Department of Chemistry

portrait of Dr David Spring

Dr David Spring

Trinity College

Groups: Spring group website

Telephone: 01223 336498

E-mail: spring@ch.cam.ac.uk

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.

Selected Publications

For our most recent publications please visit the Spring Group publication page.

Diversity-Oriented Synthesis of Macrocyclic Peptidomimetics. Proc. Natl. Acad. Sci. USA 2011108, 6793-6798.
Better leads come from diversity. Nature 2011470, 43.
Novel and Efficient Copper-Catalysed Synthesis of Nitrogen-Linked Medium-Ring Biaryls. Chem. Eur. J. 201117, 2981-2986.
Chemical Genetics. Chem. Soc. Rev. 201140, 4332-4345.
Diversity-oriented synthesis as a tool for the discovery of novel biologically functional small molecules. Nature Commun. 20101, 80.
Zn2+-Triggered Amide Tautomerization Produces a Highly Zn2+-Selective, Cell-Permeable and Ratiometric Fluorescent Sensor. JACS 2010, 132, 601-610.
Diversity-oriented synthesis of bicyclic and tricyclic alkaloids. Chem. Commun. 201046, 776-778.
The molecular basis of the host response to lipopolysaccharide. Nature Rev. Microbio. 2010, 8, 8-14.
3D small-molecule microarrays. Chem. Commun. 2009, 7107-7109.
Mastering the Chemical Language of Bacteria. Chem. Biol. 2009, 16, 913-914.
The discovery of antibacterial agents using diversity oriented synthesis. Chem. Commun. 2009, 2446-2462.
Synthesis of Unprecedented Scaffold Diversity. Angew. Chem. Int. Ed. 2009, 48, 1194-1196.
Towards quorum-quenching catalytic antibodies. Chem. Commun. 2009, 538-540.
Total Synthesis of Sanguiin H-5. Org. Lett. 2008, 10, 2593-2596.
Anti-MRSA Agent Discovery Using Diversity-Oriented Synthesis. Angew. Chem. Int. Ed. 2008, 47, 2808-2812.

 


General


 

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

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.

Personal


 

For more detailed information please visit here.

Publications

 

