What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
His primary scientific interests are in Organic chemistry, Catalysis, Enantioselective synthesis, Stereochemistry and Organocatalysis.
His study in Organic chemistry focuses on Amine gas treating, Bifunctional, Cycloaddition, Electrophile and Tsuji–Trost reaction.
His Catalysis research focuses on Stereoselectivity in particular.
His Enantioselective synthesis research is multidisciplinary, incorporating perspectives in Phosphorus, Primary, Lewis acids and bases, Michael reaction and Methylene.
His Stereochemistry research includes themes of Brønsted–Lowry acid–base theory, Stereocenter and Stereoisomerism.
His Stereoisomerism research incorporates elements of Alkylation and Annulation.
His most cited work include:
- Trienamines in asymmetric organocatalysis: Diels-Alder and tandem reactions. (276 citations)
- Highly Asymmetric Michael Addition to α,β‐Unsaturated Ketones Catalyzed by 9‐Amino‐9‐deoxyepiquinine (250 citations)
- Organocatalytic asymmetric transformations of modified Morita–Baylis–Hillman adducts (227 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Catalysis, Organic chemistry, Enantioselective synthesis, Amine gas treating and Organocatalysis.
His Catalysis study integrates concerns from other disciplines, such as Combinatorial chemistry, Stereochemistry and Medicinal chemistry.
He studied Combinatorial chemistry and Allylic rearrangement that intersect with Alkylation.
He has researched Stereochemistry in several fields, including Stereocenter, Molecule, Stereoisomerism, Annulation and Domino.
His Enantioselective synthesis research incorporates themes from Aryl, Electrophile, Primary and Addition reaction.
Ying-Chun Chen interconnects Iminium, Bicyclic molecule and Carbene in the investigation of issues within Amine gas treating.
He most often published in these fields:
- Catalysis (95.80%)
- Organic chemistry (63.59%)
- Enantioselective synthesis (36.69%)
What were the highlights of his more recent work (between 2017-2021)?
- Catalysis (95.80%)
- Medicinal chemistry (23.53%)
- Combinatorial chemistry (23.25%)
In recent papers he was focusing on the following fields of study:
Ying-Chun Chen mainly focuses on Catalysis, Medicinal chemistry, Combinatorial chemistry, Annulation and Cycloaddition.
His Catalysis study is related to the wider topic of Organic chemistry.
His study focuses on the intersection of Combinatorial chemistry and fields such as Lewis acids and bases with connections in the field of Electrophile, Tsuji–Trost reaction and Double bond.
His Annulation study incorporates themes from Sulfonium, Brønsted–Lowry acid–base theory, Oxindole and DABCO.
His studies in Cycloaddition integrate themes in fields like Iminium and Chemoselectivity.
His research integrates issues of Tertiary amine, Organocatalysis, Stereochemistry and Michael reaction in his study of Stereoselectivity.
Between 2017 and 2021, his most popular works were:
- Plasma asprosin concentrations are increased in individuals with glucose dysregulation and correlated with insulin resistance and first-phase insulin secretion (41 citations)
- Asymmetric Barton–Zard Reaction To Access 3-Pyrrole-Containing Axially Chiral Skeletons (36 citations)
- Asymmetric Barton–Zard Reaction To Access 3-Pyrrole-Containing Axially Chiral Skeletons (36 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Ying-Chun Chen spends much of his time researching Catalysis, Combinatorial chemistry, Stereoselectivity, Annulation and Medicinal chemistry.
His work on Cycloaddition, Enantioselective synthesis, Bifunctional and Phosphine as part of general Catalysis research is often related to Rotation, thus linking different fields of science.
His Enantioselective synthesis research is under the purview of Organic chemistry.
His work carried out in the field of Combinatorial chemistry brings together such families of science as Allylic rearrangement and Lewis acids and bases.
His study looks at the intersection of Stereoselectivity and topics like Organocatalysis with Chemoselectivity, Enone, Steric effects and Cinchona.
His work deals with themes such as Tertiary amine and Stereochemistry, which intersect with Annulation.
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