Professor Steve Ley CBE FRS FMedSci | Page 10 | Yusuf Hamied Department of Chemistry

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Director of Research

In the Ley Group, we specialise in developing new synthesis methods and applying them to the construction of biologically important molecules. Over the last 10 years we have completed the total synthesis of 28 natural products including spongistatin 1 (anti-mitotic agent), rapamycin (immunosuppressant), thapsigargin (SERCA pumps inhibitor), azadirachtin (insect antifeedant) and bengazole A (fungicide), taking our group total to 150 completed total syntheses. In addition to our research on natural product synthesis, we also have a new state-of-the-art flow chemistry facility.

For more detailed research information, group members and our publication list please see the group website.

Publications

Enabling Technologies for the Future of Chemical Synthesis

DE Fitzpatrick, C Battilocchio, SV Ley

– ACS central science

(2016)

2,

131

(doi: 10.1021/acscentsci.6b00015)

Iterative reactions of transient boronic acids enable sequential C-C bond formation

C Battilocchio, F Feist, A Hafner, M Simon, DN Tran, DM Allwood, DC Blakemore, SV Ley

– Nature Chemistry

(2016)

8,

360

(doi: 10.1038/NCHEM.2439)

Synthesis of Natural and Unnatural Cyclooligomeric Depsipeptides Enabled by Flow Chemistry

D Lücke, T Dalton, SV Ley, ZE Wilson

– Chemistry – A European Journal

(2016)

22,

4206

(doi: 10.1002/chem.201504457)

A multistep continuous flow synthesis machine for the preparation of pyrazolesviaa metal-free amine-redox process

J-S Poh, DL Browne, SV Ley

– Reaction Chemistry and Engineering

(2016)

1,

101

(doi: 10.1039/c5re00082c)

Correction: Controlled generation and use of CO in flow

SVF Hansen, ZE Wilson, T Ulven, SV Ley

– Reaction Chemistry & Engineering

(2016)

1,

340

(doi: 10.1039/c6re90010k)

Editorial – Flow Chemistry and Catalysis

SV Ley

– Catalysis Science and Technology

(2016)

6,

4676

(doi: 10.1039/c6cy90064j)

Online quantitative mass spectrometry for the rapid adaptive optimisation of automated flow reactors

N Holmes, GR Akien, RJD Savage, C Stanetty, IR Baxendale, AJ Blacker, BA Taylor, RL Woodward, RE Meadows, RA Bourne

– Reaction Chemistry and Engineering

(2016)

1,

96

(doi: 10.1039/c5re00083a)

Controlled generation and use of CO in flow

SVF Hansen, ZE Wilson, T Ulven, SV Ley

– Reaction Chemistry and Engineering

(2016)

1,

280

(doi: 10.1039/c6re00020g)

Welcome to Reaction Chemistry & Engineering

SA Khan, IR Baxendale, JM Hawkins, SV Ley, K Jensen, V Hessel, G Luo, D Blackmond, A Katz, DG Vlachos, ME Davis

– Reaction Chemistry & Engineering

(2016)

1,

8

(doi: 10.1039/c6re90001a)

Continuous photochemistry: The flow synthesis of ibuprofen: Via a photo-Favorskii rearrangement

M Baumann, IR Baxendale

– Reaction Chemistry and Engineering

(2016)

1,

147

(doi: 10.1039/c5re00037h)