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

Publications

A quorum-sensing molecule acts as a morphogen controlling gas vesicle organelle biogenesis and adaptive flotation in an enterobacterium
JP Ramsay, NR Williamson, DR Spring, GPC Salmond - Proceedings of the National Academy of Sciences of the United States of America (2011) 108, 14932
(DOI: 10.1073/pnas.1109169108)
Stereoselective Synthesis of Disubstituted Butadienes via Copper-Mediated Coupling of Alkenyl Silanes
DT Blackwell, WRJD Galloway, DR Spring - Synlett (2011), 2140
(DOI: 10.1055/s-0030-1261150)
Small molecules in biology
A Tavassoli, AD Hamilton, DR Spring - Chemical Society Reviews (2011) 40, 4269
(DOI: 10.1039/c1cs90028e)
Fluorescent sensing and discrimination of ATP and ADP based on a unique sandwich assembly of pyrene-adenine-pyrene.
Z Xu, DR Spring, J Yoon - Chem Asian J (2011) 6, 2114
(DOI: 10.1002/asia.201100120)
Efficient Synthesis of Fmoc-Protected Azido Amino Acids
YH Lau, DR Spring - Synlett (2011), 1917
(DOI: 10.1055/s-0030-1260950)
Chemogenomics approaches for receptor deorphanization and extensions of the chemogenomics concept to phenotypic space
E van der Horst, JE Peironcely, GJP van Westen, OO van den Hoven, WRJD Galloway, DR Spring, JK Wegner, HWT van Vlijmen, AP IJzerman, JP Overington, A Bender - Current Topics in Medicinal Chemistry (2011) 11, 1964
Chemical genetics
CJO Connor, L Laraia, DR Spring - Chemical Society Reviews (2011) 40, 4332
(DOI: 10.1039/c1cs15053g)
Robust routes for the synthesis of N-acylated-L-homoserine lactone (AHL) quorum sensing molecules with high levels of enantiomeric purity
JT Hodgkinson, WRJD Galloway, M Casoli, H Keane, XB Su, GPC Salmond, M Welch, DR Spring - Tetrahedron Letters (2011) 52, 3291
(DOI: 10.1016/j.tetlet.2011.04.059)
Regioselectivity in Thermal Rhodium(II)-Catalysed Büchner-Type Reactions of Substituted Aryl Halides: Studies towards the Synthesis of Halide-Substituted Cycloheptatrienes
EE Wyatt, WRJD Galloway, DR Spring - Synlett (2011), 1449
(DOI: 10.1055/s-0030-1260562)
The Serratia LuxR family regulator CarR 39006 activates transcription independently of cognate quorum sensing signals.
S Poulter, TM Carlton, DR Spring, GPC Salmond - Mol Microbiol (2011) 80, 1120
(DOI: 10.1111/j.1365-2958.2011.07634.x)
Diversity-oriented synthesis of macrocyclic peptidomimetics
A Isidro-Llobet, T Murillo, P Bello, A Cilibrizzi, JT Hodgkinson, WRJD Galloway, A Bender, M Welch, DR Spring - Proceedings of the National Academy of Sciences of the United States of America (2011) 108, 6793
(DOI: 10.1073/pnas.1015267108)
Controlling the contents of microdroplets by exploiting the permeability of PDMS
JU Shim, SN Patil, JT Hodgkinson, SD Bowden, DR Spring, M Welch, WTS Huck, F Hollfelder, C Abell - Lab on a Chip - Miniaturisation for Chemistry and Biology (2011) 11, 1132
(DOI: 10.1039/C0LC00615G)
Rational methods for the selection of diverse screening compounds
DJ Huggins, AR Venkitaraman, DR Spring - ACS Chem Biol (2011) 6, 208
(DOI: 10.1021/cb100420r)
Novel and efficient copper-catalysed synthesis of nitrogen-linked medium-ring biaryls
JL Kenwright, WRJD Galloway, DT Blackwell, A Isidro-Llobet, J Hodgkinson, L Wortmann, SD Bowden, M Welch, DR Spring - Chemistry (2011) 17, 2981
(DOI: 10.1002/chem.201002093)
Drug discovery: A question of library design.
PJ Hajduk, WR Galloway, DR Spring - Nature (2011) 470, 42
(DOI: 10.1038/470042a)
Better leads come from diversity
WRJD Galloway, DR Spring - NATURE (2011) 470, 43
Induction-driven stabilization of the anion-π interaction in electron-rich aromatics as the key to fluoride inclusion in imidazolium-cage receptors.
Z Xu, NJ Singh, SK Kim, DR Spring, KS Kim, J Yoon - Chemistry (2011) 17, 1163
(DOI: 10.1002/chem.201002105)
Vinyldisiloxanes: their synthesis, cross coupling and applications
HF Sore, CM Boehner, L Laraia, P Logoteta, C Prestinari, M Scott, K Williams, WRJD Galloway, DR Spring - Organic and Biomolecular Chemistry (2011) 9, 504
(DOI: 10.1039/c0ob00338g)
Quorum Sensing in Gram-Negative Bacteria: Small-Molecule Modulation of AHL and Al-2 Quorum Sensing Pathways
WRJD Galloway, JT Hodgkinson, SD Bowden, M Welch, DR Spring - Chem Rev (2011) 111, 28
(DOI: 10.1021/cr100109t)
Microwave and flow syntheses of Pseudomonas quinolone signal (PQS) and analogues.
JT Hodgkinson, WRJD Galloway, S Saraf, IR Baxendale, SV Ley, M Ladlow, M Welch, DR Spring - Organic and Biomolecular Chemistry (2011) 9, 57
(DOI: 10.1039/c0ob00652a)
The Serratia LuxR family regulator CarR 39006 activates transcription independently of cognate quorum sensing signals
S Poulter, TM Carlton, DR Spring, GP Salmond - Molecular Microbiology (2011) 80, 1120
Synthesis of Highly Substituted Symmetrical 1,3-Dienes via Organocuprate Oxidation
SJ Aves, KM O'Connell, KG Pike, DR Spring - Synlett (2011)
Stereoselective synthesis of disubstituted butadienes via copper-mediated coupling of alkenyl silanes
DT Blackwell, WRJD Galloway, DR Spring - Synlett (2011), 2140
Robust routes for the synthesis of N-acylated-l-homoserine lactone (AHL) quorum sensing molecules with high levels of enantiomeric purity
JT Hodgkinson, WRJD Galloway, M Casoli, H Keane, X Su, GPC Salmond, M Welch, DR Spring - Tetrahedron Letters (2011) 52, 3291
Regioselectivity in thermal rhodium(II)-catalysed Büchner-type reactions of substituted aryl halides: Studies towards the synthesis of halide-substituted cycloheptatrienes
EE Wyatt, WRJD Galloway, DR Spring - Synlett (2011), 1449

Funding


Funding: 

 

We are extremely fortunate, and grateful, that this research is funded by research councils (A*Star, BBSRC, DAAD, EPSRC, ERC, EU, MRC), charities (CRUK, Cambridge Trusts, Frances and Augustus Newman Foundation, Isaac Newton Trust, Wellcome Trust) and industry (AZ, Bayer Schering, GSK, Lilly, Pfizer, Syngenta, UCB).

CV

CV: 

 

For more detailed information please visit here.