What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
The scientist’s investigation covers issues in Hydroamination, Catalysis, Organic chemistry, Medicinal chemistry and Enantioselective synthesis.
His research on Hydroamination concerns the broader Intramolecular force.
His studies link Stereochemistry with Catalysis.
His Stereochemistry research includes elements of Salt, Main group element, Polymer chemistry and Base.
His Organic chemistry study is mostly concerned with Intermolecular force, Amination, Transition metal and Alkyl.
His Medicinal chemistry study combines topics in areas such as Ligand and Metal catalyst.
His most cited work include:
- Hydroamination: direct addition of amines to alkenes and alkynes. (1330 citations)
- Transition Metal‐Catalyzed Asymmetric Hydroamination of Alkenes (AHA) (386 citations)
- 3,3‘-Bis(trisarylsilyl)-Substituted Binaphtholate Rare Earth Metal Catalysts for Asymmetric Hydroamination (258 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Hydroamination, Catalysis, Medicinal chemistry, Organic chemistry and Stereochemistry.
His research integrates issues of Kinetic resolution, Amine gas treating and Intermolecular force in his study of Hydroamination.
Particularly relevant to Enantioselective synthesis is his body of work in Catalysis.
The study incorporates disciplines such as Silylation, Ligand, Alkyl and Metal in addition to Medicinal chemistry.
His Ligand research includes themes of Ring-closing metathesis and Cyclopentadienyl complex.
His studies in Stereochemistry integrate themes in fields like Crystallography, Polymerization, Lanthanum and Reaction mechanism.
He most often published in these fields:
- Hydroamination (55.91%)
- Catalysis (54.84%)
- Medicinal chemistry (41.94%)
What were the highlights of his more recent work (between 2010-2020)?
- Hydroamination (55.91%)
- Catalysis (54.84%)
- Medicinal chemistry (41.94%)
In recent papers he was focusing on the following fields of study:
Kai C. Hultzsch mainly focuses on Hydroamination, Catalysis, Medicinal chemistry, Organic chemistry and Intramolecular force.
His studies deal with areas such as Substituent, Alkene, Ligand and Intermolecular force as well as Hydroamination.
Many of his research projects under Ligand are closely connected to Coordination geometry with Coordination geometry, tying the diverse disciplines of science together.
His Catalysis research is multidisciplinary, incorporating elements of Combinatorial chemistry, Salt metathesis reaction and Polymer chemistry.
His Medicinal chemistry study combines topics from a wide range of disciplines, such as Steric effects, Stereochemistry, Metal and Silylation.
His Intramolecular force study incorporates themes from Enantioselective synthesis and Reaction mechanism.
Between 2010 and 2020, his most popular works were:
- A chiral phenoxyamine magnesium catalyst for the enantioselective hydroamination/cyclization of aminoalkenes and intermolecular hydroamination of vinyl arenes. (108 citations)
- Group 5 Metal Binaphtholate Complexes for Catalytic Asymmetric Hydroaminoalkylation and Hydroamination/Cyclization (85 citations)
- The mechanism of hydroaminoalkylation catalyzed by group 5 metal binaphtholate complexes. (73 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
His primary scientific interests are in Catalysis, Hydroamination, Alkene, Medicinal chemistry and Organic chemistry.
His study in Catalysis is interdisciplinary in nature, drawing from both Benzylamine and Magnesium.
His work deals with themes such as Reaction rate, Amine binding, Polymer chemistry and Amide, which intersect with Alkene.
His Medicinal chemistry research incorporates themes from Isotopic labeling and Steric effects, Moiety, Stereochemistry.
The concepts of his Steric effects study are interwoven with issues in Substituent, Ligand, Lanthanum and Silylation.
His Intramolecular force research is multidisciplinary, relying on both Enantioselective synthesis, Main group element, Transition metal, Alkyne and Allene.
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