Chemical synthesis
Is-feysydd
- Asymmetric Chemistry
- 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
- Combinatorial Chemistry
- 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
Prosiectau
Setiau Data Cysylltiedig
- Accessing Highly Substituted Indoles via B(C6F5)3-Catalyzed Secondary Alkyl Group Transfer - data - Elsherbeni S, Melen R, Pulis A, et al. (2023). Cardiff University. 10.17035/d.2023.0296158061. Chemical synthesis
- 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
- B(C6F5)3-Catalyzed (E)-Selective Isomerization of Alkenes: data - Kustiana BA, Elsherbeni SA, Linford-Wood TG, et al. (2022). Cardiff University. 10.17035/d.2022.0216695569. Chemical synthesis
- 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