His primary areas of study are Organic chemistry, Catalysis, Combinatorial chemistry, Stereoselectivity and Molecule. His work on Chlorine expands to the thematically related Catalysis. His Combinatorial chemistry research is multidisciplinary, relying on both Photocatalysis, Electrocatalyst, Annulation, Cationic polymerization and Radical.
His work deals with themes such as Amination, Medicinal chemistry, Regioselectivity, Bond formation and Acetonitrile, which intersect with Stereoselectivity. In his study, Tetrabutylammonium iodide is inextricably linked to Alkyl, which falls within the broad field of Medicinal chemistry. The Stereoisomerism, Supramolecular polymers and Calixarene research Guigen Li does as part of his general Molecule study is frequently linked to other disciplines of science, such as Förster resonance energy transfer, therefore creating a link between diverse domains of science.
Guigen Li focuses on Catalysis, Organic chemistry, Combinatorial chemistry, Medicinal chemistry and Stereoselectivity. His Catalysis research is multidisciplinary, incorporating perspectives in Vicinal, Halogenation and Nitrogen. His works in Enantioselective synthesis, Electrophile, Stereoisomerism, Molecule and Aldol reaction are all subjects of inquiry into Organic chemistry.
His studies deal with areas such as Chirality, Stereochemistry, Lithium and Imine as well as Enantioselective synthesis. His Combinatorial chemistry research incorporates elements of Reagent, Functional group, Domino, Aryl and Cascade reaction. The concepts of his Medicinal chemistry study are interwoven with issues in Cycloaddition, Lewis acids and bases, Adduct, Alkyl and Copper.
His primary scientific interests are in Catalysis, Combinatorial chemistry, Medicinal chemistry, Chirality and Enantioselective synthesis. The Catalysis study combines topics in areas such as Functional group and Alkyl. His work carried out in the field of Combinatorial chemistry brings together such families of science as Reagent, Regioselectivity, Electrochemistry, Nucleophile and Stereoselectivity.
His Medicinal chemistry research includes themes of Cobalt, Metal and Carbene. His Chirality study also includes
Guigen Li spends much of his time researching Catalysis, Combinatorial chemistry, Electrochemistry, Medicinal chemistry and Chemoselectivity. He interconnects Triple bond, Cleavage and Metal in the investigation of issues within Catalysis. Guigen Li combines subjects such as Ligand, Surface modification and Palladium with his study of Combinatorial chemistry.
His research integrates issues of Sodium acetate, Primary, Carboxylate, Azide and Iridium in his study of Medicinal chemistry. Guigen Li combines subjects such as Carbonate, Anode, Domino, Oxygen evolution and Caesium with his study of Chemoselectivity. Amination is a subfield of Organic chemistry that Guigen Li explores.
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Catalytic Asymmetric Aminohydroxylation (AA) of Olefins
Guigen Li;Han‐Ting Chang;K. Barry Sharpless.
Angewandte Chemie (1996)
Multicomponent Reactions for the Synthesis of Heterocycles
Bo Jiang;Trideep Rajale;Walter Wever;Shu-Jiang Tu.
Chemistry-an Asian Journal (2010)
Vicinal Diamino Functionalities as Privileged Structural Elements in Biologically Active Compounds and Exploitation of their Synthetic Chemistry
S. R. S. Saibabu Kotti;Cody Timmons;Guigen Li.
Chemical Biology & Drug Design (2006)
Cobalt-catalysed site-selective intra- and intermolecular dehydrogenative amination of unactivated sp(3) carbons.
Xuesong Wu;Ke Yang;Yan Zhao;Hao Sun.
Nature Communications (2015)
Four-Component Domino Reaction Leading to Multifunctionalized Quinazolines
Bo Jiang;Shu-Jiang Tu;Parminder Kaur;Walter Wever.
Journal of the American Chemical Society (2009)
N‐Halocarbamate Salts Lead to More Efficient Catalytic Asymmetric Aminohydroxylation
Guigen Li;Hubert H. Angert;K. Barry Sharpless.
Angewandte Chemie (1996)
A Novel Electrophilic Diamination Reaction of Alkenes.
Guigen Li;Han-Xun Wei;Sun Hee Kim;Michael D. Carducci.
Angewandte Chemie (2001)
Recent Development of Regio- and Stereoselective Aminohalogenation Reaction of Alkenes
Guigen Li;S. R. S. Saibabu Kotti;Cody Timmons.
European Journal of Organic Chemistry (2007)
New multicomponent domino reactions (MDRs) in water: highly chemo-, regio- and stereoselective synthesis of spiro{[1,3]dioxanopyridine}-4,6-diones and pyrazolo[3,4-b]pyridines
Ning Ma;Bo Jiang;Ge Zhang;Shu-Jiang Tu.
Green Chemistry (2010)
Catalytic Dual 1,1-H-Abstraction/Insertion for Domino Spirocyclizations
Jiang-Kai Qiu;Bo Jiang;Yi-Long Zhu;Wen-Juan Hao.
Journal of the American Chemical Society (2015)
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