Piperazine

Chemistry · Pharmacy · Heterocycles

Piperazine

A six-membered nitrogen heterocycle whose conformational flexibility and hydrogen-bonding behaviour make it a privileged scaffold in medicinal chemistry.

Research notes on piperazine scaffolds, medicinal chemistry, and heterocyclic synthesis.

Literature notes

Latest articles

Recent reading and experimental notes on piperazine scaffolds, heterocyclic synthesis and medicinal chemistry.

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 →

Green synthetic routes and catalyst selection for heterocyclic amines

Comparing catalytic hydrogenation and photoredox routes for selectivity, cost and scalability.

Read abstract →

Hydrogen-bonding networks in piperazine derivatives from crystal structures

Using single-crystal diffraction data to examine how substituents alter ring conformation and intermolecular interactions.

Read abstract →

Research directions

Research directions

Four long-term interests connecting synthesis, structure and drug design.

Drug Synthesis

Route design, catalysis and process scale-up for piperazine and heterocyclic scaffolds.

Heterocyclic Chemistry

Reactivity, conformation and substituent effects in six-membered nitrogen heterocycles.

Medicinal Chemistry

Structure–activity relationships, pharmacokinetic properties and fragment-based design.

Analytical Characterization

NMR, MS and crystallography in structure elucidation.