Vitamin B1-Catalyzed Acetoin Formation from Acetaldehyde: A Key Step for Upgrading Bioethanol to Bulk C4Chemicals
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Vitamin B1-Catalyzed Acetoin Formation from Acetaldehyde: A Key Step for Upgrading Bioethanol to Bulk C4Chemicals
Authors
Keywords
-
Journal
ChemSusChem
Volume 7, Issue 9, Pages 2423-2426
Publisher
Wiley
Online
2014-07-19
DOI
10.1002/cssc.201402396
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Highly Efficient Chemical Process To Convert Mucic Acid into Adipic Acid and DFT Studies of the Mechanism of the Rhenium-Catalyzed Deoxydehydration
- (2014) Xiukai Li et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Catalytic Conversion of Ethanol into an Advanced Biofuel: Unprecedented Selectivity forn-Butanol
- (2013) George R. M. Dowson et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Replacing Phosphorus with Sulfur for the Efficient Hydrogenation of Esters
- (2013) Denis Spasyuk et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Expanding the Scope of Biomass-Derived Chemicals through Tandem Reactions Based on Oxorhenium-Catalyzed Deoxydehydration
- (2013) Mika Shiramizu et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Deoxydehydration of Glycols Catalyzed by Carbon-Supported Perrhenate
- (2013) Alana L. Denning et al. ChemCatChem
- Catalytic Deoxydehydration of Glycols with Alcohol Reductants
- (2013) Camille Boucher-Jacobs et al. ChemSusChem
- Chemocatalytic Conversion of Ethanol into Butadiene and Other Bulk Chemicals
- (2013) Carlo Angelici et al. ChemSusChem
- Selective Acceptorless Conversion of Primary Alcohols to Acetals and Dihydrogen Catalyzed by the Ruthenium(II) Complex Ru(PPh3)2(NCCH3)2(SO4)
- (2012) Elizaveta Kossoy et al. ADVANCED SYNTHESIS & CATALYSIS
- Deoxygenation of Biomass-Derived Feedstocks: Oxorhenium-Catalyzed Deoxydehydration of Sugars and Sugar Alcohols
- (2012) Mika Shiramizu et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Potential of bioethanol as a chemical building block for biorefineries: Preliminary sustainability assessment of 12 bioethanol-based products
- (2012) John A. Posada et al. BIORESOURCE TECHNOLOGY
- Catalytic study of the conversion of ethanol into 1,3-butadiene
- (2012) E.V. Makshina et al. CATALYSIS TODAY
- Rhenium-Catalyzed Transfer Hydrogenation and Deoxygenation of Biomass-Derived Polyols to Small and Useful Organics
- (2012) Jing Yi et al. ChemSusChem
- Design and synthesis of novel chiral dihydroimidazolium cyclophanes as N-heterocyclic carbene precatalysts
- (2012) Ting Lu et al. TETRAHEDRON LETTERS
- One-Pot Liquid-Phase Catalytic Conversion of Ethanol to 1-Butanol over Aluminium Oxide—The Effect of the Active Metal on the Selectivity
- (2012) Toni Riittonen et al. Catalysts
- Efficient Hydrogen Production from Alcohols under Mild Reaction Conditions
- (2011) Martin Nielsen et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Selective synthesis of 1-butanol from ethanol over strontium phosphate hydroxyapatite catalysts
- (2011) Shuhei Ogo et al. APPLIED CATALYSIS A-GENERAL
- Mg and Al mixed oxides and the synthesis of n-butanol from ethanol
- (2011) Débora L. Carvalho et al. APPLIED CATALYSIS A-GENERAL
- Ethanol catalytic condensation over Mg–Al mixed oxides derived from hydrotalcites
- (2010) Marta León et al. CATALYSIS TODAY
- The Catalytic Valorization of Lignin for the Production of Renewable Chemicals
- (2010) Joseph Zakzeski et al. CHEMICAL REVIEWS
- Catalytic valorization of bioethanol over Cu-Mg-Al mixed oxide catalysts
- (2009) Ioan-Cezar Marcu et al. CATALYSIS TODAY
- Comparative characterisation of thiamin diphosphate-dependent decarboxylases
- (2009) Dörte Gocke et al. JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC
- Catalytic Conversion of Biomass: Challenges and Issues
- (2008) Pierre Gallezot ChemSusChem
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started