What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Enzyme
The scientist’s investigation covers issues in Organic chemistry, Stereochemistry, Medicinal chemistry, Photochemistry and Catalysis.
His work is connected to Hydrolysis, Enzyme catalyzed, Aliphatic compound, Enantiomeric excess and Stereoselectivity, as a part of Organic chemistry.
His Hydrolysis study combines topics from a wide range of disciplines, such as Ketone, Racemization, Acid catalysis and Enantioselective synthesis.
His work deals with themes such as Amino acid, Amide, Hydroxynitrile lyase, Enzyme and Cyanohydrin, which intersect with Stereochemistry.
His study in Medicinal chemistry is interdisciplinary in nature, drawing from both Molecular wire, Aryl, Sequence and Nucleophile.
Franz Effenberger has included themes like Solvatochromism, Radical ion, Polarography, Intramolecular force and Absorption spectroscopy in his Photochemistry study.
His most cited work include:
- Low-voltage organic transistors with an amorphous molecular gate dielectric (703 citations)
- Synthesis and Reactions of Optically Active Cyanohydrins (251 citations)
- Anion-exchange membranes with improved alkaline stability (191 citations)
What are the main themes of his work throughout his whole career to date?
Franz Effenberger spends much of his time researching Medicinal chemistry, Organic chemistry, Stereochemistry, Catalysis and Polymer chemistry.
His research integrates issues of Steric effects, Aliphatic compound, Alkyl and Amide in his study of Medicinal chemistry.
His research related to Acylation, Hydrolysis, Yield, Aryl and Enzyme catalyzed might be considered part of Organic chemistry.
His Stereochemistry research incorporates elements of Amino acid, Hydroxynitrile lyase, Enzyme, Cyanohydrin and Stereoselectivity.
He most often published in these fields:
- Medicinal chemistry (32.38%)
- Organic chemistry (30.69%)
- Stereochemistry (24.28%)
What were the highlights of his more recent work (between 1997-2017)?
- Organic chemistry (30.69%)
- Stereochemistry (24.28%)
- Hydroxynitrile lyase (5.40%)
In recent papers he was focusing on the following fields of study:
Organic chemistry, Stereochemistry, Hydroxynitrile lyase, Stereoselectivity and Catalysis are his primary areas of study.
Organic chemistry is closely attributed to Polymer chemistry in his work.
His Stereochemistry research is multidisciplinary, incorporating perspectives in Lyase, Substrate, Enzyme, Hydrolysis and Cyanohydrin.
The study incorporates disciplines such as Yield, Sulfanyl, Medicinal chemistry, Racemization and Enantiomer in addition to Stereoselectivity.
His Medicinal chemistry research includes themes of Ketone and Acylation.
His work carried out in the field of Catalysis brings together such families of science as Steric effects, Alkyl and Tautomer.
Between 1997 and 2017, his most popular works were:
- Low-voltage organic transistors with an amorphous molecular gate dielectric (703 citations)
- Photoactivated Preparation and Patterning of Self-Assembled Monolayers with 1-Alkenes and Aldehydes on Silicon Hydride Surfaces. (170 citations)
- Influence of Aromatic Groups Incorporated in Long-Chain Alkanethiol Self-Assembled Monolayers on Gold (106 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Enzyme
His primary areas of study are Stereochemistry, Hydroxynitrile lyase, Organic chemistry, Enzyme and Hydrolysis.
His Stereochemistry research is multidisciplinary, incorporating elements of Thiophene, Graphite and Scanning tunneling microscope.
His work in Hydroxynitrile lyase addresses issues such as Active site, which are connected to fields such as Substrate, Lyase, Cyanohydrin and Stereospecificity.
His study in Stereoselectivity, Catalysis, Solvent, Protecting group and Bromine falls under the purview of Organic chemistry.
His research integrates issues of Racemization, Nitrile, Nitrile hydratase and Amide in his study of Hydrolysis.
His Nitrilase research integrates issues from Yield and Regioselectivity.
This overview was generated by a machine learning system which analysed the scientist’s
body of work. If you have any feedback, you can
contact us
here.
