Professor Steven V. Ley Research Group

Publications

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  • Currently displaying 781 - 800 of 1049 publications
Author(s)
Publication title
Journal Name
Publication year
Behavioural and neurophysiological responses of Spodoptera littoralis to azadirachtin and a range of synthetic analogues.
MSJ Simmonds, WM Blaney, SV Ley, JC Anderson, R Banteli, AA Denholm, PCW Green, RB Grossman, C Gutteridge, L Jennens
Entomologia Experimentalis et Applicata.
(1995)
77
(doi: 10.1111/j.1570-7458.1995.tb01987.x)
Dispiroketals in synthesis (part 19)1: Dispiroketals as enantioselective and regioselective protective agents for symmetric cyclic and acyclic polyols.
R DOWNHAM, PJ EDWARDS, DA ENTWISTLE, AB HUGHES, KS KIM, SV LEY
Tetrahedron: Asymmetry
(1995)
6
(doi: 10.1016/0957-4166(95)00318-j)
Dispiroketals in Synthesis (Part 18)1: Regioselective and Enantioselective Protection of Symmetric Polyol Substrates Using an Enantiopure (2S,2’S)-Dimethyl-bis-dihydropyran
PJ EDWARDS, SV LEY
Synlett
(1995)
1995
(doi: 10.1055/s-1995-5122)
SYNTHESIS AND CHEMISTRY OF THE INSECT ANTIFEEDANT AZADIRACHTIN
SV LEY
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(1995)
210
Regiospecific fragmentation of benzene derivatives: synthetic and analytical applications
NJ HALES, H HEANEY, JH HOLLINSHEAD, SV LEY
Tetrahedron
(1995)
51
(doi: 10.1016/0040-4020(95)00395-o)
The synthesis and assay of radiolabelled benzene derivatives
NJ HALES, H HEANEY, JH HOLLINSHEAD, SV LEY
Tetrahedron
(1995)
51
(doi: 10.1016/0040-4020(95)00394-n)
CYCLOHEXANE-1,2-DIACETALS IN SYNTHESIS .3. TUNING THE REACTIVITY OF GLYCOSIDES - EFFICIENT ONE-POT OLIGOSACCHARIDE SYNTHESIS
P GRICE, SV LEY, J PIETRUSZKA, HWM PRIEPKE, EPE WALTHER
SYNLETT
(1995)
Tuning the reactivity of glycosides: Efficient one-pot oligosaccharide synthesis
P Grice, SV Ley, J Pietruszka, HWM Priepke, EPE Walther
Synlett
(1995)
1995
(doi: 10.1055/s-1995-5052)
Chemistry of insect antifeedants from Azadirachta Indica (Part 19): 1A potential relay route for the synthesis of azadirachtin
AA DENHOLM, L JENNENS, SV LEY, A WOOD
Tetrahedron
(1995)
51
(doi: 10.1016/0040-4020(95)00297-l)
Biosynthesis of tetronasin: Part 4, preparation of deuterium labelled C19-C26, C17-C26, C11-C26 and C3-C26 polyketide fragments as putative biosynthetic precursors of the ionophore antibiotic tetronasin (ICI 139603)
GJ BOONS, JA CLASE, IC LENNON, SV LEY, J STAUNTON
Tetrahedron
(1995)
51
(doi: 10.1016/0040-4020(95)00201-i)
CHEMISTRY OF INSECT ANTIFEEDANTS FROM AZADIRACHTA-INDICA .18. DEMETHYLATION AND METHYLATION OF THE C-8 POSITION OF THE DECALIN PORTION OF AZADIRACHTIN
WJ KOOT, SV LEY
Tetrahedron
(1995)
51
(doi: 10.1016/0040-4020(94)01071-7)
Synthesis of β-dimorphecolic acid exploiting highly stereoselective reduction of a side-chain carbonyl group in a π-allyltricarbonyliron lactone complex
SV LEY, G MEEK
Journal of the Chemical Society Chemical Communications
(1995)
(doi: 10.1039/c39950001751)
Dispiroketals in synthesis (part 19)1: Dispiroketals as enantioselective and regioselective protective agents for symmetric cyclic and acyclic polyols.
R Downham, PJ Edwards, DA Entwistle, AB Hughes, KS Kim, SV Ley
Tetrahedron Asymmetry
(1995)
6
(doi: 10.1016/0957-4166(95)00318-J)
Behavioural responses of locusts and Spodoptera littoralis to azadirachtin and azadirachtin analogues containing fluorescent and immunogenic reporter groups
MSJ SIMMONDS, WM BLANEY, RB GROSSMAN, SV LEY
Journal of Insect Physiology
(1995)
41
(doi: 10.1016/0022-1910(95)00014-l)
"Connectivist" approach to organic structure determination Lsd-program assisted Nmr analysis of the insect antifeedant Azadirachtin
SV LEY, K DOHERTY, G MASSIOT, JM NUZILLARD
Tetrahedron
(1994)
50
(doi: 10.1016/S0040-4020(01)89576-4)
Dispiroketals in synthesis (Part 13): Functionalised dispiroketals as new chiral auxiliaries; highly stereoselective diels-alder reactions using a bifunctional, C2- symmetrical chiral auxiliary
BCB BEZUIDENHOUDT, GH CASTLE, JV GEDEN, SV LEY
Tetrahedron Letters
(1994)
35
(doi: 10.1016/0040-4039(94)85339-8)
Dispiroketals in synthesis (Part 12): Functionalised dispiroketals as new chiral auxiliaries; the synthesis of dihydroxylated dispiroketals in optically pure form
BCB BEZUIDENHOUDT, GH CASTLE, SV LEY
Tetrahedron Letters
(1994)
35
(doi: 10.1016/0040-4039(94)85338-X)
Dispiroketals in synthesis (Part 11): Concomitant enantioselective and regioselective protection of 2,5- dibenzoyl-myo-inositol
PJ Edwards, DA Entwistle, C Genicot, KS Kim, SV Ley
Tetrahedron Letters
(1994)
35
(doi: 10.1016/0040-4039(94)85337-1)
Dispiroketals in synthesis (Part 11): Concomitant enantioselective and regioselective protection of 2,5- dibenzoyl-myo-inositol
PJ EDWARDS, DA ENTWISTLE, C GENICOT, KS KIM, SV LEY
Tetrahedron Letters
(1994)
35
(doi: 10.1016/0040-4039(94)85337-1)
Dispiroketals in synthesis (Part 14): Functionalised dispiroketals as new chiral auxiliaries; highly stereoselective Michael additions to a bifunctional, C2- symmetrical chiral auxiliary
GH CASTLE, SV LEY
Tetrahedron Letters
(1994)
35
(doi: 10.1016/0040-4039(94)85340-1)
Yusuf Hamied Department of Chemistry
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