What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Stereochemistry
Anthony C. Willis spends much of his time researching Stereochemistry, Medicinal chemistry, Organic chemistry, Crystallography and Crystal structure.
He has included themes like Phosphine, Ligand and Stereoisomerism in his Stereochemistry study.
His Ligand study combines topics from a wide range of disciplines, such as Nuclear magnetic resonance spectroscopy, Metal, Benzene and Diastereomer.
His Medicinal chemistry research integrates issues from Boron, Palladium, Inorganic chemistry, Ruthenium and Carbyne.
He has researched Crystallography in several fields, including X-ray crystallography, Molecule and Copper.
His work carried out in the field of Total synthesis brings together such families of science as Derivative, Aryl and Intramolecular force.
His most cited work include:
- Calothrixins A and B, novel pentacyclic metabolites from Calothrix cyanobacteria with potent activity against malaria parasites and human cancer cells (159 citations)
- Organometallic Complexes for Nonlinear Optics. 22.1 Quadratic and Cubic Hyperpolarizabilities of trans-Bis(bidentate phosphine)ruthenium σ-Arylvinylidene and σ-Arylalkynyl Complexes (101 citations)
- Metallaboratranes: Tris(methimazolyl)borane Complexes of Rhodium(I) (93 citations)
What are the main themes of his work throughout his whole career to date?
Anthony C. Willis mainly focuses on Stereochemistry, Crystal structure, Crystallography, Medicinal chemistry and Organic chemistry.
His research in Stereochemistry intersects with topics in Molecule and Ligand.
His research integrates issues of X-ray crystallography and Cobalt in his study of Crystal structure.
His Crystallography research is multidisciplinary, relying on both Metal and Copper.
His work deals with themes such as Phosphine, Catalysis, Ruthenium, Palladium and Inorganic chemistry, which intersect with Medicinal chemistry.
His study involves Cycloaddition, Adduct and Derivative, a branch of Organic chemistry.
He most often published in these fields:
- Stereochemistry (49.00%)
- Crystal structure (24.36%)
- Crystallography (23.65%)
What were the highlights of his more recent work (between 2014-2021)?
- Stereochemistry (49.00%)
- Organic chemistry (18.95%)
- Crystallography (23.65%)
In recent papers he was focusing on the following fields of study:
Stereochemistry, Organic chemistry, Crystallography, Combinatorial chemistry and Total synthesis are his primary areas of study.
His Stereochemistry study combines topics from a wide range of disciplines, such as Molecule and Cycloaddition.
He is involved in the study of Crystallography that focuses on Crystal structure in particular.
Anthony C. Willis has included themes like Electrophile, Ring, Propargyl, Cascade and Aryl in his Combinatorial chemistry study.
His work investigates the relationship between Total synthesis and topics such as Biotransformation that intersect with problems in Toluene and Diels alder.
Anthony C. Willis works mostly in the field of Intramolecular force, limiting it down to concerns involving Catalysis and, occasionally, Nano- and Medicinal chemistry.
Between 2014 and 2021, his most popular works were:
- Pseudopterosin synthesis from a chiral cross-conjugated hydrocarbon through a series of cycloadditions (37 citations)
- Synthesis and characterisation of nickel Schiff base complexes containing the meso-1,2-diphenylethylenediamine moiety: selective interactions with a tetramolecular DNA quadruplex (29 citations)
- Spectroscopic and TD-DFT studies on the turn-off fluorescent chemosensor based on anthraldehyde N(4) cyclohexyl thiosemicarbazone for the selective recognition of fluoride and copper ions (27 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
His primary scientific interests are in Stereochemistry, Organic chemistry, Intramolecular force, Total synthesis and Molecule.
His work carried out in the field of Stereochemistry brings together such families of science as Adduct and Stereoisomerism.
His research in the fields of Macrolide formation overlaps with other disciplines such as Nicandrenone.
The concepts of his Total synthesis study are interwoven with issues in Sequence, Pseudopterosins, Biotransformation and Hydrocarbon.
His Molecule study integrates concerns from other disciplines, such as Crystallography, Photochemistry, Piperidine and Fluorescence.
His Crystallography study combines topics in areas such as Molybdenum compounds, Molybdenum, Rhenium, Solvent effects and Thioether.
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