What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Enzyme
Organic chemistry, Medicinal chemistry, Stereochemistry, Rhodium and Quinone are his primary areas of study.
The concepts of his Organic chemistry study are interwoven with issues in Amino acid and Combinatorial chemistry.
In his study, Copper and Thiazole is strongly linked to Carbene, which falls under the umbrella field of Medicinal chemistry.
The various areas that Christopher J. Moody examines in his Stereochemistry study include Oxidoreductase, Ring, Oxindole and Chemical synthesis.
As a member of one scientific family, he mostly works in the field of Rhodium, focusing on Insertion reaction and, on occasion, Natural product.
His Quinone research incorporates themes from Prodrug, Quinone oxidoreductase and Alkaloid.
His most cited work include:
- Indole synthesis – something old, something new (371 citations)
- From amino acids to heteroaromatics--thiopeptide antibiotics, nature's heterocyclic peptides. (213 citations)
- Oxidative activation of antioxidant defence (206 citations)
What are the main themes of his work throughout his whole career to date?
Christopher J. Moody mainly investigates Organic chemistry, Stereochemistry, Medicinal chemistry, Rhodium and Combinatorial chemistry.
His studies in Diazo, Bicyclic molecule, Enantioselective synthesis, Reagent and Yield are all subfields of Organic chemistry research.
His Stereochemistry research is multidisciplinary, incorporating elements of Ring and Quinone oxidoreductase.
The various areas that Christopher J. Moody examines in his Medicinal chemistry study include Decomposition, Intramolecular force, Cycloaddition and Carbene.
His study with Rhodium involves better knowledge in Catalysis.
His work in Indole test addresses issues such as Oxazole, which are connected to fields such as Natural product and Total synthesis.
He most often published in these fields:
- Organic chemistry (41.94%)
- Stereochemistry (33.81%)
- Medicinal chemistry (26.11%)
What were the highlights of his more recent work (between 2008-2021)?
- Organic chemistry (41.94%)
- Stereochemistry (33.81%)
- Combinatorial chemistry (11.55%)
In recent papers he was focusing on the following fields of study:
Christopher J. Moody mainly focuses on Organic chemistry, Stereochemistry, Combinatorial chemistry, Medicinal chemistry and Catalysis.
His study in Organic chemistry focuses on Diazo, Reagent, Regioselectivity, Naphthoquinone and Yield.
His study in Stereochemistry is interdisciplinary in nature, drawing from both Biochemistry and Chemical synthesis.
His Combinatorial chemistry research includes elements of Amino acid, Intramolecular force, Ring and Drug discovery.
His work in Medicinal chemistry covers topics such as Carbene which are related to areas like Copper.
His research in Catalysis tackles topics such as Oxygen which are related to areas like Photochemistry.
Between 2008 and 2021, his most popular works were:
- Indole synthesis – something old, something new (371 citations)
- Keap calm, and carry on covalently. (106 citations)
- Rhodium carbene routes to oxazoles and thiazoles. Catalyst effects in the synthesis of oxazole and thiazole carboxylates, phosphonates, and sulfones. (97 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Enzyme
His primary areas of study are Organic chemistry, Stereochemistry, Chemical synthesis, Catalysis and Carbene.
The study of Stereochemistry is intertwined with the study of Ring in a number of ways.
The Chemical synthesis study combines topics in areas such as Amidine and Ethyl diazoacetate.
His Catalysis study combines topics in areas such as Nucleophilic aromatic substitution, Electrophilic aromatic substitution, Photochemistry, Oxygen and Quinazoline.
The concepts of his Carbene study are interwoven with issues in Hydrazide, Medicinal chemistry, Triazine, Rhodium and Copper.
His research in Rhodium intersects with topics in Insertion reaction and Aldol reaction.
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