Structure–activity relationships of piperazine scaffolds in CNS drugs
A review of substitution patterns in recent CNS agents, and the balance between basicity, lipophilicity and receptor selectivity.
Read abstract →Chemistry · Pharmacy · Heterocycles
A six-membered nitrogen heterocycle whose conformational flexibility and hydrogen-bonding behaviour make it a privileged scaffold in medicinal chemistry.
Literature notes
Recent reading and experimental notes on piperazine scaffolds, heterocyclic synthesis and medicinal chemistry.
A review of substitution patterns in recent CNS agents, and the balance between basicity, lipophilicity and receptor selectivity.
Read abstract →Comparing catalytic hydrogenation and photoredox routes for selectivity, cost and scalability.
Read abstract →Using single-crystal diffraction data to examine how substituents alter ring conformation and intermolecular interactions.
Read abstract →Research directions
Four long-term interests connecting synthesis, structure and drug design.
Route design, catalysis and process scale-up for piperazine and heterocyclic scaffolds.
Reactivity, conformation and substituent effects in six-membered nitrogen heterocycles.
Structure–activity relationships, pharmacokinetic properties and fragment-based design.
NMR, MS and crystallography in structure elucidation.