What is she best known for?
The fields of study she is best known for:
- Organic chemistry
- Catalysis
- Aldehyde
Géraldine Masson mainly investigates Organic chemistry, Catalysis, Enantioselective synthesis, Phosphoric acid and Brønsted–Lowry acid–base theory.
Her work on Cycloaddition, Ugi reaction, Isocyanide and Aldehyde as part of general Organic chemistry study is frequently connected to Visible spectrum, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
Géraldine Masson has researched Catalysis in several fields, including Organic molecules and Intermolecular force.
Her Enantioselective synthesis research includes themes of Adduct, Baylis–Hillman reaction, Stereochemistry and Lewis acids and bases.
In her study, Stereoisomerism, Halogenation, Salt and Calcium is inextricably linked to Enantiomer, which falls within the broad field of Phosphoric acid.
In her study, Stereocenter and Diels–Alder reaction is strongly linked to Povarov reaction, which falls under the umbrella field of Brønsted–Lowry acid–base theory.
Her most cited work include:
- The Enantioselective Morita–Baylis–Hillman Reaction and Its Aza Counterpart (377 citations)
- Chiral Brønsted Acid-Catalyzed Enantioselective Three-Component Povarov Reaction (258 citations)
- Catalytic enantioselective [4 + 2]-cycloaddition: a strategy to access aza-hexacycles (181 citations)
What are the main themes of her work throughout her whole career to date?
Géraldine Masson spends much of her time researching Catalysis, Organic chemistry, Enantioselective synthesis, Combinatorial chemistry and Phosphoric acid.
Her Catalysis research integrates issues from Iodine and Stereochemistry.
As a part of the same scientific family, Géraldine Masson mostly works in the field of Stereochemistry, focusing on Baylis–Hillman reaction and, on occasion, Bifunctional.
Her work on Cycloaddition, Diels–Alder reaction, Yield and Aldehyde as part of general Organic chemistry research is frequently linked to Oxidative phosphorylation, bridging the gap between disciplines.
Her Enantioselective synthesis study focuses on Organocatalysis in particular.
The various areas that Géraldine Masson examines in her Combinatorial chemistry study include Reactivity, Molecule, Organic synthesis and Double bond.
She most often published in these fields:
- Catalysis (51.35%)
- Organic chemistry (50.81%)
- Enantioselective synthesis (42.70%)
What were the highlights of her more recent work (between 2016-2021)?
- Catalysis (51.35%)
- Enantioselective synthesis (42.70%)
- Combinatorial chemistry (27.03%)
In recent papers she was focusing on the following fields of study:
The scientist’s investigation covers issues in Catalysis, Enantioselective synthesis, Combinatorial chemistry, Organic chemistry and Cycloaddition.
The concepts of her Catalysis study are interwoven with issues in Iodine and Tetrazine.
Géraldine Masson is interested in Organocatalysis, which is a field of Enantioselective synthesis.
Géraldine Masson interconnects Brønsted–Lowry acid–base theory, Photoredox catalysis and Stereoselectivity in the investigation of issues within Organocatalysis.
In her work, Catalytic oxidation, Synthon and Ring is strongly intertwined with Molecule, which is a subfield of Combinatorial chemistry.
Her work carried out in the field of Cycloaddition brings together such families of science as Reaction conditions and Hydrogen bond.
Between 2016 and 2021, her most popular works were:
- Enantioselective Brønsted Acid Catalysis as a Tool for the Synthesis of Natural Products and Pharmaceuticals (49 citations)
- Fluorinated Sulfilimino Iminiums: Efficient and Versatile Sources of Perfluoroalkyl Radicals under Photoredox Catalysis (37 citations)
- Enantioselective Organocatalytic Intramolecular Aza‐Diels–Alder Reaction (22 citations)
In her most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Aldehyde
Géraldine Masson focuses on Enantioselective synthesis, Catalysis, Combinatorial chemistry, Cycloaddition and Iodine.
Her Catalysis study introduces a deeper knowledge of Organic chemistry.
Her research investigates the connection between Combinatorial chemistry and topics such as Organocatalysis that intersect with problems in Retrosynthetic analysis and Brønsted–Lowry acid–base theory.
Her research integrates issues of Protecting group, Diels–Alder reaction, Phosphoric acid, Hydrogen bond and Redox in her study of Cycloaddition.
Her Phosphoric acid research includes elements of Phosphate, Stereocenter and Lewis acids and bases.
Her biological study spans a wide range of topics, including Stoichiometry, Stereoselectivity, Planar chirality and Sulfonyl.
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