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Currently displaying 661 - 680 of 1024 publications

π-allyltricarbonyliron lactone complexes in a diastereoselective Mukaiyama aldol reaction.

SVJ Ley, EA Wright

ABSTR PAP AM CHEM S

(1999)

218

U51

Use of the Potassium Ion as a Template for the Selective Derivatization of the Antibiotic X-206

AC O'Sulliva, F Struber, SV Ley

The Journal of Organic Chemistry

(1999)

6252

(doi: 10.1021/jo9903151)

Synthesis of an array of potential matrix metalloproteinase inhibitors using a sequence of polymer-supported reagents

M Caldarelli, J Habermann, SV Ley

Bioorg Med Chem Lett

(1999)

2049

(doi: 10.1016/s0960-894x(99)00311-x)

Actions of azadirachtin, a plant allelochemical, against insects

AJ Mordue, MSJ Simmonds, SV Ley, WM Blaney, W Mordue, M Nasiruddin, AJ Nisbet

Pest Management Science

(1999)

277

(doi: 10.1002/(SICI)1096-9063(1998110)54:3<277::AID-PS801>3.0.CO;2-I)

Molybdenum(II)-Catalyzed Allylation of Electron-Rich Aromatics and Heteroaromatics

AV Malkov, SL Davis, IR Baxendale, WL Mitchell, P Kocovský

The Journal of organic chemistry

(1999)

2751

(doi: 10.1021/jo982178y)

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

AV Malkov, IR Baxendale, D Dvorák, DJ Mansfield, P Kocovský

The Journal of organic chemistry

(1999)

2737

(doi: 10.1021/jo9821776)

1,7-Induction of chirality in Mukaiyama aldol reactions using π-allyltricarbonyliron lactone and lactam complexes as chiral templates

SV Ley, LR Cox, B Middleton, JM Worrall

Tetrahedron

(1999)

3515

(doi: 10.1016/S0040-4020(98)01159-4)

Clean five-step synthesis of an array of 1,2,3,4-tetra-substituted pyrroles using polymer-supported reagents

M Caldarelli, J Habermann, SV Ley

Journal of the Chemical Society, Perkin Transactions 1

(1999)

107

(doi: 10.1039/a809345h)

Rapid assembly of oligosaccharides: Total synthesis of a glycosylphosphatidylinositol anchor of Trypanosoma brucei

DK Baeschlin, AR Chaperon, V Charbonneau, LG Green, SV Ley, U Lücking, E Walther

Angewandte Chemie International Edition

(1999)

3423

(doi: 10.1002/(sici)1521-3773(19981231)37:24<3423::aid-anie3423>3.0.co;2-i)

Prevalence of systemic hyprtension in morbid obesity.: Polysomnographic study.

M Fernández, V Rebollar, J Oseguera, A Orea, M Valencia, C Keirns, J Dorantes, M Reséndiz, M Rosales, R Campos, S Ley, X Gómez, J González-B, B García

HYPERTENSION

(1999)

1280

Chemical synthesis of the N-glycans of gp63, the major surface glycoprotein from Leishmania mexicana amazonensis

A Düffels, SV Ley

J CHEM SOC PERK T 1

(1999)

375

(doi: 10.1039/a809798d)

Polymer-supported hypervalent iodine reagents in ‘clean’ organic synthesis with potential application in combinatorial chemistry

SV Ley, AW Thomas, H Finch

J CHEM SOC PERK T 1

(1999)

669

(doi: 10.1039/a809799b)

Total synthesis of the polyenoyltetramic acid mycotoxin erythroskyrine†

DJ Dixon, SV Ley, T Gracza, P Szolcsanyi

Journal of the Chemical Society Perkin Transactions 1

(1999)

839

(doi: 10.1039/a809823i)

Dispiroketals in synthesis. Part 24. Preparation and use of chiral 2,2 '-bis(triisopropylsilyloxymethyl)bi(dihydropyran)s as new protecting and resolving agents for 1,2-diols

D Lainé, M Fujita, SV Ley

J CHEM SOC PERK T 1

(1999)

1639

(doi: 10.1039/a900950g)

Dispiroketals in synthesis. Part 25.1 Further reactions of dispiroketal protected glycolate to afford optically active 1,2,3,4-tetraols

M Fujita, D Lainé, SV Ley

Journal of the Chemical Society Perkin Transactions 1

(1999)

1647

(doi: 10.1039/a900951e)

Synthesis of the alkaloids (±)-oxomaritidine and (±)-epimaritidine using an orchestrated multi-step sequence of polymer supported reagents

SV Ley, O Schucht, AW Thomas, PJ Murray

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1

(1999)

1251

(doi: 10.1039/a901798d)

Synthesis of the potent analgesic compound (±)-epibatidine using an orchestrated multi-step sequence of polymer supported reagents

J Habermann, SV Ley, JS Scott

Journal of the Chemical Society Perkin Transactions 1

(1999)

1253

(doi: 10.1039/a901802f)

A general and efficient procedure for the preparation of enantiopure anti-1,2-diols -: synthesis and utility of (R′,R′,S,R)-2,3-butane diacetal protected butane tetrol

DJ Dixon, AC Foster, SV Ley, DJ Reynolds

Journal of the Chemical Society Perkin Transactions 1

(1999)

1635

(doi: 10.1039/a902732g)

Preparation of desymmetrised meso-tartrate derivatives -: synthesis and utility of (R′,R′,R,S)-2,3-butane diacetal protected dimethyl tartrate

DJ Dixon, AC Foster, SV Ley, DJ Reynolds

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1

(1999)

1631

(doi: 10.1039/a902733e)

New building blocks for efficient and highly diastereoselective polyol production-synthesis and utility of (R',R',S,S) and (S",S",R,R)-2,3-butane diacetal protected butane tetrol derivatives

JS Barlow, DJ Dixon, AC Foster, SV Ley, DJ Reynolds

Journal of the Chemical Society Perkin Transactions 1

(1999)

1627

(doi: 10.1039/a902734c)

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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About the Department

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Contact Professor Steven V. Ley Research Group

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Research at Cambridge