His main research concerns Organic chemistry, Catalysis, Enantioselective synthesis, Combinatorial chemistry and Organocatalysis. His study involves Reagent and Phosphoric acid, a branch of Organic chemistry. His Stereocenter, Nucleophile and Stereoselectivity study, which is part of a larger body of work in Catalysis, is frequently linked to Structural diversity and Substrate, bridging the gap between disciplines.
His Nucleophile research is multidisciplinary, incorporating elements of Oxindole and Phosphine. Bin Tan combines subjects such as In situ, Primary, Trichloroisocyanuric acid, Brønsted–Lowry acid–base theory and Bond formation with his study of Enantioselective synthesis. His Combinatorial chemistry research is multidisciplinary, incorporating perspectives in Optically active, Michael reaction and Nitroalkane.
Bin Tan mostly deals with Catalysis, Organic chemistry, Enantioselective synthesis, Combinatorial chemistry and Organocatalysis. His Catalysis study combines topics in areas such as Stereochemistry and Phosphoric acid. His Organic chemistry study focuses mostly on Stereocenter, Michael reaction, Stereoselectivity, Nucleophile and Cycloaddition.
His work in Michael reaction addresses subjects such as Intramolecular force, which are connected to disciplines such as Trifluoromethyl. Bin Tan has researched Enantioselective synthesis in several fields, including Bifunctional, Iminium, Cascade reaction and Brønsted–Lowry acid–base theory. In his research, Quinone is intimately related to Chirality, which falls under the overarching field of Combinatorial chemistry.
Bin Tan mainly focuses on Combinatorial chemistry, Enantioselective synthesis, Catalysis, Axial symmetry and Atropisomer. His work carried out in the field of Combinatorial chemistry brings together such families of science as Reaction conditions and Molecule. His research in Enantioselective synthesis intersects with topics in Bifunctional, Electrophile and Ligand.
His research integrates issues of Cascade reaction, Stereocenter and Ring in his study of Bifunctional. Bin Tan interconnects Aryl, Phosphoric acid and Density functional theory in the investigation of issues within Catalysis. The various areas that he examines in his Atropisomer study include Axial chirality, Organocatalysis and Chirality.
Combinatorial chemistry, Enantioselective synthesis, Catalysis, Atropisomer and Axial symmetry are his primary areas of study. His Combinatorial chemistry research incorporates elements of Electrophile, Chirality and Phosphoric acid. His work on NOBIN and Desymmetrization as part of general Enantioselective synthesis research is frequently linked to Rational design, bridging the gap between disciplines.
His NOBIN study integrates concerns from other disciplines, such as Oxazoline, Redox and Ligand. His work deals with themes such as Reaction conditions, Kinetic resolution and Optically active, which intersect with Desymmetrization. His Regioselectivity research includes elements of Axial chirality, Steric effects and Quinone.
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Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies
Daojuan Cheng;Yoshihiro Ishihara;Bin Tan;Bin Tan;Carlos F. Barbas.
ACS Catalysis (2014)
Construction of bispirooxindoles containing three quaternary stereocentres in a cascade using a single multifunctional organocatalyst
Bin Tan;Nuno R. Candeias;Nuno R. Candeias;Carlos F. Barbas.
Nature Chemistry (2011)
Core-Structure-Motivated Design of a Phosphine-Catalyzed [3 + 2] Cycloaddition Reaction: Enantioselective Syntheses of Spirocyclopenteneoxindoles
Bin Tan;Nuno R. Candeias;Nuno R. Candeias;Carlos F. Barbas.
Journal of the American Chemical Society (2011)
Construction of Axially Chiral Compounds via Asymmetric Organocatalysis
Yong-Bin Wang;Bin Tan.
Accounts of Chemical Research (2018)
Highly Efficient Hydrogen-Bonding Catalysis of the Diels–Alder Reaction of 3-Vinylindoles and Methyleneindolinones Provides Carbazolespirooxindole Skeletons
Bin Tan;Gloria Hernández-Torres;Gloria Hernández-Torres;Carlos F Barbas.
Journal of the American Chemical Society (2011)
Atroposelective Synthesis of Axially Chiral Biaryldiols via Organocatalytic Arylation of 2-Naphthols.
Ye-Hui Chen;Dao-Juan Cheng;Jian Zhang;Yong Wang.
Journal of the American Chemical Society (2015)
A Dual-Catalytic Strategy To Direct Asymmetric Radical Aminotrifluoromethylation of Alkenes
Jin-Shun Lin;Xiao-Yang Dong;Tao-Tao Li;Na-Chuan Jiang.
Journal of the American Chemical Society (2016)
Organocatalytic asymmetric arylation of indoles enabled by azo groups
Liang-Wen Qi;Jian-Hui Mao;Jian Zhang;Bin Tan.
Nature Chemistry (2018)
Enantioselective C-H bond functionalization triggered by radical trifluoromethylation of unactivated alkene.
Peng Yu;Jin-Shun Lin;Lei Li;Sheng-Cai Zheng.
Angewandte Chemie (2014)
Highly Atroposelective Synthesis of Arylpyrroles by Catalytic Asymmetric Paal–Knorr Reaction
Lei Zhang;Jian Zhang;Ji Ma;Dao-Juan Cheng.
Journal of the American Chemical Society (2017)
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