What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
Scott D. Rychnovsky mainly focuses on Stereochemistry, Organic chemistry, Prins reaction, Total synthesis and Enantioselective synthesis.
His research links Polyene with Stereochemistry.
His Prins reaction research is multidisciplinary, incorporating elements of Tetrahydropyran, Cope rearrangement, Oxocarbenium, Stereoisomerism and Solvolysis.
His Tetrahydropyran research integrates issues from Regioselectivity and Stereoselectivity.
His research in Total synthesis tackles topics such as Enantiomer which are related to areas like Chain and Triketone.
His Enantioselective synthesis study combines topics from a wide range of disciplines, such as Azide and Imide.
His most cited work include:
- Stereochemistry of alternating polyol chains: 13C NMR analysis of 1,3-diol acetonides (371 citations)
- Analysis of two carbon-13 NMR correlations for determining the stereochemistry of 1,3-diol acetonides (287 citations)
- Oxo Polyene Macrolide Antibiotics (251 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Organic chemistry, Stereochemistry, Combinatorial chemistry, Stereoselectivity and Reagent.
His study in Organic chemistry focuses on Catalysis, Prins reaction, Acetal, Alkylation and Enantioselective synthesis.
The study of Prins reaction is intertwined with the study of Cope rearrangement in a number of ways.
His Stereochemistry study integrates concerns from other disciplines, such as Tetrahydropyran, Ring and Polyene.
Combinatorial chemistry is often connected to Mass spectrometry in his work.
Scott D. Rychnovsky interconnects Alkene, Medicinal chemistry and Synthon in the investigation of issues within Stereoselectivity.
He most often published in these fields:
- Organic chemistry (34.32%)
- Stereochemistry (32.25%)
- Combinatorial chemistry (13.91%)
What were the highlights of his more recent work (between 2011-2021)?
- Combinatorial chemistry (13.91%)
- Organic chemistry (34.32%)
- Stereochemistry (32.25%)
In recent papers he was focusing on the following fields of study:
Scott D. Rychnovsky spends much of his time researching Combinatorial chemistry, Organic chemistry, Stereochemistry, Mass spectrometry and Absolute configuration.
His Combinatorial chemistry research is multidisciplinary, relying on both Coupling reaction, Halide, Aryl and Peptide.
Scott D. Rychnovsky performs multidisciplinary study on Organic chemistry and Acetylation in his works.
Specifically, his work in Stereochemistry is concerned with the study of Intramolecular force.
His study in Mass spectrometry is interdisciplinary in nature, drawing from both Sulfoxide, Computational biology, Cross-Linking Reagents and Protein–protein interaction.
His studies deal with areas such as Kinetic resolution, Catalysis, Enantioselective synthesis, Acylation and 1h nmr spectroscopy as well as Absolute configuration.
Between 2011 and 2021, his most popular works were:
- Hedgehog pathway modulation by multiple lipid binding sites on the smoothened effector of signal response. (137 citations)
- A New in Vivo Cross-linking Mass Spectrometry Platform to Define Protein–Protein Interactions in Living Cells (119 citations)
- Molecular Details Underlying Dynamic Structures and Regulation of the Human 26S Proteasome (55 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Scott D. Rychnovsky mainly investigates Protein–protein interaction, Biochemistry, Organic chemistry, Mass spectrometry and Ring.
The Protein–protein interaction study combines topics in areas such as Amino acid, Plasma protein binding, Lipid metabolism and Proteasome.
The concepts of his Mass spectrometry study are interwoven with issues in Combinatorial chemistry, Computational biology and Cross-Linking Reagents.
His study in Ring is interdisciplinary in nature, drawing from both Alkylation, Total synthesis and Synthon.
Total synthesis is a subfield of Stereochemistry that Scott D. Rychnovsky investigates.
His Stereochemistry research includes elements of Silyl enol ether, Diels alder and Regioselectivity.
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