What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
His scientific interests lie mostly in Organic chemistry, Stereochemistry, Medicinal chemistry, Aliphatic compound and Bicyclic molecule.
His work blends Organic chemistry and Beta studies together.
His Stereochemistry research integrates issues from Protonation, Carboxylic acid, Cyclopentadienyl complex and Active site.
The Medicinal chemistry study combines topics in areas such as Ion, Heptane and Crystal structure.
His Aliphatic compound study integrates concerns from other disciplines, such as Acetal, Diels–Alder reaction, Aldehyde, Hydrocarbon and Ketone.
His studies in Bicyclic molecule integrate themes in fields like Fluorocarbon, Metal, Haloketone and Addition reaction.
His most cited work include:
- An explanation for rapid enzyme-catalyzed proton abstraction from carbon acids: importance of late transition states in concerted mechanisms (243 citations)
- Understanding enzyme-catalyzed proton abstraction from carbon acids: Details of stepwise mechanisms for β-elimination reactions (147 citations)
- A general procedure for the base-promoted hydrolysis of hindered esters at ambient temperatures (125 citations)
What are the main themes of his work throughout his whole career to date?
Paul G. Gassman mainly focuses on Medicinal chemistry, Organic chemistry, Bicyclic molecule, Stereochemistry and Photochemistry.
His Medicinal chemistry research is multidisciplinary, incorporating elements of Heptane, Moiety, Ring, Solvolysis and Ion.
Diels–Alder reaction, Ionic bonding, Aliphatic compound, Diels alder and Alkylation are the primary areas of interest in his Organic chemistry study.
His research in Diels–Alder reaction intersects with topics in Intramolecular force and Cycloaddition.
His study on Bicyclic molecule also encompasses disciplines like
- Bent molecular geometry together with Crystallography and Sigma bond,
- Transition metal which is related to area like Polymer chemistry.
Paul G. Gassman merges many fields, such as Stereochemistry and Diene, in his writings.
He most often published in these fields:
- Medicinal chemistry (37.16%)
- Organic chemistry (27.87%)
- Bicyclic molecule (20.77%)
What were the highlights of his more recent work (between 1989-2007)?
- Medicinal chemistry (37.16%)
- Organic chemistry (27.87%)
- Stereochemistry (17.21%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Medicinal chemistry, Organic chemistry, Stereochemistry, Diels–Alder reaction and Bicyclic molecule.
His Medicinal chemistry research incorporates elements of Aliphatic compound, Molecule, Trifluoromethyl and Cyclopentadienyl complex.
His research ties Electrochemistry and Organic chemistry together.
His work on Electronic effect as part of general Stereochemistry research is frequently linked to Skeleton, bridging the gap between disciplines.
His Diels–Alder reaction study integrates concerns from other disciplines, such as Ionic bonding, Intramolecular force and Cycloaddition.
His Bicyclic molecule study combines topics from a wide range of disciplines, such as Solvolysis, Fluorocarbon, Haloketone and Addition reaction.
Between 1989 and 2007, his most popular works were:
- An explanation for rapid enzyme-catalyzed proton abstraction from carbon acids: importance of late transition states in concerted mechanisms (243 citations)
- Understanding enzyme-catalyzed proton abstraction from carbon acids: Details of stepwise mechanisms for β-elimination reactions (147 citations)
- Electrophilic catalysis can explain the unexpected acidity of carbon acids in enzyme-catalyzed reactions (115 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Organic chemistry, Medicinal chemistry, Bicyclic molecule, Diels–Alder reaction and Stereochemistry are his primary areas of study.
Paul G. Gassman combines Organic chemistry and Mandelate racemase in his studies.
He mostly deals with Substituent in his studies of Medicinal chemistry.
His biological study spans a wide range of topics, including Solvolysis, Fluorocarbon, Haloketone and Addition reaction.
His Diels–Alder reaction study also includes
- Cycloaddition which is related to area like Scientific method, Cyclobutane and Carbocation,
- Intramolecular reaction which intersects with area such as Aliphatic compound, Hydrocarbon and Acid catalysis.
His Stereochemistry research is multidisciplinary, incorporating elements of Crystallography, Protonation, Carboxylic acid and Active site.
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