研究领域
Synthesis/Biological/Materials
In the Ley Group, we specialise in developing new synthesis methods and applying them to the construction of biologically important molecules. Over the last 4 years we have completed the total synthesis of 38 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 140 completed total syntheses. In addition to our research on natural product synthesis, we have the Innovative Technology Centre (ITC); a new state-of-the-art flow chemistry facility. Our group is also part of the Cambridge PhD Training Programme in Chemical Biology and Molecular Medicine.
近期论文
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Development of a flow method for the hydroboration/oxidation of olefins.
JA Souto, RA Stockman, SV Ley – Org Biomol Chem (2015)
(DOI: 10.1039/c5ob00170f)
Back pressure regulation of slurry-forming reactions in continuous flow
BJ Deadman, DL Browne, IR Baxendale, SV Ley – Chemical Engineering and Technology (2015) 38, 259
(DOI: 10.1002/ceat.201400445)
Flow chemistry as a discovery tool to access sp2-sp3 cross-coupling reactions via diazo compounds
DN Tran, C Battilocchio, S-B Lou, JM Hawkins, SV Ley – Chem. Sci. (2015) 6, 1120
(DOI: 10.1039/C4SC03072A)
Flow chemistry: Intelligent processing of gas-liquid transformations using a tube-in-tube reactor
M Brzozowski, M O'Brien, SV Ley, A Polyzos – Accounts of Chemical Research (2015) 48, 349
(DOI: 10.1021/ar500359m)
Cyclopropanation using flow-generated diazo compounds.
NM Roda, DN Tran, C Battilocchio, R Labes, RJ Ingham, JM Hawkins, SV Ley – Org Biomol Chem (2015) 13, 2550
(DOI: 10.1039/c5ob00019j)
Organic Synthesis: March of the Machines.
SV Ley, DE Fitzpatrick, RJ Ingham, RM Myers – Angew Chem Int Ed Engl (2015) 54, n/a
(DOI: 10.1002/anie.201410744)
Back Pressure Regulation of Slurry-Forming Reactions in Continuous Flow
BJ Deadman, DL Browne, IR Baxendale, SV Ley – Chemical Engineering and Technology (2015) 38, 259
(DOI: 10.1002/ceat.201400445)
Total syntheses of linear polythiazole/oxazole plantazolicin A and its biosynthetic precursor plantazolicin B
ZE Wilson, S Fenner, SV Ley – Angew Chem Int Ed Engl (2015) 54, 1284
(DOI: 10.1002/anie.201410063)
Process intensification for the continuous flow hydrogenation of ethyl nicotinate
T Ouchi, C Battilocchio, JM Hawkins, SV Ley – Organic Process Research and Development (2014) 18, 1560
(DOI: 10.1021/op500208j)
A Systems Approach towards an Intelligent and Self-Controlling Platform for Integrated Continuous Reaction Sequences
RJ Ingham, C Battilocchio, DE Fitzpatrick, E Sliwinski, JM Hawkins, SV Ley – Angew Chem Int Ed Engl (2015) 54, 144
(DOI: 10.1002/anie.201409356)
The rapid synthesis of oxazolines and their heterogeneous oxidation to oxazoles under flow conditions
S Glöckner, DN Tran, RJ Ingham, S Fenner, ZE Wilson, C Battilocchio, SV Ley – Org Biomol Chem (2015) 13, 207
(DOI: 10.1039/c4ob02105c)
Design and application of a low-temperature continuous flow chemistry platform
JA Newby, DW Blaylock, PM Witt, JC Pastre, MK Zacharova, SV Ley, DL Browne – Organic Process Research and Development (2014) 18, 1211
(DOI: 10.1021/op500213j)
Reconfiguration of a continuous flow platform for extended operation: Application to a cryogenic fluorine-directed ortho-lithiation reaction
JA Newby, DW Blaylock, PM Witt, RM Turner, PL Heider, BH Harji, DL Browne, SV Ley – Organic Process Research and Development (2014) 18, 1221
(DOI: 10.1021/op500221s)
A general continuous flow method for palladium catalysed carbonylation reactions using single and multiple tube-in-tube gas-liquid microreactors
U Gross, P Koos, M O'Brien, A Polyzos, SV Ley – European Journal of Organic Chemistry (2014) 2014, 6418
(DOI: 10.1002/ejoc.201402804)
Flow chemistry meets advanced functional materials.
RM Myers, DE Fitzpatrick, RM Turner, SV Ley – Chemistry (2014) 20, 12348
(DOI: 10.1002/chem.201402801)
Expedient preparation of nazlinine and a small library of indole alkaloids using flow electrochemistry as an enabling technology
MA Kabeshov, B Musio, PR Murray, DL Browne, SV Ley – Organic Letters (2014) 16, 4618
(DOI: 10.1021/ol502201d)
Regioselective preparation of saturated spirocyclic and ring-expanded fused pyrazoles
RR Merchant, DM Allwood, DC Blakemore, SV Ley – J Org Chem (2014) 79, 8800
(DOI: 10.1021/jo501624t)
Highly regioselective lithiation of pyridines bearing an oxetane unit by n-butyllithium
G Rouquet, DC Blakemore, SV Ley – Chemical communications (Cambridge, England) (2014) 50, 8908
(DOI: 10.1039/C4CC03766A)
Preparation of unsymmetrical ketones from tosylhydrazones and aromatic aldehydes via formyl C-H bond insertion.
DM Allwood, DC Blakemore, SV Ley – Organic Letters (2014) 16, 3064
(DOI: 10.1021/ol5011714)
Continuous flow chemistry: a discovery tool for new chemical reactivity patterns.
J Hartwig, JB Metternich, N Nikbin, A Kirschning, SV Ley – Org Biomol Chem (2014) 12, 3611
(DOI: 10.1039/c4ob00662c)