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Yusuf Hamied Department of Chemistry

 

Professor of Chemistry & Chemical Biology / EPSRC Established Career Research Fellow

 

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.

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.

Spring Group Figure

 

 

Watch Professor David Spring discuss his research

Take a quick tour of the Spring Lab

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 Moodle website.

Publications

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

Publications

Cycloaddition Strategies for the Synthesis of Diverse Heterocyclic Spirocycles for Fragment-Based Drug Discovery.
TA King, HL Stewart, KT Mortensen, AJP North, HF Sore, DR Spring
– European Journal of Organic Chemistry
(2019)
2019,
5219
Hotspots API: a toolkit for the application of fragment hotspot mapping to structure-based drug discovery
P Curran, C Radoux, M Smilova, A Higueruelo, R Sykes, A Bradley, W Pitt, D Spring, T Blundell, J Cole
– Acta Crystallographica Section A: Foundations and advances
(2019)
75,
A227
Macrocyclisation and functionalisation of unprotected peptides: Via divinyltriazine cysteine stapling
NS Robertson, SJ Walsh, E Fowler, M Yoshida, SM Rowe, Y Wu, HF Sore, JS Parker, DR Spring
– Chemical communications (Cambridge, England)
(2019)
55,
9499
Targeted covalent inhibitors of MDM2 using electrophile-bearing stapled peptides.
J Charoenpattarapreeda, YS Tan, J Iegre, SJ Walsh, E Fowler, RS Eapen, Y Wu, HF Sore, CS Verma, L Itzhaki, DR Spring
– Chemical communications (Cambridge, England)
(2019)
55,
7914
Strategies for the Diversity-Oriented Synthesis of Macrocycles
KT Mortensen, TJ Osberger, TA King, HF Sore, DR Spring
– Chemical reviews
(2019)
119,
10288
Cleavable linkers in antibody–drug conjugates
JD Bargh, A Isidro-Llobet, JS Parker, DR Spring
– Chem Soc Rev
(2019)
48,
4361
Spirocycles as Rigidified sp3-Rich Scaffolds for a Fragment Collection
A Sveiczer, AJP North, N Mateu, SL Kidd, HF Sore, DR Spring
– Organic letters
(2019)
21,
4600
Efficient development of stable and highly functionalised peptides targeting the CK2α/CK2β protein-protein interaction
J Iegre, P Brear, DJ Baker, YS Tan, EL Atkinson, HF Sore, DH O' Donovan, CS Verma, M Hyvönen, DR Spring
– Chemical science
(2019)
10,
5056
Toolbox of Diverse Linkers for Navigating the Cellular Efficacy Landscape of Stapled Peptides
Y Wu, A Kaur, E Fowler, MM Wiedmann, R Young, WRJD Galloway, L Olsen, HF Sore, A Chattopadhyay, TT-L Kwan, W Xu, SJ Walsh, P de Andrade, M Janecek, S Arumugam, LS Itzhaki, YH Lau, DR Spring
– ACS Chem Biol
(2019)
14,
526
Synthesis and Reactivity of a Bis-Strained Alkyne Derived from 1,1'-Biphenyl-2,2',6,6'-tetrol.
RC Knighton, K Sharma, NS Robertson, DR Spring, M Wills
– ACS Omega
(2019)
4,
2160
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Research Group

Research Interest Groups

Telephone number

01223 336498

Email address

spring@ch.cam.ac.uk