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

Novel Phosphate Derivatives as Scaffolds for the Preparation of Synthetic Phosphoserine-Based Peptides Using the Fmoc/t-Bu Solid-Phase Strategy
A Cilibrizzi, A Isidro-Llobet, N Mateu, WR Galloway, DR Spring - Synlett (2011)
Importance of relative humidity in the oxidative ageing of organic aerosols: Case study of the ozonolysis of maleic acid aerosol
PJ Gallimore, P Achakulwisut, FD Pope, JF Davies, DR Spring, M Kalberer - Atmospheric Chemistry and Physics (2011) 11, 12181
(DOI: 10.5194/acp-11-12181-2011)
Importance of relative humidity in the oxidative ageing of organic aerosols: Case study of the ozonolysis of maleic acid aerosol
PJ Gallimore, P Achakulwisut, FD Pope, J Davies, DR Spring, M Kalberer - Atmospheric Chemistry and Physics Discussions (2011) 11, 23169
Erratum: Structure of a blinkin-BUBR1 complex reveals an interaction crucial for kinetochore-mitotic checkpoint regulation via an unanticipated binding site (Structure (2011) 19 (1691-1700))
VM Bolanos-Garcia, T Lischetti, D Matak-Vinković, E Cota, PJ Simpson, DY Chirgadze, DR Spring, CV Robinson, J Nilsson, TL Blundell - Structure (2011) 19, 1895
Efficient synthesis of Fmoc-protected azido amino acids
YH Lau, DR Spring - Synlett (2011), 1917
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 (2010) 17, 1163
(DOI: 10.1002/chem.201002105)
Discovery of a quorum sensing modulator pharmacophore by 3D small-molecule microarray screening.
DM Marsden, RL Nicholson, ME Skindersoe, WRJD Galloway, HF Sore, M Givskov, GPC Salmond, M Ladlow, M Welchd, DR Spring - Organic and Biomolecular Chemistry (2010) 8, 5313
(DOI: 10.1039/c0ob00300j)
Synthesis of Highly Substituted Symmetrical 1,3-Dienes via Tandem Carbocupration and Organocuprate Oxidation
SJ Aves, KG Pike, DR Spring - Synlett (2010), 2839
(DOI: 10.1055/s-0030-1259024)
High throughput 'catch-and-release' synthesis within spatially discrete gel arrays
CM Boehner, DM Marsden, HF Sore, D Norton, DR Spring - Tetrahedron Letters (2010) 51, 5930
(DOI: 10.1016/j.tetlet.2010.09.024)
Discovery of a highly selective turn-on fluorescent probe for Ag+
ZC Xu, SJ Zheng, JY Yoon, DR Spring - Analyst (2010) 135, 2554
(DOI: 10.1039/c0an00405g)
Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules
WRJD Galloway, A Isidro-Llobet, DR Spring - Nature Communications (2010) 1, ARTN 80
(DOI: 10.1038/ncomms1081)
Diversity-oriented synthesis utilizing a two-directional macrocyclisation approach
KMG O'Connell, HT Horsley, DR Spring - ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY (2010) 240
Diversity-oriented synthesis of macrocyclic peptidomimetic scaffolds
A Isidro-Llobet, P Bello, T Murillo, DR Spring - ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY (2010) 240
Diastereoselective 2-aza-Cope rearrangements and their applications in diversity-oriented synthesis
BM Ibbeson, DT Blackwell, DR Spring - ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY (2010) 240
Adventures in diversity-oriented synthesis
WRJD Galloway, DR Spring - ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY (2010) 240
Structure-activity analysis of the Pseudomonas quinolone signal molecule
J Hodgkinson, SD Bowden, WRJD Galloway, DR Spring, M Welch - Journal of Bacteriology (2010) 192, 3833
(DOI: 10.1128/JB.00081-10)
Diversity-Oriented Synthesis of Disubstituted Alkenes Using Masked Silanols
HF Sore, DT Blackwell, SJF MacDonald, DR Spring - Organic Letters (2010) 12, 2806
(DOI: 10.1021/ol100895d)
Fluorescent chemosensors for Zn2+
ZC Xu, J Yoon, DR Spring - Chemical Society Reviews (2010) 39, 1996
(DOI: 10.1039/b916287a)
A selective and ratiometric Cu2+ fluorescent probe based on naphthalimide excimer-monomer switching
ZC Xu, J Yoon, DR Spring - Chemical Communications (2010) 46, 2563
(DOI: 10.1039/c000441c)
Engineering of new prodigiosin-based biosensors of Serratia for facile detection of short-chain N-acyl homoserine lactone quorum-sensing molecules
S Poulter, TM Carlton, XB Su, DR Spring, GPC Salmond - Environmental Microbiology Reports (2010) 2, 322
(DOI: 10.1111/j.1758-2229.2010.00140.x)
Development of off-on fluorescent probes for heavy and transition metal ions
ZC Xu, SJ Han, C Lee, J Yoon, DR Spring - Chemical Communications (2010) 46, 1679
(DOI: 10.1039/b924503k)
Ratiometric fluorescent and colorimetric sensors for Cu2+ based on 4,5-disubstituted-1,8-naphthalimide and sensing cyanide via Cu2+ displacement approach
ZC Xu, J Pan, DR Spring, JN Cui, J Yoon - TETRAHEDRON (2010) 66, 1678
(DOI: 10.1016/j.tet.2010.01.008)
Diversity-oriented synthesis of bicyclic and tricyclic alkaloids.
M Diaz-Gavilan, WRJD Galloway, KMG O'Connell, JT Hodkingson, DR Spring - Chemical Communications (2010) 46, 776
(DOI: 10.1039/b917965h)
Zn2+-Triggered Amide Tautomerization Produces a Highly Zn2+-Selective, Cell-Permeable, and Ratiometric Fluorescent Sensor
ZC Xu, KH Baek, HN Kim, JN Cui, XH Qian, DR Spring, I Shin, J Yoon - J Am Chem Soc (2010) 132, 601
(DOI: 10.1021/ja907334j)
Zn2+-triggered amide tautomerization produces a highly Zn 2+-selective, cell-permeable, and ratiometric fluorescent sensor
Z Xu, K-H Baek, HN Kim, J Cui, X Qian, DR Spring, I Shin, J Yoon - Journal of the American Chemical Society (2010) 132, 601

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.