Professor Steven V. Ley Research Group

Publications

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  • Currently displaying 441 - 460 of 1049 publications
Author(s)
Publication title
Journal Name
Publication year
Foreword
P Nolan
(2006)
(doi: 10.1002/3527606858)
A highly enantioselective total synthesis of (+)-goniodiol
EW Tate, DJ Dixon, SV Ley
Org Biomol Chem
(2006)
4
(doi: 10.1039/b602805e)
A flow process for the multi-step synthesis of the alkaloid natural product oxomaritidine: a new paradigm for molecular assembly.
IR Baxendale, J Deeley, CM Griffiths-Jones, SV Ley, S Saaby, GK Tranmer
Chemical communications (Cambridge, England)
(2006)
(doi: 10.1039/b600382f)
Practical Synthesis of (S)-Pyrrolidin-2-yl-1H-tetrazole, Incorporating Efficient Protecting Group Removal by Flow-Reactor Hydrogenolysis
V Franckevicius, KR Knudsen, M Ladlow, DA Longbottom, SV Ley
Synlett
(2006)
2006
(doi: 10.1055/s-2006.939036)
Diastereoselective aldol reactions with butane-2,3-diacetal protected glyceraldehyde derivatives.
KR Knudsen, AF Stepan, P Michel, SV Ley
Organic and Biomolecular Chemistry
(2006)
4
(doi: 10.1039/b601888b)
Double conjugate addition of dithiols to propargylic carbonyl systems to generate protected 1,3-dicarbonyl compounds.
HF Sneddon, A van den Heuvel, AKH Hirsch, RA Booth, DM Shaw, MJ Gaunt, SV Ley
J Org Chem
(2006)
71
(doi: 10.1021/jo052514s)
Preparation of the neolignan natural product grossamide by a continuous-flow process
IR Baxendale, CM Griffiths-Jones, SV Ley, GK Tranmer
Synlett
(2006)
2006
(doi: 10.1055/S-2006-926244)
A New Strategy for Oligosaccharide Assembly Exploiting Cyclohexane‐1,2‐diacetal Methodology: An Efficient Synthesis of a High Mannose Type Nonasaccharide
P Grice, SV Ley, J Pietruszka, HMI Osborn, HWM Priepke, SL Warriner
Chemistry - A European Journal
(2006)
3
(doi: 10.1002/chem.19970030315)
Sexual development of malaria parasites is inhibited in vitro by the Neem extract Azadirachtin, and its semi-synthetic analogues
IW Jones, AA Denholm, SV Ley, H Lovell, A Wood, RE Sinden
FEMS Microbiol Lett
(2006)
120
(doi: 10.1111/j.1574-6968.1994.tb07044.x)
Diastereoselective aldol reactions with butane-2,3-diacetal protected glyceraldehyde derivatives (vol 4, pg 1471, 2006)
KR Knudsen, AF Stepan, P Michel, SV Ley
ORG BIOMOL CHEM
(2006)
4
Combinatorial Synthesis of Natural Product-Based Libraries
SV Ley, IR Baxendale, RM Myers
(2006)
(doi: 10.1201/9781420009279)
Asymmetric organocatalytic conjugate addition of malonates to enones using a proline tetrazole catalyst.
KR Knudsen, CET Mitchell, SV Ley
Chem. Commun.
(2005)
(doi: 10.1039/b514636d)
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives
SV Ley, DJ Dixon, RT Guy, F Rodríguez, TD Sheppard
Organic and Biomolecular Chemistry
(2005)
3
(doi: 10.1039/b512410g)
Evolution or Revolution: The Challenge to the Modern Medicinal Chemist
IR Baxendale, SV Ley
(2005)
Total Synthesis of Two Novel Subpicomolar Sarco/Endoplasmatic Reticulum Ca2+-ATPase Inhibitors Designed by an Analysis of the Binding Site of Thapsigargin
H Søhoel, T Liljefors, SV Ley, SF Oliver, A Antonello, MD Smith, CE Olsen, JT Isaacs, SB Christensen
Journal of Medicinal Chemistry
(2005)
48
(doi: 10.1021/jm058036v)
A versatile organocatalyst for the asymmetric conjugate addition of nitroalkanes to enones.
CET Mitchell, SE Brenner, SV Ley
Chemical communications (Cambridge, England)
(2005)
(doi: 10.1039/b511441a)
A Highly Selective, Organocatalytic Route to Chiral Dihydro-1,2-oxazines
S Kumarn, DM Shaw, DA Longbottom, SV Ley
Organic Letters
(2005)
7
(doi: 10.1021/ol051577u)
Total synthesis of Spongistatin 1: A synthetic strategy exploiting its latent pseudo-symmetry
M Ball, MJ Gaunt, DF Hook, AS Jessiman, S Kawahara, P Orsini, A Scolaro, AC Talbot, HR Tanner, S Yamanoi, SV Ley
Angewandte Chemie (International ed. in English)
(2005)
44
(doi: 10.1002/anie.200502008)
Synthesis of the EF Fragment of Spongistatin 1
S Kawahara, MJ Gaunt, A Scolaro, S Yamanoi, SV Ley
Synlett
(2005)
(doi: 10.1055/s-2005-871960)
Non-metal-catalysed intramolecular alkyne cyclotrimerization reactions promoted by focussed microwave heating in batch and flow modes
S Saaby, IR Baxendale, SV Ley
Organic & Biomolecular Chemistry
(2005)
3
(doi: 10.1039/b509540a)
Yusuf Hamied Department of Chemistry
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CB2 1EW
T: +44 (0) 1223 336300
enquiries@ch.cam.ac.uk
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