Mechanism of Glucose Isomerization Using a Solid Lewis Acid Catalyst in Water
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- 20 October 2010
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 49 (47), 8954-8957
- https://doi.org/10.1002/anie.201004689
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Metal Ion Roles and the Movement of Hydrogen during Reaction Catalyzed by D-Xylose Isomerase: A Joint X-Ray and Neutron Diffraction StudyStructure, 2010
- Conversion of Sugars to Lactic Acid Derivatives Using Heterogeneous Zeotype CatalystsScience, 2010
- Tin-containing zeolites are highly active catalysts for the isomerization of glucose in waterProceedings of the National Academy of Sciences, 2010
- Water Resistant, Catalytically Active Nb and Ta Isolated Lewis Acid Sites, Homogeneously Distributed by Direct Synthesis in a Beta ZeoliteThe Journal of Physical Chemistry C, 2009
- Katalytische Flüssigphasenumwandlung oxygenierter Kohlenwasserstoffe aus Biomasse zu Treibstoffen und Rohstoffen für die ChemiewirtschaftAngewandte Chemie, 2007
- Mechanism of the Meerwein−Ponndorf−Verley−Oppenauer (MPVO) Redox Equilibrium on Sn− and Zr−Beta Zeolite CatalystsThe Journal of Physical Chemistry B, 2006
- Determination of the catalytically active oxidation Lewis acid sites in Sn-beta zeolites, and their optimisation by the combination of theoretical and experimental studiesJournal of Catalysis, 2005
- Sn-Beta zeolite as diastereoselective water-resistant heterogeneous Lewis-acid catalyst for carbon–carbon bond formation in the intramolecular carbonyl–ene reactionChemical Communications, 2004
- Water-resistant solid Lewis acid catalysts: Meerwein–Ponndorf–Verley and Oppenauer reactions catalyzed by tin-beta zeoliteJournal of Catalysis, 2003
- Al-Free Sn-Beta Zeolite as a Catalyst for the Selective Reduction of Carbonyl Compounds (Meerwein−Ponndorf−Verley Reaction)Journal of the American Chemical Society, 2002