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  • Currently displaying 621 - 640 of 1021 publications
Author(s)
Publication title
Journal Name
Publication year
1,2-Diacetals: A New Opportunity for Organic Synthesis
SV Ley, DK Baeschlin, DJ Dixon, AC Foster, SJ Ince, HW Priepke, DJ Reynolds
Chemical Reviews
(2000)
101
A rapid approach for the optimisation of polymer supported reagents in synthesis
C Jamieson*, MS Congreve, DF Emiabata-Smith, SV Ley
Synlett
(2000)
2000
Multi-step organic synthesis using solid-supported reagents and scavengers: A new paradigm in chemical library generation
SV Ley, IR Baxendale, RN Bream, PS Jackson, AG Leach, DA Longbottom, M Nesi, JS Scott, RI Storer, SJ Taylor
Journal of the Chemical Society Perkin Transactions 1
(2000)
Oxygen to carbon rearrangements of anomerically linked alkenols from tetrahydropyran derivatives: An investigation of the reaction mechanism via a double isotopic labelling crossover study
MF Buffet, DJ Dixon, GL Edwards, SV Ley, EW Tate
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
(2000)
The synthesis of mono- and bicyclic ethers via acid catalysed ring-opening cyclisation of tetrahyclropyranyl ether derivatives
DJ Dixon, SV Ley, EW Tate
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
(2000)
Diastereoselective oxygen to carbon rearrangements of anomerically linked enol ethers and the total synthesis of (+)-(S,S )-(cis-6-methyltetrahydropyran-2-yl)acetic acid, a component of civet
DJ Dixon, SV Ley, EW Tate
J CHEM SOC PERK T 1
(2000)
The use of pi-allyltricarbonyliron lactone complexes in the synthesis of the resorcylic macrolides alpha- and beta-zearalenol
SV Ley, S Burckhardt
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
(2000)
Methyl 2,3-O-(6,6′-octahydro-6,6′-bi-2h-pyran-2,2′-diyl)-α-d- galactopyranoside: α-D-Galactopyranoside, methyl, 2,3-O-octahydro[2,2′-bi-2H-pyran]-2,2′-diyl-, [2(2R,2′R)-]
SV Ley, HMI Osborn
Organic Syntheses
(2000)
77
1,7-Asymmetric induction of chirality in a Mukaiyama aldol reaction using pi-allyltricarbonyliron lactone complexes: highly diastereoselective synthesis of alpha-substituted beta-hydroxy carbonyl compounds
SV Ley, EA Wright
J CHEM SOC PERK T 1
(2000)
A short stereoselective total synthesis of the fusarium toxin equisetin.
LT Burke, DJ Dixon, SV Ley, F Rodríguez
Org Lett
(2000)
2
The total synthesis of the annonaceous acetogenin, muricatetrocin C
DJ Dixon, SV Ley, DJ Reynolds
Angewandte Chemie International Edition
(2000)
39
The Total Synthesis of the Annonaceous Acetogenin, Muricatetrocin C
DJ Dixon, SV Ley, DJ Reynolds
Angew Chem Int Ed Engl
(2000)
39
Chemoenzymatic synthesis of L-galactosylated dimeric sialyl Lewis X structures employing α-1,3-fucosyltransferase V
A Düffels, LG Green, R Lenz, SV Ley, SP Vincent, CH Wong
Bioorganic and Medicinal Chemistry
(2000)
8
Polymer-supported reagents for multi-step organic synthesis: Application to the synthesis of sildenafil
IR Baxendale, SV Ley
Bioorganic & Medicinal Chemistry Letters
(2000)
10
Combined application of analytical techniques for the characterization of polymer supported species
P Grice, AG Leach, SV Ley, A Massi, DM Mynett
ACS Combinatorial Science
(2000)
2
Chemo-enzymatic synthesis of fluorinated sugar nucleotide: Useful mechanistic probes for glycosyltransferases
MD Burkart, SP Vincent, A Düffels, BW Murray, SV Ley, CH Wong
Bioorganic & medicinal chemistry
(2000)
8
Protecting groups: Effects on reactivity, glycosylation stereoselectivity, and coupling efficiency
LG Green, SV Ley, B Ernst, GW Hart, P Sinaý
(2000)
1-4
Synthesis of High‐Mannose Type Neoglycolipids: Active Targeting of Liposomes to Macrophages in Gene Therapy
A Düffels, LG Green, SV Ley, AD Miller
Chemistry (Weinheim an der Bergstrasse, Germany)
(2000)
6
Pinene-derived bipyridine ligands (PINDY) in asymmetric catalysis.
AV Malkov, IR Baxendale, M Bella, V Langer, P Kocovsky
ABSTR PAP AM CHEM S
(2000)
219
Polymer Supported Reagents in Synthesis: Preparation of Bicyclo[2.2.2]octane Derivatives via Tandem Michael Addition Reactions and Subsequent Combinatorial Decoration
SV Ley, A Massi
ACS Combinatorial Science
(2000)
2

Papers of Interest