Department of Chemistry

portrait of Professor David Spring

Professor 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

Structure-activity relationships of Erwinia carotovora quorum sensing signaling molecules
M Welch, JM Dutton, FG Glansdorp, GL Thomas, DS Smith, SJ Coulthurst, AML Barnard, GPC Salmond, DR Spring - Bioorg Med Chem Lett (2005) 15, 4235
(DOI: 10.1016/j.bmcl.2005.06.066)
Cell-cell communication in gram-negative bacteria
M Welch, H Mikkelsen, JE Swatton, D Smith, GL Thomas, FG Glansdorp, DR Spring - Molecular BioSystems (2005) 1, 196
(DOI: 10.1039/b505796p)
Chemical genetics to chemical genomics: Small molecules offer big insights
DR Spring - Chemical Society Reviews (2005) 34, 472
(DOI: 10.1039/b312875j)
Assessment of structural diversity in combinatorial synthesis.
S Fergus, A Bender, DR Spring - Curr Opin Chem Biol (2005) 9, 304
(DOI: 10.1016/j.cbpa.2005.03.004)
Aryl-aryl coupling via directed lithiation and oxidation.
DS Surry, DJ Fox, SJF Macdonald, DR Spring - Chemical Communications (2005), 2589
(DOI: 10.1039/b501939g)
Synthesis of medium-ring and iodinated biaryl compounds by organocuprate oxidation
DS Surry, XB Su, DJ Fox, V Franckevicius, SJF Macdonald, DR Spring - Angew Chem Int Ed Engl (2005) 44, 1870
(DOI: 10.1002/anie.200462642)
Erratum: Synthesis of medium-ring and iodinated biaryl compounds by organocuprate oxidation (Angewandte Chemie International Edition (2005) 44 (1870-1873) DOI: 10.1002/anie.200462642)
DS Surry, X Su, DJ Fox, V Franckevicius, SJF Macdonald, DR Spring - Angewandte Chemie - International Edition (2005) 44, 2471
Finding new components of the target of rapamycin (TOR) signaling network through chemical genetics and proteome chips
J Huang, H Zhu, SJ Haggarty, DR Spring, H Hwang, FL Jin, M Snyder, SL Schreiber - Proceedings of the National Academy of Sciences (2004) 101, 16594
(DOI: 10.1073/pnas.0407117101)
Synthesis and stability of small molecule probes for Pseudomonas aeruginosa quorum sensing modulation
FG Glansdorp, GL Thomas, JJK Lee, JM Dutton, GPC Salmond, M Welch, DR Spring - Organic and Biomolecular Chemistry (2004) 2, 3329
(DOI: 10.1039/B412802H)
Communications blackout? Do N-acylhomoserine lactone-degrading enzymes have any role in quorum sensing?
DM Roche, JT Byers, DS Smith, FG Glansdorp, DR Spring, M Welch - Microbiology (2004) 150, 2023
(DOI: 10.1099/mic.0.26977-0)
Complete functionalisation of small and large diameter bromopolystyrene beads; applications for solid-supported reagents, scavengers and diversity-oriented synthesis
GL Thomas, M Ladlow, DR Spring - Organic and Biomolecular Chemistry (2004) 2, 1679
(DOI: 10.1039/b406488g)
Organocuprate oxidation with improved functional group tolerance and its application to medium ring synthesis
DS Surry, DR Spring - ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY (2004) 227, U118
Highlights from the 39th ESF/EUCHEM Conference on Stereochemistry, Bürgenstock, Switzerland, April 2004
CJ Hayes, DR Spring - Chemical Communications (2004) 10, 2365
Finding new components of the target of rapamycin (TOR) signaling network through chemical genetics and proteome chips
J Huang, H Zhu, SJ Haggarty, DR Spring, H Hwang, F Jin, M Snyder, SL Schreiber - Proceedings of the National Academy of Sciences of the United States of America (2004) 101, 16594
Diversity-oriented synthesis; a challenge for synthetic chemists.
DR Spring - Organic and Biomolecular Chemistry (2003) 1, 3867
(DOI: 10.1039/b310752n)
How diverse is your combinatorial library?
DR Spring - ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY (2003) 225, U280
Diversity-oriented synthesis of biaryl-containing medium rings using a one bead/one stock solution platform
DR Spring, S Krishnan, HE Blackwell, SL Schreiber - Journal of the American Chemical Society (2002) 124, 1354
(DOI: 10.1021/ja017248o)
A one-bead, one-stock solution approach to chemical genetics: Part 2
PA Clemons, AN Koehler, BK Wagner, TG Sprigings, DR Spring, RW King, SL Schreiber, MA Foley - Chemistry & Biology (2001) 8, 1183
(DOI: 10.1016/S1074-5521(01)00086-2)
Towards diversity-oriented, stereoselective syntheses of biaryl- or bis(aryl)metal-containing medium rings [11]
DR Spring, S Krishnan, SL Schreiber - Journal of the American Chemical Society (2000) 122, 5656
(DOI: 10.1021/ja0010507)
Studies on the biomimetic synthesis of the manzamine alkaloids
JE Baldwin, TDW Claridge, AJ Culshaw, FA Heupel, V Lee, DR Spring, RC Whitehead - Chemistry - A European Journal (1999) 5, 3154
(DOI: 10.1002/(SICI)1521-3765(19991105)5:11<3154::AID-CHEM3154>3.0.CO;2-7)
Efficient synthesis of the sponge alkaloids cyclostellettamines A-F
JE Baldwin, DR Spring, CE Atkinson, V Lee - Tetrahedron (1998) 54, 13655
(DOI: 10.1016/S0040-4020(98)00842-4)
A novel Diels-Alder approach to hydroisoquinolines
JE Baldwin, DR Spring, RC Whitehead - Tetrahedron Letters (1998) 39, 5417
(DOI: 10.1016/S0040-4039(98)01043-0)
Investigations into the manzamine alkaloid biosynthetic hypothesis
JE Baldwin, TDW Ciaridge, AJ Culshaw, FA Heupel, V Lee, DR Spring, RC Whitehead, RJ Boughtflower, IM Mutton, RJ Upton - Angewandte Chemie - International Edition (1998) 37, 2661
(DOI: 10.1002/(SICI)1521-3773(19981016)37:19<2661::AID-ANIE2661>3.3.CO;2-4)
A biomimetic approach to the manzamine alkaloids
DR Spring, JE Baldwin, RC Whitehead, L Bischoff, TDW Claridge - FASEB Journal (1997) 11, A894
An approach to the manzamine alkaloids modelled on a biogenetic theory
JE Baldwin, L Bischoff, DW Claridge, FA Heupel, DR Spring, RC Whitehead - Tetrahedron (1997) 53, 2271
(DOI: 10.1016/S0040-4020(96)01129-5)

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.