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Currently displaying 801 - 820 of 1025 publications

Dispiroketals in synthesis (part 6): Highly stereoselective alkylation of dispiroketal protected lactate and glycolate enolates

R Downham, KS Kim, SV Ley, M Woods

Tetrahedron Letters

(1994)

769

(doi: 10.1016/S0040-4039(00)75813-8)

DISPIROKETALS IN SYNTHESIS .5. A NEW OPPORTUNITY FOR OLIGOSACCHARIDE SYNTHESIS USING DIFFERENTIALLY ACTIVATED GLYCOSYL DONORS AND ACCEPTORS

G-J Boons, P Grice, R Leslie, SV Ley, LL Yeung

Tetrahedron Letters

(1993)

8523

(doi: 10.1016/S0040-4039(00)61375-8)

Selective Acylation and Alkylation Reactions of Diols Using Dibutyltin Dimethoxide

G-J Boons*, G Castle, J Clase, P Grice, S Ley, C Pinel

Synlett

(1993)

1993

913

(doi: 10.1055/s-1993-22650)

The chemistry of azadirachtin

SV Ley, AA Denholm, A Wood

Natural Product Reports

(1993)

109

(doi: 10.1039/np9931000109)

TOTAL SYNTHESIS OF THE SPIROKETAL MACROLIDE (+) MILBEMYCIN ALPHA(1)

SV Ley, A Madin, NJT Monck

Tetrahedron Letters

(1993)

7479

(doi: 10.1016/s0040-4039(00)60158-2)

Microwave Promoted Hydrolysis of Esters Absorbed on Alumina: A New Deprotection Method for Pivaloyl Groups

S Ley*, D Mynett

Synlett

(1993)

1993

793

(doi: 10.1055/s-1993-22612)

Synthesis of 4-substituted imidazoles via 4-metallo imidazole intermediates

R Turner*, S Ley, S Lindell

Synlett

(1993)

1993

748

(doi: 10.1055/s-1993-22594)

Dispiroketals in synthesis (part 4): Enantioselective desymmetrization of glycerol using a c2-symmetric disubstituted bis-dihydropyran.

B Geert-Jan, DA Entwistle, SV Ley, M Woods

Tetrahedron Letters

(1993)

5649

(doi: 10.1016/s0040-4039(00)73906-2)

CHEMISTRY OF INSECT ANTIFEEDANTS FROM AZADIRACHTA-INDICA .15. DEGRADATION STUDIES OF AZADIRACHTIN LEADING TO C8-C-14 BOND-CLEAVAGE

SV Ley, PJ Lovell, AMZ Slawin, SC Smith, DJ Williams, A Wood

Tetrahedron

(1993)

1675

(doi: 10.1016/s0040-4020(01)80354-9)

Some Alkylation and Reductive Amination Studies of b-Ketomacrolides as Potential Metal Speciation Materials

S V. Ley, S V. Kelkar

Heterocycles

(1993)

263

(doi: 10.3987/com-92-s12)

DISPIROKETALS IN SYNTHESIS .3. SELECTIVE PROTECTION OF DIEQUATORIAL VICINAL DIOLS IN CARBOHYDRATES

S Ley*, G-J Boons, R Leslie, M Woods, D Hollinshead

Synthesis

(1993)

1993

689

(doi: 10.1055/s-1993-25923)

UPTAKE, RETENTION, METABOLISM AND EXCRETION OF [22,23-H-3(2)]DIHYDROAZADIRACHTIN IN SCHISTOCERCA-GREGARIA

PA Paranagama, H Lovell, AA Denholm, SV Ley, JD Connolly, RHC Strang

Journal of Insect Physiology

(1993)

935

(doi: 10.1016/0022-1910(93)90003-a)

Microbial Oxidation in Synthesis: Preparation of a Potential Insulin Mimic from Benzene

S Ley*, L Yeung

Synlett

(1992)

1992

997

(doi: 10.1055/s-1992-21561)

Alfred bader [2]

SV Ley

Chemical and Engineering News

(1992)

CHEMISTRY OF INSECT ANTIFEEDANTS FROM AZADIRACHTA-INDICA .12. USE OF SILICON AS A CONTROL ELEMENT IN THE SYNTHESIS OF A HIGHLY FUNCTIONALIZED DECALIN FRAGMENT OF AZADIRACHTIN

HC Kolb, SV Ley, AMZ Slawin, DJ Williams

Journal of the Chemical Society Perkin Transactions 1

(1992)

2735

(doi: 10.1039/P19920002735)

Chemistry of insect antifeedants from Azadirachta indica, Part 14: Absolute configuration of azadirachtin

SV Ley, H Lovell, DJ Williams

Journal of the Chemical Society Chemical Communications

(1992)

1304

(doi: 10.1039/c39920001304)

Total synthesis of the ionophore antibiotic CP-61,405 (routiennocin)

D Díez-Martin, NR Kotecha, SV Ley, S Mantegani, JC Menéndez, HM Organ, AD White, BJ Banks

Tetrahedron

(1992)

7899

(doi: 10.1016/s0040-4020(01)80467-1)

DISPIROKETALS IN SYNTHESIS .2. A NEW GROUP FOR THE SELECTIVE PROTECTION OF DIEQUATORIAL VICINAL DIOLS IN CARBOHYDRATES

SV Ley, R Leslie, PD Tiffin, M Woods

Tetrahedron Letters

(1992)

4767

(doi: 10.1016/s0040-4039(00)61281-9)

BADER,ALFRED

SV LEY

CHEM ENG NEWS

(1992)

TOTAL SYNTHESIS OF THE CARBOXYLIC-ACID IONOPHORE ANTIBIOTIC CP-61,405 (ROUTIENNOCIN)

N Kotecha*, S Ley, S Mantegani

Synlett

(1992)

1992

395

(doi: 10.1055/s-1992-21357)

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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