Yusuf Hamied Department of Chemistry

Publications by Professor Steve Ley CBE FRS FMedSci

A flow reactor process for the synthesis of peptides utilizing immobilized reagents, scavengers and catch and release protocols.
IR Baxendale, SV Ley, CD Smith, GK Tranmer
Chemical communications (Cambridge, England)
(2006)
(doi: 10.1039/b612197g)
A new asymmetric organocatalytic nitrocyclopropanation reaction
HM Hansen, DA Longbottom, SV Ley
Chem Commun (Camb)
(2006)
(doi: 10.1039/b612436b)
Sulphuration of Electron-Rich Arenes with Sulphenamides and Aminosulphenyl Chlorides
MU Bombala, SV Ley
Synthetic Communications
(2006)
10
(doi: 10.1080/00397918008062752)
Polymer-supported reagents and scavengers in synthesis
SV Ley, IR Baxendale, RM Myers
(2006)
3
Fully Automated Continuous Flow Synthesis of 4,5-Disubstituted Oxazoles
M Baumann, IR Baxendale, SV Ley, CD Smith, GK Tranmer
Organic Letters
(2006)
8
(doi: 10.1021/ol061975c)
Stereocontrolled total synthesis of bengazole a: a marine bisoxazole natural product displaying potent antifungal properties.
JA Bull, EP Balskus, RAJ Horan, M Langner, SV Ley
Angewandte Chemie International Edition
(2006)
45
(doi: 10.1002/anie.200602050)
An Enantioselective Organocatalytic Route to Chiral 3,6-Dihydropyridazines from Aldehydes
S Ley, A Oelke, S Kumarn, D Longbottom
Synlett
(2006)
2006
(doi: 10.1055/s-2006-951486)
ORGN 141-Asymmetric organocatalytic conjugate addition of malonates to enones using a proline tetrazole catalyst
KR Knudsen, CET Mitchell, S Brenner, SV Ley
ABSTR PAP AM CHEM S
(2006)
232
Enantioselective catalytic intramolecular cyclopropanation using modified cinchona alkaloid organocatalysts.
CCC Johansson, N Bremeyer, SV Ley, DR Owen, SC Smith, MJ Gaunt
Angewandte Chemie International Edition
(2006)
45
(doi: 10.1002/anie.200602129)
8,9,10,10a-Tetrahydro-6H-tetrazolo[1,5-a]pyrrolo[2,1-c]pyrazines: New Heterocyclic Frameworks Generated by an Ugi-Type Multicomponent Reaction
S Ley, V Franckevičius, D Longbottom, R Turner
Synthesis
(2006)
2006
(doi: 10.1055/s-2006-950219)
Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat 30NP.
SV Ley, AJP Stewart-Liddon, D Pears, RH Perni, K Treacher
Beilstein journal of organic chemistry
(2006)
2
(doi: 10.1186/1860-5397-2-15)
A highly selective, organocatalytic route to chiral 1,2-oxazines from ketones
S Kumarn, DM Shaw, SV Ley
Chemical Communications
(2006)
(doi: 10.1039/b606338a)
Natural Products as an Inspiration for the Discovery of New High-Throughput Chemical Synthesis Tools
SV Ley, IR Baxendale, DA Longbottom, RM Myers
(2006)
2
(doi: 10.1002/9780470085226.ch2)
Microwave-assisted Suzuki coupling reactions with an encapsulated palladium catalyst for batch and continuous-flow transformations
IR Baxendale, CM Griffiths-Jones, SV Ley, GK Tranmer
Chemistry - A European Journal
(2006)
12
(doi: 10.1002/chem.200501400)
The Use of Polymer Supported Reagents and Scavengers in the Synthesis of Natural Products
SV Ley, IR Baxendale, RM Myers
(2006)
(doi: 10.1201/9781420009279)
Effect of azadirachtin‐derived decalin (perhydronaphthalene) and dihydrofuranacetal (furo[2, 3‐fo]pyran) fragments on the feeding behaviour of Spodoptera littoralis
WM Blaney, MSJ Simmonds, SV Ley, JC Anderson, SC Smith, A Wood
Pesticide Science
(2006)
40
(doi: 10.1002/ps.2780400212)
Microwave flow chemistry: The next evolutionary step in synthetic chemistry?
IR Baxendale, MR Pitts
Chimica Oggi
(2006)
24
Progress towards avermectins and milbemycins
SV Ley
Pest Management Science
(2006)
18
(doi: 10.1002/ps.2780180210)
Targeting C-reactive protein for the treatment of cardiovascular disease.
MB Pepys, GM Hirschfield, GA Tennent, JR Gallimore, MC Kahan, V Bellotti, PN Hawkins, RM Myers, MD Smith, A Polara, AJA Cobb, SV Ley, JA Aquilina, CV Robinson, I Sharif, GA Gray, CA Sabin, MC Jenvey, SE Kolstoe, D Thompson, SP Wood
Nature
(2006)
440
(doi: 10.1038/nature04672)
Chemical variation of natural product-like scaffolds: Design and synthesis of spiroketal derivatives
G Zinzalla, L-G Milroy, SV Ley
Org Biomol Chem
(2006)
4
(doi: 10.1039/b603015g)
Yusuf Hamied Department of Chemistry
Lensfield Road
Cambridge
CB2 1EW
T: +44 (0) 1223 336300
enquiries@ch.cam.ac.uk
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