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Currently displaying 701 - 720 of 1024 publications

A new route to functionalised π-allyltricarbonyliron lactam complexes from aziridines and their use in stereoselective synthesis and oxidative conversion to β-lactams

SV Ley, B Middleton

Chemical Communications

(1998)

1995

(doi: 10.1039/a806236f)

Molybdenum(II)- and tungsten(II)-catalyzed allylic substitution

AV Malkov, IR Baxendale, DJ Mansfield, P Kocovsky

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY

(1998)

216

U548

Use of polymer supported reagents for clean multi-step organic synthesis: Preparation of amines and amine derivatives from alcohols for use in compound library generation

SV Ley, MH Bolli, B Hinzen, A-G Gervois, BJ Hall

Journal of the Chemical Society, Perkin Transactions 1

(1998)

2239

(doi: 10.1039/a803611j)

Synthesis of the acyltetronic acid ionophore tetronasin (ICI M139603)

SV Ley, DS Brown, JA Clase, AJ Fairbanks, IC Lennon, HMI Osborn, ESE StokeséOwen, DJ Wadsworth

Journal of the Chemical Society Perkin Transactions 1

(1998)

2259

(doi: 10.1039/a804170i)

Clean three-step synthesis of 4,5-dihydro-1H-pyrazoles starting from alcohols using polymer supported reagents

F Haunert, MH Bolli, B Hinzen, SV Ley

Journal of the Chemical Society, Perkin Transactions 1

(1998)

2235

(doi: 10.1039/a803609h)

Development of a polymer bound Wittig reaction and use in multi-step organic synthesis for the overall conversion of alcohols to beta-hydroxyamines

MH Bolli, SV Ley

J CHEM SOC PERK T 1

(1998)

2243

(doi: 10.1039/a803612h)

Stereoelectronic effects in the reactions of conformationally restricted, substituted cyclohexane-1,2-diones with 1,2-diols

R Lenz, SV Ley, DR Owen, SL Warriner

Tetrahedron Asymmetry

(1998)

2471

(doi: 10.1016/s0957-4166(98)00227-4)

Mukaiyama aldol reactions of π-allyltricarbonyliron lactone and lactam complexes bearing trimethylsilyl enol ether side-chains.: Not just formal, but genuine 1,7 induction of chirality

SV Ley, B Middleton, JM Worrall

Chemical Communications

(1998)

1339

(doi: 10.1039/a802878h)

Highly diasteroselective synthesis of β-hydroxy carbonyl compounds using π-allyltricarbonyliron lactone complexes:: a formal 1,7-asymmetric induction of chirality in a Mukaiyama aldol reaction (pg 227, 1998)

SV Ley, LR Cox

CHEMICAL COMMUNICATIONS

(1998)

851

A novel decomplexation of π-allyltricarbonyliron lactone complexes using borohydride reagents:: a new route to stereodefined acyclic 1,5-diols and 1,5,7-triols (pg 229, 1998)

SV Ley, S Burckhardt, LR Cox, JM Worrall

CHEMICAL COMMUNICATIONS

(1998)

851

A novel decomplexation of π-allyltricarbonyliron lactone complexes using borohydride reagents:: a new route to stereodefined acyclic 1,5-diols and 1,5,7-triols

SV Ley, JM Worrall

Chemical Communications

(1998)

229

(doi: 10.1039/a707155h)

Highly diastereoselective synthesis of β-hydroxy carbonyl compounds using π-allyltricarbonyliron lactone complexes: a formal 1,7-asymmetric induction of chirality in a Mukaiyama aldol reaction

SV Ley

Chemical Communications

(1998)

227

(doi: 10.1039/a707153a)

Tuning glycoside reactivity: New tool for efficient oligosaccharide synthesis

NL Douglas, SV Ley, U Lücking, SL Warriner

Journal of the Chemical Society, Perkin Transactions 1

(1998)

(doi: 10.1039/a705275h)

Synthesis of isoxazolidines using polymer supported perruthenate (PSP)

B Hinzen, SV Ley

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1

(1998)

(doi: 10.1039/a707340b)

Polymer Supported Perruthenate (PSP): Clean Oxidation of Primary Alcohols to Carbonyl Compounds Using Oxygen as Cooxidant

B Hinzen*

Synthesis

(1998)

1998

977

(doi: 10.1055/s-1998-2106)

Studies Towards the Synthesis of the C29-C51 Fragment of Altohyrtin A

E Fernandez-Megia*, N Gourlaouen, SV Ley, GJ Rowlands

Synlett

(1998)

1998

991

(doi: 10.1055/s-1998-3140)

Double diastereodifferentiation in the Mukaiyama aldol reactions of π-allyltricarbonyliron lactone complexes:: 1,7- vs. 1,2-asymmetric induction

SV Ley, LR Cox, JM Worrall

Journal of the Chemical Society, Perkin Transactions 1

(1998)

3349

(doi: 10.1039/a805996i)

Anomeric oxygen to carbon rearrangements of alkynyl tributylstannane derivatives of lactols

MF Buffet*, DJ Dixon, SV Ley, EW Tate

Synlett

(1998)

1998

1091

(doi: 10.1055/s-1998-1866)

One-pot synthesis of penta- and hepta-saccharides from monomeric mannose building blocks using the principles of orthogonality and reactivity tuning

L Green*, B Hinzen, SJ Ince, P Langer, SV Ley, SL Warriner

Synlett

(1998)

1998

440

(doi: 10.1055/s-1998-1659)

(1′S,2′S)-methyl-3O,4O-(1′,2′-dimethoxycyclohexane-1′,2′-diyl)-α-D-mannopyranoside [α-D-Mannopyranoside, methyl 3,4-O-(1,2-dimethoxy- 1,2-cyclohexanediyl)-, [3[S (S)]]-]

SV Ley, HMI Osborn, HWM Priepke, SL Warriner, KA Scheidt, WR Roush

Organic Syntheses

(1998)

170

(doi: 10.15227/orgsyn.075.0170)

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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Papers of Interest

About the Department

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Contact Professor Steven V. Ley Research Group

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Research at Cambridge