What is he best known for?
The fields of study he is best known for:
- Enzyme
- Organic chemistry
- Catalysis
The scientist’s investigation covers issues in Organic chemistry, Stereochemistry, Biocatalysis, Enzyme and Substrate.
His studies deal with areas such as Reductase, Citronellal and Alcohol dehydrogenase as well as Stereochemistry.
The Biocatalysis study combines topics in areas such as Nanotechnology, Biotransformation and Bioconversion.
His Enzyme research includes themes of Stereoisomerism, Acylation, Burkholderia plantarii and Stereoselectivity.
Bernhard Hauer focuses mostly in the field of Substrate, narrowing it down to topics relating to Enantiomer and, in certain cases, Chemoselectivity, Hydrolase, Resolution, Hydrolysis and Gas chromatography.
His Chemical industry research is multidisciplinary, relying on both Amino acid and Optically active.
His most cited work include:
- Industrial biocatalysis today and tomorrow (1809 citations)
- Industrial Methods for the Production of Optically Active Intermediates (1011 citations)
- Asymmetric bioreduction of activated C=C bonds using enoate reductases from the old yellow enzyme family. (265 citations)
What are the main themes of his work throughout his whole career to date?
Bernhard Hauer focuses on Organic chemistry, Stereochemistry, Biochemistry, Enzyme and Biocatalysis.
Catalysis, Scientific method, Benzaldehyde, Enantioselective synthesis and Enantiomer are among the areas of Organic chemistry where the researcher is concentrating his efforts.
Bernhard Hauer works mostly in the field of Benzaldehyde, limiting it down to topics relating to Phenylacetylcarbinol and, in certain cases, Chromatography and Acetaldehyde.
Ene reaction is closely connected to Reductase in his research, which is encompassed under the umbrella topic of Stereochemistry.
His Enzyme research includes elements of Amino acid and Hydrolysis.
His Biocatalysis course of study focuses on Combinatorial chemistry and Protein engineering.
He most often published in these fields:
- Organic chemistry (34.32%)
- Stereochemistry (27.22%)
- Biochemistry (21.89%)
What were the highlights of his more recent work (between 2013-2021)?
- Biocatalysis (19.53%)
- Stereochemistry (27.22%)
- Organic chemistry (34.32%)
In recent papers he was focusing on the following fields of study:
Biocatalysis, Stereochemistry, Organic chemistry, Biochemistry and Enzyme are his primary areas of study.
His Biocatalysis study is focused on Catalysis in general.
His Stereochemistry study combines topics in areas such as Amino acid, Reductase, Hydroxylation, Active site and Stereoselectivity.
His work in the fields of Organic chemistry, such as Enzyme catalysis, Enantioselective synthesis, Biosynthesis and Squalene, overlaps with other areas such as Cover.
His Enzyme study which covers Imine that intersects with Reductive amination.
His Monooxygenase research incorporates elements of Oxidoreductase, Redox and Biotransformation.
Between 2013 and 2021, his most popular works were:
- New Generation of Biocatalysts for Organic Synthesis (214 citations)
- Enzyme toolbox: novel enantiocomplementary imine reductases. (66 citations)
- Directed Evolution Empowered Redesign of Natural Proteins for the Sustainable Production of Chemicals and Pharmaceuticals. (56 citations)
In his most recent research, the most cited papers focused on:
- Enzyme
- Catalysis
- Organic chemistry
His primary areas of study are Biocatalysis, Catalysis, Organic chemistry, Enzyme and Biochemistry.
His Biocatalysis study integrates concerns from other disciplines, such as Monooxygenase, Linoleic acid, Hydroxylation, Enantioselective synthesis and Imine.
His research integrates issues of Combinatorial chemistry, Bioorganic chemistry and Substrate in his study of Catalysis.
His study on Enzyme catalysis and Benzaldehyde is often connected to Chemical synthesis and Epoxide Hydrolases as part of broader study in Organic chemistry.
His work in Enzyme is not limited to one particular discipline; it also encompasses Stereochemistry.
His study in Stereochemistry is interdisciplinary in nature, drawing from both Amino acid, Reductase and Stereoselectivity.
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