What is he best known for?
The fields of study he is best known for:
- Enzyme
- Organic chemistry
- Catalysis
Wolfgang Kroutil mostly deals with Organic chemistry, Biocatalysis, Stereochemistry, Enantioselective synthesis and Substrate.
His study in Organic chemistry focuses on Alcohol dehydrogenase, Enantiomer, Kinetic resolution, Redox and Stereoisomerism.
His studies deal with areas such as Combinatorial chemistry and Organic synthesis as well as Biocatalysis.
His Stereochemistry study integrates concerns from other disciplines, such as Vicinal, Aldehyde, Enzyme, Hydrolysis and Stereoselectivity.
His Enantioselective synthesis research incorporates themes from Reductive amination and Transamination.
Wolfgang Kroutil works mostly in the field of Substrate, limiting it down to topics relating to Reductase and, in certain cases, Chemoselectivity, Nitroalkene, Active site and Conjugated system, as a part of the same area of interest.
His most cited work include:
- Recent advances in the biocatalytic reduction of ketones and oxidation of sec-alcohols. (330 citations)
- ω-Transaminases for the synthesis of non-racemic α-chiral primary amines (329 citations)
- Artificial Biocatalytic Linear Cascades for Preparation of Organic Molecules (231 citations)
What are the main themes of his work throughout his whole career to date?
The scientist’s investigation covers issues in Organic chemistry, Stereochemistry, Biocatalysis, Catalysis and Enantioselective synthesis.
His research in Stereoselectivity, Yield, Enantiomer, Ketone and Kinetic resolution are components of Organic chemistry.
His research investigates the connection with Stereochemistry and areas like Enzyme which intersect with concerns in Cleavage.
In his study, Redox is inextricably linked to Combinatorial chemistry, which falls within the broad field of Biocatalysis.
His research investigates the link between Catalysis and topics such as Alcohol dehydrogenase that cross with problems in Acetone.
His Enantioselective synthesis study which covers Amination that intersects with Amine gas treating.
He most often published in these fields:
- Organic chemistry (47.75%)
- Stereochemistry (32.15%)
- Biocatalysis (27.90%)
What were the highlights of his more recent work (between 2017-2021)?
- Biocatalysis (27.90%)
- Stereochemistry (32.15%)
- Combinatorial chemistry (14.89%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include Biocatalysis, Stereochemistry, Combinatorial chemistry, Catalysis and Organic chemistry.
His Biocatalysis research is multidisciplinary, incorporating perspectives in Kinetic resolution, Enantioselective synthesis, Pictet–Spengler reaction, Biotransformation and Protein engineering.
His Stereochemistry research is multidisciplinary, incorporating elements of Regioselectivity, Active site, Substrate, Pseudomonas protegens and Amine gas treating.
His studies in Combinatorial chemistry integrate themes in fields like Amination, Photocatalysis, Enantiomeric excess, Cofactor and Stereoselectivity.
His work on Reaction intermediate as part of general Catalysis study is frequently linked to Context, therefore connecting diverse disciplines of science.
His study in Organic chemistry concentrates on Carbon–nitrogen bond and Trifluoromethylation.
Between 2017 and 2021, his most popular works were:
- Artificial Biocatalytic Linear Cascades for Preparation of Organic Molecules (231 citations)
- Photo-Biocatalysis: Biotransformations in the Presence of Light (68 citations)
- Mechanistic Studies of Fatty Acid Activation by CYP152 Peroxygenases Reveal Unexpected Desaturase Activity (33 citations)
In his most recent research, the most cited papers focused on:
- Enzyme
- Organic chemistry
- Catalysis
His scientific interests lie mostly in Biocatalysis, Combinatorial chemistry, Stereochemistry, Amination and Enantioselective synthesis.
His Biocatalysis study incorporates themes from Oxidation reduction, Cascade and Biotransformation, Enzyme.
His Combinatorial chemistry study combines topics in areas such as Chemical reaction, Methylation, Enantiomeric excess, Cofactor and Catalysis.
The Stereochemistry study combines topics in areas such as Acyl transferase, Reaction mechanism, Decarboxylation and Hydroxylation.
His research in Amination intersects with topics in Alcohol, Ketone and Turnover number.
The concepts of his Enantioselective synthesis study are interwoven with issues in Alkylation and Stereoselectivity.
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