What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Enzyme
His primary areas of investigation include Organic chemistry, Catalysis, Combinatorial chemistry, Nickel and Aryne.
His Organic chemistry research is mostly focused on the topic Aryl.
His research in Catalysis focuses on subjects like Amide, which are connected to Synthon and Nucleophile.
His research ties Natural product and Combinatorial chemistry together.
His Nickel study combines topics in areas such as Carbon, Oxygen and Palladium.
The concepts of his Aryne study are interwoven with issues in Computational chemistry, Molecule and Regioselectivity.
His most cited work include:
- Nickel-Catalyzed Cross-Couplings Involving Carbon-Oxygen Bonds (824 citations)
- Cross-coupling reactions of aryl pivalates with boronic acids. (274 citations)
- Conversion of amides to esters by the nickel-catalysed activation of amide C-N bonds (238 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Organic chemistry, Combinatorial chemistry, Catalysis, Stereochemistry and Total synthesis.
All of his Organic chemistry and Molecule, Phenol and Reagent investigations are sub-components of the entire Organic chemistry study.
His Combinatorial chemistry research includes elements of Ketone, Aryne, Electrophile and Ring.
His Catalysis research includes themes of Aryl, Nickel and Amide.
The various areas that Neil K. Garg examines in his Stereochemistry study include Chemical synthesis, Stereocenter, Isothiocyanate and Stereoisomerism.
His research in Total synthesis intersects with topics in Natural product and Bicyclic molecule.
He most often published in these fields:
- Organic chemistry (33.83%)
- Combinatorial chemistry (27.36%)
- Catalysis (27.36%)
What were the highlights of his more recent work (between 2017-2021)?
- Combinatorial chemistry (27.36%)
- Catalysis (27.36%)
- Stereochemistry (24.38%)
In recent papers he was focusing on the following fields of study:
Neil K. Garg mostly deals with Combinatorial chemistry, Catalysis, Stereochemistry, Stereocenter and Organic chemistry.
His Combinatorial chemistry research incorporates themes from Substrate, Ketone, Chemical synthesis, Trifluoromethanesulfonate and Silylation.
His Catalysis research integrates issues from Computational chemistry, Glovebox, Nickel and Amide.
His research in the fields of Total synthesis overlaps with other disciplines such as Nucleobase.
His study in Total synthesis is interdisciplinary in nature, drawing from both Molecule and Alkaloid.
In the subject of general Organic chemistry, his work in 8-Hydroxygeraniol and McFadyen–Stevens reaction is often linked to Student engagement, Chemistry education and Reputation, thereby combining diverse domains of study.
Between 2017 and 2021, his most popular works were:
- Nickel-Catalyzed Suzuki-Miyaura Coupling of Aliphatic Amides. (35 citations)
- Diels–Alder cycloadditions of strained azacyclic allenes (22 citations)
- Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki-Miyaura and Negishi Cross-Coupling Reactions for Tetra-ortho-Substituted Biaryl Synthesis. (18 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Enzyme
His primary areas of study are Combinatorial chemistry, Catalysis, Stereocenter, Stereochemistry and Stereoselectivity.
His Combinatorial chemistry research is multidisciplinary, incorporating elements of Aryne, Negishi coupling, Catalytic cycle, Substrate and Nucleophile.
His studies in Substrate integrate themes in fields like Electrophile, Nickel, Sequence, Amide and Ketone.
His research on Catalysis often connects related areas such as Polymer chemistry.
His study looks at the relationship between Stereocenter and topics such as Chemical synthesis, which overlap with Diels alder, Ring, Aqueous medium and Enzyme binding.
Stereochemistry is closely attributed to Stereoisomerism in his research.
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