Research area 01

Synthetic and heterocyclic chemistry

Designing the underlying chemistry, not simply changing the equipment in which it runs.

The group combines mechanistic organic chemistry, inventive route design and practical synthesis to create valuable heterocyclic frameworks and functional molecules. Enabling technology is selected only where it improves the chemistry, control, safety or delivery of the process.

Scientific questions

Questions that shape the work

  1. 01

    How can molecular complexity be assembled with fewer, more selective operations?

  2. 02

    Which ring-forming and functionalisation strategies create differentiated, useful molecular architectures?

  3. 03

    How can challenging intermediates be generated and transformed without compromising selectivity or practicality?

  4. 04

    Where can flow, photochemistry or automation unlock chemistry that is difficult in conventional batch operation?

Established expertise

Demonstrated capabilities

These themes reflect the group’s established scientific record. Availability for a new project depends on scope, collaborators, funding and the practical requirements of the work.

Heterocycle and ring-system constructionCascade and multicomponent transformationsFunctional-group interconversionLate-stage and scaffold functionalisationMedicinally relevant small-molecule synthesisReaction discovery and mechanism-led optimisationMultistep synthesis and route adaptation

Approach

How the problem is addressed

Chemistry, evidence and technology are considered together, with methods selected for scientific value rather than novelty alone.

01

Mechanistic design

Use reaction understanding to guide reagent, catalyst and sequence selection.

02

Scaffold construction

Create saturated, fused and heteroatom-rich architectures with controlled substitution.

03

Technology-enabled synthesis

Introduce continuous flow, light, pressure or automation when these provide a clear chemical advantage.

Representative applications

Where this expertise can contribute

  • Heterocyclic building blocks
  • Medicinal chemistry libraries
  • Fine-chemical intermediates
  • Complex and functional molecular scaffolds

Future research direction

Developing the next programme

Future work will connect synthesis planning, experimentally grounded reaction development and technology selection more tightly, enabling faster evaluation of alternative molecular routes and more decisive progression toward scalable chemistry.

View the future programme

Collaboration opportunity

Discuss a substantive project

Discussions are welcomed around difficult heterocycle construction, constrained route options, medicinally relevant scaffold preparation and technology-enabled synthetic methodology.

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