What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
Wanbin Zhang spends much of his time researching Catalysis, Organic chemistry, Palladium, Medicinal chemistry and Tsuji–Trost reaction.
His studies deal with areas such as Ligand and Stereochemistry as well as Catalysis.
His research investigates the connection between Palladium and topics such as Pyrrolidine that intersect with issues in Ketone, Organocatalysis and Reagent.
His Medicinal chemistry research includes themes of Steric effects, Dimethyl malonate, Hydrogen bond, Intramolecular force and Reaction mechanism.
His Tsuji–Trost reaction research is multidisciplinary, relying on both Alkylation, Planar chirality, Enantiopure drug and Nucleophile.
His study looks at the relationship between Enantioselective synthesis and topics such as Stereoisomerism, which overlap with Succinimides.
His most cited work include:
- Copper-catalyzed C-H functionalization reactions: efficient synthesis of heterocycles. (519 citations)
- Transition metal-catalyzed allylic substitution reactions with unactivated allylic substrates (198 citations)
- C–N Bond Cleavage of Allylic Amines via Hydrogen Bond Activation with Alcohol Solvents in Pd-Catalyzed Allylic Alkylation of Carbonyl Compounds (167 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Catalysis, Organic chemistry, Medicinal chemistry, Enantioselective synthesis and Combinatorial chemistry.
His Catalysis research incorporates themes from Ligand and Stereochemistry.
Wanbin Zhang interconnects Oxazoline, Planar chirality, Stereocenter and Axial chirality in the investigation of issues within Stereochemistry.
The Medicinal chemistry study combines topics in areas such as Steric effects, Reaction conditions, Aryl, Alkyl and Stereoselectivity.
His Asymmetric hydrogenation study integrates concerns from other disciplines, such as Noyori asymmetric hydrogenation, Rhodium and Iridium.
In general Allylic rearrangement, his work in Tsuji–Trost reaction is often linked to Substitution linking many areas of study.
He most often published in these fields:
- Catalysis (69.53%)
- Organic chemistry (33.33%)
- Medicinal chemistry (27.08%)
What were the highlights of his more recent work (between 2016-2021)?
- Catalysis (69.53%)
- Combinatorial chemistry (23.96%)
- Enantioselective synthesis (25.78%)
In recent papers he was focusing on the following fields of study:
His scientific interests lie mostly in Catalysis, Combinatorial chemistry, Enantioselective synthesis, Asymmetric hydrogenation and Medicinal chemistry.
His work deals with themes such as Ligand and Stereochemistry, which intersect with Catalysis.
His work in Combinatorial chemistry addresses subjects such as Transition metal, which are connected to disciplines such as Reagent.
His Enantioselective synthesis research is multidisciplinary, relying on both Amino acid, Bicyclic molecule, Catalytic cycle and Copper.
As part of the same scientific family, Wanbin Zhang usually focuses on Asymmetric hydrogenation, concentrating on Nickel and intersecting with Sulfonyl and Polymer chemistry.
His biological study spans a wide range of topics, including Rhodium, Reaction conditions, Ring and Regioselectivity.
Between 2016 and 2021, his most popular works were:
- Ir/Cu Dual Catalysis: Enantio- and Diastereodivergent Access to α,α-Disubstituted α-Amino Acids Bearing Vicinal Stereocenters (69 citations)
- Renaissance of pyridine-oxazolines as chiral ligands for asymmetric catalysis (59 citations)
- Stereoselective and Site-Specific Allylic Alkylation of Amino Acids and Small Peptides via a Pd/Cu Dual Catalysis (59 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Wanbin Zhang focuses on Catalysis, Enantioselective synthesis, Combinatorial chemistry, Allylic rearrangement and Organic chemistry.
The various areas that Wanbin Zhang examines in his Catalysis study include Reactivity, Ligand, Medicinal chemistry and Stereochemistry.
His research integrates issues of Alkylation and Tsuji–Trost reaction in his study of Stereochemistry.
His studies deal with areas such as Brønsted–Lowry acid–base theory, Catalytic cycle, Molecule and Lewis acids and bases as well as Enantioselective synthesis.
His Combinatorial chemistry research includes themes of Oxygen, Organic synthesis and Intermolecular force.
His Allylic rearrangement research also works with subjects such as
- Amination which intersects with area such as Alcohol and Amino esters,
- Chiral ligand and related Enantiopure drug.
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