungesättigten Säuren. Ueber die Allylessigsäure und das Valerolacton. In: Justus Liebigs Ann. Chem. Band 208, Nr. 1–2, 1881, S. 92–104, doi:10.1002/jlac.18812080107.
  • K. Komeyama, Y. Mieno, S. Yukawa, T. Morimoto, K. Takaki: Cationic iron-catalyzed addition of carboxylic acids to olefins. In: Chem. Lett. Band 36, Nr. 6, 2007, S. 752–753, doi:10.1246/cl.2007.752.
  • J.H. Helberger, S. Ulabay, H. Civelekoglu: Ein einfaches Verfahren zur Gewinnung von α-Angelicalacton und über die hydrierende Spaltung sauerstoffhaltiger Ringe. In: Justus Liebigs Ann. Chem. Band 561, Nr. 3, 1949, S. 215–220, doi:10.1002/jlac.19495610307.
  • A. Díaz-Rodríguez, I. Lavandera, S. Kanbak-Aksu, R.A. Sheldon, V. Gotor, V. Gotor-Fernández: From Diols to Lactones under Aerobic Conditions using a Laccase/TEMPO Catalytic System in Aqueous Medium. In: Adv. Synth. Catal. Band 354, 2012, S. 3405–3408, doi:10.1002/adsc.201200892.
  • N. Kim, M.S. Kwon, C.M. Park, J. Park: One pot synthesis of recyclable palladium catalysts for hydrogenations and carbon-carbon coupling reactions. In: Tetrahedron Lett. Band 45, Nr. 38, 2004, S. 7057–7059, doi:10.1016/tetlet.2004.07.126.
  • M.J. Climent, A. Corma, S. Iborra: Conversion of biomass platform molecules into fuel additives and liquid hydrocarbon fuel. In: Green Chem. Band 16, 2014, S. 516–547, doi:10.1039/c3gc41492b.
  • W. Wright, R. Palkovits: Development of heterogeneous catalysts for the conversion of levulinic acid into gamma-valerolactone. In: Chemsuschem. Band 5, 2012, S. 1657–1667, doi:10.1002/cssc.201200111.
  • H.A. Schuette, R.W. Thomas: Normal valerolactone. III. Its preparation by the catalytic reduction of levulinic acid with hydrogen in the presence of platinum oxide. In: J. Am. Chem. Soc. Band 52, Nr. 7, 1930, S. 3010–3012, doi:10.1021/ja01370a069.
  • X.-L. Du, L. He, S. Zhao, Y.-M. Liu, Y. Cao, H.-Y. He, K.-N. Fan: Hydrogen-independent reductive transformation of carbohydrate biomass into γ-valerolactone and pyrrolidone derivatives with supported gold catalysts. In: Angew. Chem. Band 123, Nr. 34, 2011, S. 7961–7965, doi:10.1002/ange.201100102.
  • D.M. Alonso, J.M.R. Gallo, M.A. Mellmer, S.G. Wettstein, J.A. Dumesic: Direct conversion of cellulose to levulinic acid and gamma-valerolactone using solid acid catalysts. In: Catal. Sci. Technol. Band 3, 2013, S. 925–931, doi:10.1039/C2CY20689G.
  • V.S. Java, M. Sudharkar, S.N. Kumar, A. Venugopal: Selective hydrogenation of levulinic acid to γ-valerolactone over a Ru/Mg-LaO catalyst. In: RSC Adv. Band 5, 2015, S. 9044–9049, doi:10.1039/C4RA16557H.
  • W. Luo, M. Sankar, A.M. Beale, Q. He, C.J. Kiely, P.C.A. Bruijnincx, B.M. Weckhuysen: High performing and stable supported nano-alloys for the catalytic hydrogenation of levulinic acid to γ-valerolactone. In: Nature Commun. Band 5, Nr. 6540, 2015, doi:10.1038/ncomms7540.
  • V. Fábros, L.T. Mika, I.T. Horváth: Selective conversion of levulinic and formic acids to γ-valerolactone with the Shvo catalyst. In: Organometallics. Band 33, Nr. 1, 2014, S. 181–187, doi:10.1021/om400938h.
  • S.G. Wettstein, D.M. Alonso, Y. Chong, J.A. Dumesic: Production of levulinic acid and gamma-valerolactone (GVL) from cellulose using GVL as solvent in biphasic systems. In: Energy Environ. Sci. Band 5, 2012, S. 8199–8203, doi:10.1039/C2EE22111J.
  • V. Molinari, M. Antonietti, D. Esposito: An integrated strategy for the conversion of cellulosic biomass into gamma-valerolactone. In: Catal. Sci. Technol. Band 4, Nr. 10, 2014, S. 3626–3630, doi:10.1039/c4cy00717d.
  • József M. Tukacs, Bálint Fridrich, Gábor Dibó, Edit Székely, László T. Mika: Direct asymmetric reduction of levulinic acid to gamma-valerolactone: synthesis of a chiral platform molecule. In: Green Chemistry. 17, 2015, S. 5189, doi:10.1039/C5GC01099C.
  • H. Andresen-Streichert, H. Jungen, A. Gehl, A. Müller, S. Iwersen-Bergmann: Uptake of Gamma-Valerolactone—Detection of Gamma-Hydroxyvaleric Acid in Human Urine Samples. In: J. Analyt. Toxicol. Band 37, Nr. 4, 2013, S. 250–254, doi:10.1093/jat/bkt013.
  • I.T. Horváth, H. Mehdi, V. Fábos, L. Boda, L.T. Mika: γ-Valerolactone, a sustainable liquid for energy and carbon-based chemicals. In: Green Chem. Band 10, 2008, S. 238–242, doi:10.1039/B712863K.
  • J.S. Luterbacher, J.M. Rand, D.M. Alonso, J. Han, J.T. Youngquist, C.T. Maravelias, B.F. Pfleger, J.A. Dumesic: Nonenzymatic sugar production from biomass using biomass-derived γ-valerolactone. In: Science. Band 343, Nr. 6168, 2014, S. 277–280, doi:10.1126/science.1246748.
  • M. Gagliardi, F. Di Michele, B. Mazzolai, A. Bifone: Chemical synthesis of a biodegradable PEGylated copolymer from ε-caprolactone and γ-valerolactone: evaluation of reaction and functional properties. In: J. Polym. Res. Band 22:17, 2015, S. 1–12, doi:10.1007/s10965-015-0661-2.
  • Á. Bereczky, K. Lukács, M. Farkas, S. Dóbé: Effect of γ-Valerolactone Blending on Engine Performance, Combustion Characteristics and Exhaust Emissions in a Diesel Engine. In: Natural Resources. Band 5, 2014, S. 177–191, doi:10.4236/nr.2014.55017.

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  • Patent US2809203: Method of converting levulinic acid into alpha angelica lactone. Angemeldet am 14. Mai 1953, veröffentlicht am 8. Oktober 1957, Anmelder: Heyden Newport Chemical Co., Erfinder: R.H. Leonard.
  • Patent US2368366: Process for the production of lactones. Angemeldet am 21. August 1942, veröffentlicht am 30. Januar 1945, Anmelder: Monsanto Chemical Co., Erfinder: L.P. Kyrides, W. Groves, J.K. Craver.

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