His primary areas of study are Catalysis, Organic chemistry, Heterogeneous catalysis, Levulinic acid and Inorganic chemistry. His Catalysis research incorporates elements of Yield, Medicinal chemistry and Alkyl. The various areas that Yao Fu examines in his Medicinal chemistry study include Palladium, Phthalimides, Photochemistry, Oxidative addition and Aryl.
His work in Valerolactone, Homogeneous catalysis, Reaction mechanism, Formic acid and Cellulose are all subfields of Organic chemistry research. In his work, Reductive amination, Amination, Desorption and Oxygenate is strongly intertwined with Ruthenium, which is a subfield of Levulinic acid. His study looks at the intersection of Inorganic chemistry and topics like Carbohydrate with Mesoporous material, Dehydration and Solid acid.
Yao Fu focuses on Catalysis, Organic chemistry, Yield, Medicinal chemistry and Combinatorial chemistry. He combines subjects such as Inorganic chemistry and Photochemistry with his study of Catalysis. His study in Molecule, Furan, Valerolactone, Levulinic acid and Hydrodeoxygenation falls within the category of Organic chemistry.
His study focuses on the intersection of Yield and fields such as Ammonia with connections in the field of Pyrolysis. His Medicinal chemistry study integrates concerns from other disciplines, such as Oxidative addition and Regioselectivity. His work in Oxidative addition addresses subjects such as Aryl, which are connected to disciplines such as Copper catalyzed.
Yao Fu mainly investigates Catalysis, Organic chemistry, Combinatorial chemistry, Yield and Medicinal chemistry. His study in Catalysis is interdisciplinary in nature, drawing from both Furan and Alkyl. His Solvent, Cellulose, Levulinic acid, Reaction mechanism and Fructose study are his primary interests in Organic chemistry.
His Combinatorial chemistry study combines topics in areas such as Nickel, Molecule, Organic synthesis, Aryl and Stereoselectivity. His Yield study also includes fields such as
Catalysis, Organic chemistry, Medicinal chemistry, Palladium and Combinatorial chemistry are his primary areas of study. His Catalysis research includes themes of Yield and Cellulose. His studies deal with areas such as Furan and Lewis acids and bases as well as Yield.
His Medicinal chemistry research is multidisciplinary, incorporating elements of Rhodium, Reactivity and Reaction conditions. Yao Fu has researched Palladium in several fields, including Oxidative addition, Alkyl and Phosphine. His Combinatorial chemistry research integrates issues from Copper catalyzed, Copper, Reagent, Alkyne and Molecule.
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Hydrolysis of cellulose to glucose by solid acid catalysts
Yao-Bing Huang;Yao Fu.
Green Chemistry (2013)
Quantum-Chemical Predictions of Absolute Standard Redox Potentials of Diverse Organic Molecules and Free Radicals in Acetonitrile
Yao Fu;Lei Liu;Hai-Zhu Yu;Yi-Min Wang.
Journal of the American Chemical Society (2005)
Catalytic conversion of biomass-derived carbohydrates into gamma-valerolactone without using an external H2 supply.
Li Deng;Jiang Li;Da-Ming Lai;Yao Fu.
Angewandte Chemie (2009)
Mechanism of Ni-catalyzed selective C-O bond activation in cross-coupling of aryl esters.
Zhe Li;Song-Lin Zhang;Yao Fu;Qing-Xiang Guo.
Journal of the American Chemical Society (2009)
Copper-Catalyzed Decarboxylative Cross-Coupling of Potassium Polyfluorobenzoates with Aryl Iodides and Bromides†
Rui Shang;Rui Shang;Yao Fu;Yao Fu;Yan Wang;Yan Wang;Qing Xu;Qing Xu.
Angewandte Chemie (2009)
First-Principle Predictions of Absolute pKa's of Organic Acids in Dimethyl Sulfoxide Solution
Yao Fu;Lei Liu;Rui-Qiong Li;Rui Liu.
Journal of the American Chemical Society (2004)
Alternative Mechanistic Explanation for Ligand-Dependent Selectivities in Copper-Catalyzed N- and O-Arylation Reactions
Hai-Zhu Yu;Yuan-Ye Jiang;Yao Fu;Lei Liu.
Journal of the American Chemical Society (2010)
Hydrolysis of biomass by magnetic solid acid
Da-ming Lai;Li Deng;Qing-xiang Guo;Yao Fu.
Energy and Environmental Science (2011)
Rhodium-Catalyzed Selective C–H Activation/Olefination of Phenol Carbamates
Tian-Jun Gong;Bin Xiao;Zhao-Jing Liu;Jian Wan.
Organic Letters (2011)
RANEY® Ni catalyzed transfer hydrogenation of levulinate esters to γ-valerolactone at room temperature.
Zhen Yang;Yao-Bing Huang;Qing-Xiang Guo;Yao Fu.
Chemical Communications (2013)
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