Heterogeneous palladium-catalysed Catellani reaction in biomass-derived γ-valerolactone
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Title
Heterogeneous palladium-catalysed Catellani reaction in biomass-derived γ-valerolactone
Authors
Keywords
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Journal
GREEN CHEMISTRY
Volume 18, Issue 18, Pages 5025-5030
Publisher
Royal Society of Chemistry (RSC)
Online
2016-06-10
DOI
10.1039/c6gc01393g
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Note: Only part of the references are listed.- Synthesis of γ-Valerolactone from Carbohydrates and its Applications
- (2016) Zehui Zhang ChemSusChem
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- (2015) Giacomo Strappaveccia et al. GREEN CHEMISTRY
- Ligand-Enabled Meta-C–H Alkylation and Arylation Using a Modified Norbornene
- (2015) Peng-Xiang Shen et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Simple Amine-Directed Meta-Selective C–H Arylation via Pd/Norbornene Catalysis
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- Palladium-Catalyzed Acylation/Alkenylation of Aryl Iodide: A Domino Approach Based on the Catellani–Lautens Reaction
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- (2014) Tehetena Mesganaw et al. ORGANIC PROCESS RESEARCH & DEVELOPMENT
- Catalytic Conversion of Fructose, Glucose, and Sucrose to 5-(Hydroxymethyl)furfural and Levulinic and Formic Acids in γ-Valerolactone As a Green Solvent
- (2014) Long Qi et al. ACS Catalysis
- γ-Valerolactone as a Renewable Dipolar Aprotic Solvent Deriving from Biomass Degradation for the Hiyama Reaction
- (2014) Ermal Ismalaj et al. ACS Sustainable Chemistry & Engineering
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- (2009) Lutz Ackermann et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
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- Catalytic Direct Arylations in Polyethylene Glycol (PEG): Recyclable Palladium(0) Catalyst for C−H Bond Cleavages in the Presence of Air
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- Catalytic Sequential Reactions Involving Palladacycle-Directed Aryl Coupling Steps
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- γ-Valerolactone—a sustainable liquid for energy and carbon-based chemicals
- (2007) István T. Horváth et al. GREEN CHEMISTRY
- Green chemistry tools to influence a medicinal chemistry and research chemistry based organisation
- (2007) Kim Alfonsi et al. GREEN CHEMISTRY
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