What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Enzyme
Dennis G. Hall mainly investigates Organic chemistry, Catalysis, Enantioselective synthesis, Allylic rearrangement and Lewis acids and bases.
His work is connected to Boronic acid, Boron, Suzuki reaction, Borylation and Organic synthesis, as a part of Organic chemistry.
His Boronic acid study necessitates a more in-depth grasp of Combinatorial chemistry.
His Catalysis study integrates concerns from other disciplines, such as Yield, Reagent, Reactivity and Stereochemistry.
His Enantioselective synthesis study combines topics in areas such as Stereoisomerism, Brønsted–Lowry acid–base theory, Diol, Pinacol and Stereoselectivity.
Dennis G. Hall works mostly in the field of Allylic rearrangement, limiting it down to topics relating to Imine and, in certain cases, Silicon and Nucleophile, as a part of the same area of interest.
His most cited work include:
- Natural product synthesis using multicomponent reaction strategies. (1118 citations)
- Boronic acids : preparation and applications in organic synthesis and medicine (657 citations)
- Boronic acids : preparation and applications in organic synthesis, medicine and materials (520 citations)
What are the main themes of his work throughout his whole career to date?
Dennis G. Hall mainly focuses on Organic chemistry, Catalysis, Enantioselective synthesis, Combinatorial chemistry and Stereochemistry.
His works in Boronic acid, Allylic rearrangement, Reagent, Stereoselectivity and Cycloaddition are all subjects of inquiry into Organic chemistry.
His Allylic rearrangement research includes elements of Borylation and Organic synthesis.
The study incorporates disciplines such as Yield and Substrate in addition to Catalysis.
His work deals with themes such as Aldehyde, Enol, Diol, Aryl and Pinacol, which intersect with Enantioselective synthesis.
His Stereochemistry research integrates issues from Diels alder and Ring.
He most often published in these fields:
- Organic chemistry (45.72%)
- Catalysis (33.09%)
- Enantioselective synthesis (25.28%)
What were the highlights of his more recent work (between 2015-2021)?
- Combinatorial chemistry (23.42%)
- Organic chemistry (45.72%)
- Enantioselective synthesis (25.28%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Combinatorial chemistry, Organic chemistry, Enantioselective synthesis, Boronic acid and Catalysis.
Dennis G. Hall interconnects Diol, Ring and Nucleophile in the investigation of issues within Combinatorial chemistry.
His research on Organic chemistry frequently links to adjacent areas such as Amino acid.
His Enantioselective synthesis research incorporates themes from Aryl, Nonaflate, Borylation and Cyclobutanes.
He has researched Boronic acid in several fields, including Adduct and Electrophile.
His work carried out in the field of Catalysis brings together such families of science as Yield, Halide, Reactivity and Carbocation.
Between 2015 and 2021, his most popular works were:
- Bioinspired Self-Healing Hydrogel Based on Benzoxaborole-Catechol Dynamic Covalent Chemistry for 3D Cell Encapsulation (56 citations)
- Multicomponent Hetero-[4 + 2] Cycloaddition/Allylboration Reaction: From Natural Product Synthesis to Drug Discovery (50 citations)
- Boronic acid catalysis. (45 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Enzyme
Dennis G. Hall spends much of his time researching Combinatorial chemistry, Boronic acid, Bioorthogonal chemistry, Organic chemistry and Click chemistry.
His Combinatorial chemistry research is multidisciplinary, relying on both Covalent bond and Cell encapsulation.
He regularly links together related areas like Catalysis in his Boronic acid studies.
The Catalysis study which covers Carbocation that intersects with Yield, Alkylation, Enantioselective synthesis, Electrophile and Organic reaction.
His Organic chemistry and Allylic rearrangement, Cycloaddition, Amide, Substrate and Enantiomer investigations all form part of his Organic chemistry research activities.
His Allylic rearrangement research incorporates elements of Natural product, Molecule, Drug discovery and Stereoselectivity.
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