Chemical synthesis

Cardiff Research Areas»Engineering and Physical Sciences

Subordinate Areas

• Asymmetric Chemistry
  • Asymmetric synthesis
  • C2 symmetric
  • Chiral Auxiliaries
  • Chiral Reagents
  • Desymmetrisation
  • Directed Reactions
  • Enantiomeric Excess
  • Enantiomers
  • Kinetic Resolution
  • Regio-control
  • Resolving Agent
  • Sharpless Reactions
  • Stereochemistry
  • Theoretical Stereochemistry
• Biological and Medicinal Chemistry
  • Alkaloids
  • Allosteric
  • Amino acids
  • Artifical Enzymes
  • Beta Sheet
  • Bio-organic Synthesis
  • Biomimetic Chemistry
  • Biophysical Chemistry
  • Biosites
  • Catalytic Antibodies
  • DNA Chemistry
  • DNA/RNA cleavage
  • Drug Design
  • Enzyme models
  • Fatty Acids
  • Ionophores
  • Lipid synthesis
  • Liposomes
  • Medicinal Bio-catalysis
  • Medicinal Biotransformations
  • Medicinal Chemistry
  • Michaelis-Menten
  • Molecular Gears
  • Natural Product Structures
  • Nucleic Acids
  • Organic Host-guest chemistry
  • Peptide Design
  • Peptide Glycans
  • Peptide Synthesis
  • Polyketides
  • Polymers for Medicinal Use
  • Porphyrins
  • Prebiotic chemistry
  • Protein Structure
  • Shikimic Acids
  • Steroid Chemistry
  • Terpenes
  • Tracer Radioactive Elements
• Chemical Synthetic Methodology
  • Addition Reactions
  • Aldol
  • Alkenes
  • Alkynes
  • Amination Reaction
  • Annulation reactions
  • Arenes
  • Arynes
  • Azides
  • Baeyer-Villiger Reaction
  • Boron reagents
  • Carbenes
  • Carbonylation
  • Cascade Processes
  • Catenanes
  • Claisen rearrangement
  • Cryptands/Cryptates
  • Curtius rearrangment
  • Cycloaddition reactions
  • Cyclophanes
  • Diels-Alder reaction
  • Dihydroxylation
  • Efficient synthesis
  • Ene Reaction
  • Epoxidation
  • Friedel-Crafts
  • Green synthesis
  • Heavy element heterocycles
  • Heck reaction
  • Heterocyclic chemistry
  • High Pressure Synthesis
  • Hydroamination
  • Hydrocarbon activation
  • Hydrothermal Synthesis
  • Imines
  • Inorganic Host-guest chemistry
  • Isomerisation
  • Lanthanide reagents
  • Lithium reagents
  • Macrocycles
  • Magnesium reagents
  • Mannich reaction
  • Metallocenes
  • Metathesis reactions
  • Michael Reaction
  • Mitsunobu Reaction
  • MOF synthesis
  • Molecular Design
  • Natural Product Synthesis
  • Nazarov
  • Nitrenes
  • Olefination
  • Organofluorine
  • Organometallic syntheses
  • Organosilicon reagents
  • Pericyclic Processes
  • Phosphorus reagents
  • Photochemical synthesis
  • Polycyclics
  • Protecting Groups
  • Radical reactions
  • Rearrangements
  • Ring Expansion/Contraction
  • Ring Opening/Closing
  • Rotaxanes
  • Self-assembly
  • Sigmatropic reaction
  • Silicon chemistry
  • Sonochemistry
  • Staudinger reaction
  • Sulfur reagents
  • Supercritical Fluids
  • Supramolecular chemistry
  • Suzuki reaction
  • Total Synthesis
  • Transition metal reagents
  • Vilsmeier reaction
  • Wacker reaction
  • Wittig reaction
• Co-ordination Chemistry
  • Actinide complexes
  • Coordination Complexes
  • Coordination Dendrimers
  • Lanthanide complexes
  • Ligand Design
  • Ligand Synthesis
  • Molecular Complexes Design
  • Molecular switch complexes
  • Organometallic complexes
  • Racemisation
  • Transition metal complexes
• Combinatorial Chemistry
  • Combinatorial Coupling
  • Combinatorial Library Design
  • Dynamic Combinatorial Chem.
  • High Throughput Screening
  • Library Screening Techniques
  • Parallel Synthesis
  • Resin Beads
  • Resin Synthesis
  • Solid Phase Organic Synthesis
  • Solid Supported Scavengers
  • Solid Supports
  • Solution Phase Combinatorial Chemistry
  • Traceless Linker
• Drug Formulation and Delivery
  • Creams for drug delivery
  • Drug Administration
  • Drug Delivery Devices
  • Drug Delivery Implants
  • Drug emulsions
  • Drug nanoparticles
  • Encapsulation of drugs
  • Flocculation of drugs
  • Formulation of Drugs
  • Liposomes for drugs
  • Micelles for drugs
  • Microparticles for drugs
  • Mucosal Surfaces
  • Polymer Drug Conjugates
  • Polymer Therapeutics
  • Vesicles for drugs
• Synthetic biology
  • Artificial Cellular Systems
  • Artificial Vesicles/Capsules
  • Bacterial Integrons
  • Biologically Based Parts
  • Bioprocess Engineering- Synbio
  • Biosensors - Synbio
  • Biotechnology - Synbio
  • Cell Membranes - Synbio
  • Cell Signalling - Synbio
  • Cellular Design
  • Design Tools - Synbio
  • Genetically Engineered Machine
  • Manufacturing - Synbio
  • Minimal Cell
  • Modified Cell
  • Modularity - Synthetic Biology
  • Personalised Medicine
  • Synbio - Drug Development
  • Synbio - Energy/Biofuels
  • Synbio - Materials
  • Synthetic Biology Applications
  • Synthetic Biology Devices
  • Synthetic Biology Methods
  • Synthetic Cell

Projects

Related Datasets

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A quantitative approach to predicting rate constants for aqueous racemization allows pointless stereoselective syntheses to be avoided - Ballard A, Buurma NJ (2017). Cardiff University. 10.17035/d.2017.0043106638. Chemical reaction dynamics and mechanisms Chemical synthesis Catalysis and surfaces Chemical measurement

Borane Catalyzed Stereoselective C–H insertion, Cyclopropanation, and Ring-Opening Reactions - data - Dasgupta A, Babaahmadi R, Slater B, et al. (2020). Cardiff University. 10.17035/d.2020.0111365980. Catalysis and surfaces Chemical synthesis

Chiral carbene–borane adducts: precursors for borenium catalysts for asymmetric FLP hydrogenations - Lam J, Günther BAR, Farrell JM, et al. (2016). Cardiff University. 10.17035/d.2016.0011648516. Chemical synthesis Chemical X-ray Crystallography Chemical Synthetic Methodology Imines

Contrasting frustrated Lewis pair reactivity with selenium- and boron-based Lewis acids - Wilkins LC, Gunther BAR, Walther M, et al. (2017). Cardiff University. 10.17035/d.2017.0011648620. Chemical synthesis

Copper(II) complexes of pyridine-oxazoline (Pyox) ligands: coordination chemistry, ligand stability and catalysis - Ward BD, Hallett AJ, Kariuki B (2016). Cardiff University. 10.17035/d.2015.100130. Chemical synthesis

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Last updated on 2015-10-11 at 12:52