skip to content
 

Professor David Spring

Portrait of drs36

Our research interests originate from a desire to understand and exploit biological systems using organic synthesis primarily. Listed below are areas of research that we are exploring; for more detailed information visit the Spring Group web pages.

• Diversity-Oriented Synthesis
• Synthetic Methodology: Medium Ring Synthesis and Natural Product Synthesis
Quorum Sensing
• New Antibiotic Discovery
• Modulation of Protein-Protein Interactions
• Molecular Therapeutics: Chemistry-Driven Drug Discovery

We collaborate with many chemical companies and academic groups around the world. The scientific education of group members in organic synthesis is given a high priority; however, they are encouraged also to learn and perform new techniques relating to their projects with our industrial and academic collaborators. Every effort is made so that group members achieve their career ambitions, usually jobs in academia or the chemical industries.

Research Interests

For more detailed information please visit the Spring Group research pages.

 

Teaching

If you are looking for the teaching material from my lecture courses, then please go to the CamTools website.

 

Publications

For a list of all our publications please visit the Spring Group publication page.

Publications

Synthesis of a novel polycyclic ring scaffold with antimitotic properties via a selective domino Heck-Suzuki reaction
E Alza, L Laraia, BM Ibbeson, S Collins, WRJD Galloway, JE Stokes, AR Venkitaraman, DR Spring – Chem. Sci. (2014) 6, 390
Studies towards the synthesis of indolizin-5(3H)-one derivatives and related 6,5-azabicyclic scaffolds by ring-closing metathesis.
MS Frei, MK Bilyard, TA Alanine, WR Galloway, JE Stokes, DR Spring – Bioorganic & medicinal chemistry (2014)
Multifunctional supramolecular polymer networks as next-generation consolidants for archaeological wood conservation
Z Walsh, ER Janeček, JT Hodgkinson, J Sedlmair, A Koutsioubas, DR Spring, M Welch, CJ Hirschmugl, C Toprakcioglu, JR Nitschke, M Jones, OA Scherman – Proceedings of the National Academy of Sciences of the United States of America (2014) 111, 17743
Linear aliphatic dialkynes as alternative linkers for double-click stapling of p53-derived peptides.
YH Lau, P de Andrade, GJ McKenzie, AR Venkitaraman, DR Spring – Chembiochem (2014) 15, 2680
Diversity-Oriented Synthesis of Drug-Like Macrocyclic Scaffolds Using an Orthogonal Organo- and Metal Catalysis Strategy
A Grossmann, S Bartlett, M Janecek, JT Hodgkinson, DR Spring – Angew Chem Int Ed Engl (2014) 53, 13093
Peptide stapling techniques based on different macrocyclisation chemistries.
YH Lau, P de Andrade, Y Wu, DR Spring – Chemical Society reviews (2014) 44, 91
Toxicity of six plant extracts and two pyridone alkaloids from Ricinus communis against the malaria vector Anopheles gambiae
SW Wachira, S Omar, JW Jacob, M Wahome, HT Alborn, DR Spring, DK Masiga, B Torto – Parasites & vectors (2014) 7, 312
Arene C-H functionalisation using a removable/modifiable or a traceless directing group strategy.
F Zhang, DR Spring – Chemical Society reviews (2014) 43, 6906
The Use of Chlorobenzene as a Probe Molecule in Molecular Dynamics Simulations
YS Tan, DR Spring, C Abell, C Verma – J Chem Inf Model (2014) 54, 1821
Investigating peptide sequence variations for ‘double-click’ stapled p53 peptides
YH Lau, P de Andrade, N Sköld, GJ McKenzie, AR Venkitaraman, C Verma, DP Lane, DR Spring – Org Biomol Chem (2014) 12, 4074
  •  
  • 1 of 19
  • >

Research Group

Research Interest Group

Telephone number

01223 336498

Email address

spring@ch.cam.ac.uk