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Yusuf Hamied Department of Chemistry

 

Publications by Professor Steve Ley CBE FRS FMedSci

Generation of Reactive Ketenes under Flow Conditions through Zinc-Mediated Dehalogenation
A Hafner, SV Ley
– Synlett
(2015)
26,
1470
(DOI: 10.1055/s-0034-1380679)
A Versatile Room-Temperature Route to Di- and Trisubstituted Allenes Using Flow-Generated Diazo Compounds
JS Poh, DN Tran, C Battilocchio, JM Hawkins, SV Ley
– Angewandte Chemie - International Edition
(2015)
54,
7920
(DOI: 10.1002/anie.201501538)
Thiazole formation through a modified Gewald reaction
CJ Mallia, L Englert, GC Walter, IR Baxendale
– Beilstein J Org Chem
(2015)
11,
875
(DOI: 10.3762/bjoc.11.98)
Continuous Flow Metathesis for Direct Valorization of Food Waste: An Example of Cocoa Butter Triglyceride
C Schotten, D Plaza, S Manzini, SP Nolan, SV Ley, DL Browne, A Lapkin
– ACS sustainable chemistry & engineering
(2015)
3,
1453
(DOI: 10.1021/acssuschemeng.5b00397)
A Versatile Room-Temperature Route to Di- and Trisubstituted Allenes Using Flow-Generated Diazo Compounds.
J-S Poh, DN Tran, C Battilocchio, JM Hawkins, SV Ley
– Angew Chem Int Ed Engl
(2015)
54,
7920
(DOI: 10.1002/anie.201501538)
A Versatile Room‐Temperature Route to Di‐ and Trisubstituted Allenes Using Flow‐Generated Diazo Compounds
J Poh, DN Tran, C Battilocchio, JM Hawkins, SV Ley
– Angewandte Chemie
(2015)
127,
8031
(DOI: 10.1002/ange.201501538)
A practical deca-gram scale ring expansion of (<i>R</i>)-(-)-carvone to (<i>R</i>)-(+)-3-methyl-6-isopropenyl-cyclohept-3-enone-1
LDC Alves, AL Desiderá, KT de Oliveira, S Newton, SV Ley, TJ Brocksom
– Organic &amp; Biomolecular Chemistry
(2015)
13,
7633
(DOI: 10.1039/c5ob00525f)
Ethyl 2-hydroxy-2-phenyl-2-(thiazol-2-yl)acetate
CJ Mallia, L Englert, GC Walter, IR Baxendale
– Molbank
(2015)
2015,
M857
(DOI: 10.3390/M857)
Large-Scale Synthesis of Crystalline 1,2,3,4,6,7-Hexa-
C Stanetty, IR Baxendale
– European J Org Chem
(2015)
2015,
2718
(DOI: 10.1002/ejoc.201500024)
Flow synthesis of ethyl isocyanoacetate enabling the telescoped synthesis of 1,2,4-triazoles and pyrrolo-[1,2-c]pyrimidines.
M Baumann, AM Rodriguez Garcia, IR Baxendale
– Organic & biomolecular chemistry
(2015)
13,
4231
(DOI: 10.1039/c5ob00245a)
Syn-Ethyl 1-hydroxy-7-methoxy-2,3-dihydro-1H-pyrrolo[3,4-b]quinolone-3-carboxylate HCl Salt
M Baumann, IR Baxendale
– Molbank
(2015)
2015,
m846
(DOI: 10.3390/m846)
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)
Chemistry in a changing world
SV Ley, RM Myers, DE Fitzpatrick
– Actualite Chimique
(2015)
96
Flow Chemistry: Intelligent Processing of Gas-Liquid Transformations Using a Tube-in-Tube Reactor
M Brzozowski, M O'Brien, SV Ley, A Polyzos
– Acc Chem Res
(2015)
48,
349
(DOI: 10.1021/ar500359m)
Design, Synthesis, and Evaluation of Tetrasubstituted Pyridines as Potent 5-HT<sub>2C</sub> Receptor Agonists
G Rouquet, DE Moore, M Spain, DM Allwood, C Battilocchio, DC Blakemore, PV Fish, S Jenkinson, AS Jessiman, SV Ley, G McMurray, RI Storer
– ACS medicinal chemistry letters
(2015)
6,
329
(DOI: 10.1021/ml500507v)
Boehmeriasin A as new lead compound for the inhibition of topoisomerases and SIRT2
MS Christodoulou, F Calogero, M Baumann, AN García-Argáez, S Pieraccini, M Sironi, F Dapiaggi, R Bucci, G Broggini, S Gazzola, S Liekens, A Silvani, M Lahtela-Kakkonen, N Martinet, A Nonell-Canals, E Santamaría-Navarro, IR Baxendale, L Dalla Via, D Passarella
– European journal of medicinal chemistry
(2015)
92,
766
(DOI: 10.1016/j.ejmech.2015.01.038)
Organic synthesis: march of the machines.
SV Ley, DE Fitzpatrick, RJ Ingham, RM Myers
– Angew Chem Int Ed Engl
(2015)
54,
3449
(DOI: 10.1002/anie.201410744)
Development of a flow method for the hydroboration/oxidation of olefins.
JA Souto, RA Stockman, SV Ley
– Organic &amp; Biomolecular Chemistry
(2015)
13,
3871
(DOI: 10.1039/c5ob00170f)
Foreword
SV Ley
(2015)
2015-January,
vii
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
– Organic &amp; Biomolecular Chemistry
(2015)
13,
207
(DOI: 10.1039/c4ob02105c)

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