What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
His primary areas of investigation include Carbene, Organic chemistry, Medicinal chemistry, Stereochemistry and Photochemistry.
His research in Carbene intersects with topics in Electrophile, Ligand, Nucleophile and Alkyl.
His Medicinal chemistry research incorporates themes from Adduct, Allene, Lewis acids and bases and Boron.
His Stereochemistry study integrates concerns from other disciplines, such as Crystallography, Molecule, Ring and Deprotonation.
The Photochemistry study combines topics in areas such as Singlet state, Ammonia and Nitrogen.
His biological study deals with issues like Polymer chemistry, which deal with fields such as Radical ion.
His most cited work include:
- Stable Cyclic Carbenes and Related Species beyond Diaminocarbenes (730 citations)
- Stable Cyclic (Alkyl)(Amino)Carbenes as Rigid or Flexible, Bulky, Electron-Rich Ligands for Transition-Metal Catalysts: A Quaternary Carbon Atom Makes the Difference (614 citations)
- Facile splitting of hydrogen and ammonia by nucleophilic activation at a single carbon center (590 citations)
What are the main themes of his work throughout his whole career to date?
Guy Bertrand mainly focuses on Medicinal chemistry, Carbene, Organic chemistry, Stereochemistry and Photochemistry.
His Medicinal chemistry study combines topics in areas such as Adduct, Reactivity and Electrophile.
His work carried out in the field of Carbene brings together such families of science as Steric effects, Ligand and Alkyl.
In his study, Polymerization and Metal is inextricably linked to Polymer chemistry, which falls within the broad field of Organic chemistry.
In Stereochemistry, he works on issues like Molecule, which are connected to Crystal structure.
His Photochemistry research incorporates elements of Radical and Singlet state.
He most often published in these fields:
- Medicinal chemistry (34.89%)
- Carbene (33.28%)
- Organic chemistry (31.99%)
What were the highlights of his more recent work (between 2013-2021)?
- Carbene (33.28%)
- Alkyl (11.15%)
- Medicinal chemistry (34.89%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Carbene, Alkyl, Medicinal chemistry, Catalysis and Organic chemistry.
The concepts of his Carbene study are interwoven with issues in Ligand, Cationic polymerization, Polymer chemistry and Mesoionic.
His studies in Alkyl integrate themes in fields like Iminium, Substituent, Stereochemistry, Radical and Nucleophile.
The study incorporates disciplines such as Electrophile, Cycloaddition, Lewis acids and bases, Photochemistry and Aryl in addition to Medicinal chemistry.
His Photochemistry study incorporates themes from Coupling reaction, Adduct, Reactivity, Singlet state and Allene.
His Catalysis study combines topics from a wide range of disciplines, such as Combinatorial chemistry and Chloride.
Between 2013 and 2021, his most popular works were:
- Cyclic (Alkyl)(Amino)Carbenes (CAACs): Stable Carbenes on the Rise (409 citations)
- Cyclic (Alkyl)(amino)carbenes (CAACs): Recent Developments (265 citations)
- Synthesis and Reactivity of a CAAC–Aminoborylene Adduct: A Hetero‐Allene or an Organoboron Isoelectronic with Singlet Carbenes (151 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Carbene, Alkyl, Medicinal chemistry, Photochemistry and Organic chemistry are his primary areas of study.
Guy Bertrand combines topics linked to Inorganic chemistry with his work on Carbene.
The various areas that Guy Bertrand examines in his Alkyl study include Cationic polymerization, Radical and Substituent, Stereochemistry.
His biological study spans a wide range of topics, including Cobalt and Homogeneous catalysis.
In his research on the topic of Medicinal chemistry, Transition metal carbene complex, Lone pair and Nucleophile is strongly related with Electrophile.
His Photochemistry research integrates issues from Trimethylsilyl, Cycloaddition, Steric effects, Adduct and Singlet state.
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