Publications

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Currently displaying 781 - 800 of 1071 publications

A General C-Glycosidation Procedure via Anomeric Oxygen to Carbon Rearrangements of Tetrahydropyranyl Ether Derivatives

M Buffet, D Dixon, G Edwards, S Ley*, E Tate

Synlett

(1997)

1997

1055

(doi: 10.1055/s-1997-1531)

One-Pot Synthesis of Tetra- and Pentasaccharides from Monomeric Building Blocks Using the Principles of Orthogonality and Reactivity Tuning

M-K Cheung, N Douglas, B Hinzen, S Ley*, X Pannecoucke

Synlett

(1997)

1997

257

(doi: 10.1055/s-1997-765)

Organic synthesis with tricarbonyliron lactone complexes

SV Ley

Philosophical Transactions of the Royal Society of London. Series A, Mathematical and Physical Sciences

(1997)

326

633

(doi: 10.1098/rsta.1988.0114)

Identification of Azadirachtin in Tissue-Cultured Cells of Neem (Azadirachta Indica)

AP Jarvis, ED Morgan, SA Van Der Esch, F Vitali, SV Ley, A Pape

Natural Product Letters

(1997)

(doi: 10.1080/10575639708043721)

Dispiroketals in synthesis .22. Use of chiral 2,2'-bis(phenylthiomethyl)dihydropyrans as new protecting and resolving agents for 1,2-diols (pg 791, 1996)

SV Ley, S Mio, B Meseguer

SYNLETT

(1996)

932

Direct protection of 1,2-diols from alpha-diketones (pg 793, 1996)

NL Douglas, SV Ley, HML Osborn, DR Owen, HWM Priepke, SL Warriner

SYNLETT

(1996)

932

Chemistry of insect antifeedants from Azadirachta indica .21. Synthesis of model compounds of azadirachtin using a decalin framework as a functional group scaffolding

ML de la Puente, SV Ley, MSJ Simmonds, WM Blaney

J CHEM SOC PERK T 1

(1996)

1523

(doi: 10.1039/p19960001523)

Chemistry of insect antifeedants from Azadirachta indica (part 20): synthesis of biologically active, simple analogues of azadirachtin, containing the hydroxytetrahydrofurancarboxylate hemiketal moiety

ML de la Puente, RB Grossman, SV Ley, MSJ Simmonds, WM Blaney

Journal of the Chemical Society Perkin Transactions 1

(1996)

1517

(doi: 10.1039/p19960001517)

Synthesis and chemistry of the ionophore antibiotic tetronasin.

SV Ley, JA Clase, DJ Mansfield

Farmaco

(1996)

147

(doi: 10.1002/jhet.5570330509)

(pi-Allyl)tricarbonyliron Lactone Complexes in Organic Synthesis: A Useful and Conceptually Unusual Route to Lactones and Lactams.

SV Ley, LR Cox, G Meek

Chem Rev

(1996)

423

(doi: 10.1021/cr950015t)

Diastereoselective addition reactions of allylstannanes to carbonyl groups in the side-chain of pi-allyltricarbonyliron lactone complexes

SV Ley, LR Cox

Chem. Commun.

(1996)

657

(doi: 10.1039/cc9960000657)

Autoradiographic localization of [22,23-H-3(2)] dihydroazadirachtin binding sites in desert locust testes and effects of Azadirachtin on sperm motility

AJ Nisbet, AJ Mordue Luntz, LM Williams, L Hannah, L Jennens, SV Ley, W Mordue

Tissue and Cell

(1996)

725

(doi: 10.1016/S0040-8166(96)80075-9)

Dispiroketals in Synthesis (Part 22)1: Use of Chiral 2,2′-Bis(phenylthiomethyl)-dihydropyrans as New Protecting and Resolving Agents for 1,2-Diols

S Ley*, S Mio, B Meseguer

Synlett

(1996)

1996

791

(doi: 10.1055/s-1996-5522)

Diastereoselective additions to aldehyde groups in the side-chain of π-allyltricarbonyliron lactone complexes

SV Ley, G Meek

Chemical Communications

(1996)

317

(doi: 10.1039/CC9960000317)

Dispiroketals in Synthesis (Part 20) 1: Preparation of Chiral 2,2′-Bis(halomethyl) and 2,2′-Bis(phenylthiomethyl)dihydropyrans

S Ley*, S Mio, B Meseguer

Synlett

(1996)

1996

787

(doi: 10.1055/s-1996-5520)

Direct Protection of 1,2-Diols from α-Diketones

N Douglas, S Ley*, H Osborn, D Owen, H Priepke, S Warriner

Synlett

(1996)

1996

793

(doi: 10.1055/s-1996-5523)

Synthetic studies towards the clerodane insect antifeedant jodrellin A: Preparation of a polycyclic model compound with antifeedant activity

AC Cuñat, D Díez-Martín, SV Ley, FJ Montgomery

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1

(1996)

611

(doi: 10.1039/P19960000611)

Dispiroketals in Synthesis (Part 21)1: Use of Chiral 2,2’-Bis(halomethyl)dihydropyrans as New Protecting and Resolving Agents for 1,2-Diols

S Ley*, S Mio

Synlett

(1996)

1996

789

(doi: 10.1055/s-1996-5521)

Dispiroketals: A new functional group for organic synthesis

SV Ley, R Downham, PJ Edwards, JE Innes, M Woods

Contemporary Organic Synthesis

(1995)

365

(doi: 10.1039/CO9950200365)

Spiroketal glycomimetics: the synthesis of a conformationally restrained Sialyl Lewis X mimic

AA Birkbeck, SV Ley, JC Prodger

Bioorganic & Medicinal Chemistry Letters

(1995)

2637

(doi: 10.1016/0960-894x(95)00469-a)

Papers of Interest

141. Preparation and use of tetra-n-propylammonium perruthenate (TPAP reagent) as new catalytic oxidants for alcohols J. Chem. Soc., Chem. Commun.,1987, 1625-1627.
659. The Synthesis of Azadirachtin Chem. Eur. J., 2008, 14, 10683-10704
366. Total synthesis of the protein phosphatase inhibitor okadaic acid J. Chem. Soc., Perkin Trans. 1, 1998, 3907-3912.
608. Total Synthesis of Rapamycin Angew. Chem., Int. Ed., 2007, 46, 591-597.
669. MultiStep Synthesis using Modular Flow Reactors Angew. Chem. Int. Ed., 2009, 48, 4017-4021
626. A Fascination with 1,2-Diacetals J. Org. Chem., 2007, 72, 5943-5959.
536. Multi-step Application of Immobilized Reagents and Scavengers: A Total Synthesis of Epothilone C Chem. Eur. J., 2004, 10, 2529-2547.
595. A Flow Process for the Multi-Step Synthesis of Oxomaritidine: A New Paradigm for Molecular Assembly J. Chem. Soc., Chem. Commun., 2006, 2566-2568.
785. Accelerating spirocyclic polyketide synthesis using flow chemistry Angew. Chem. Int. Edn., 2014, 53, 4915-4920
854. A Lewis Base Catalysis Approach for the Photoredox Activation of Boronic Acids and Esters Angew. Chem. Int. Ed., 2017, 56, 15136-15140

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