Peter Hamley

AstraZeneca (United Kingdom)

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Alan C. Tinker

AstraZeneca (Brazil)

A.V. Wallace

Coventry University

Martin J. Bassindale

University of Strathclyde

Haydn G. Beaton

Loughborough University

AÅ

Anders Åberg

Karolinska Institutet

Stephen A. St-Gallay

AstraZeneca (United Kingdom)

David Nicholls

UK Centre for Ecology & Hydrology

Stephen Connolly

Newcastle upon Tyne Hospital

Andrew B. Holmes

University of South Dakota

David R. Cheshire

Loughborough University

Cooperative Institutions

Scripps Research Institute

AstraZeneca (United Kingdom)

Loughborough University

AstraZeneca (Sweden)

AstraZeneca (Brazil)

University of Cambridge

Philadelphia University

University of Pennsylvania

Merck & Co., Inc., Rahway, NJ, USA (United States)

Université Paris Cité

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Structure of murine iNOS oxygenase domain with inhibitor AR-C102222

Elsa D. Garcin A.S. Arvai R.J. Rosenfeld M.D. Kroeger Brian R. Crane

10.2210/pdb3e68/pdb

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Diastereoselective imino ester cycloadditions. Enantioselective synthesis of azabicyclo[2.2.1]heptenes

Journal of the Chemical Society Chemical Communications (1992)

Peter Hamley G�nter Helmchen Andrew B. Holmes David R. Marshall J. W. M. MACKINNON

The diethylaluminium chloride-catalysed cycloaddition of cyclopentadiene to the (S)-lactate-derived N-toluene-p-sulfonyliminoacetate 5 gives mainly (76% diastereoisomeric excess, d.e.) the adduct 9(X-ray structure); the (R)-pantolactone-derived iminoacetate 6 similarly gives (70% d.e.) the adduct 8 which is correlated via the methyl esters 11 with compound 9.

Cyclopentadiene

10.1039/c39920000786

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Citations (36)

Murine inos dimer with inhibitor 4-MAP bound

Elsa D. Garcin A.S. Arvai R.J. Rosenfeld M.D. Kroeger B.R. Crane

10.2210/pdb3e67/pdb

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Regio- and stereoselective functionalisation of monocyclic medium ring lactams

Tetrahedron Letters (1992)

P. Andrew Evans Ian Collins Peter Hamley Andrew B. Holmes Paul R. Raithby

Sodium azide

Staudinger reaction

10.1016/s0040-4039(00)61795-1

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Citations (14)

ChemInform Abstract: Thienopyridines: Nitric Oxide Synthase Inhibitors with Potent in vivo Activity.

ChemInform (2001)

Haydn G. Beaton N. K. Boughton-Smith Peter Hamley Anant Ghelani David Nicholls

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

10.1002/chin.200132150

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ChemInform Abstract: 3,4-Dihydro-1-isoquinolinamines: A Novel Class of Nitric Oxide Synthase Inhibitors with a Range of Isoform Selectivity and Potency.

ChemInform (2001)

Haydn G. Beaton Peter Hamley David Nicholls Alan C. Tinker A.V. Wallace

10.1002/chin.200132147

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The synthesis of angularly fused tricyclic compounds via tandem ring closing metathesis reactions

Chemical Communications (2000)

Martin J. Bassindale Andrew S. Edwards Harry Adams Joseph P. A. Harrity Peter Hamley

A novel and highly efficient approach to angularly fused tricycles has been developed through the employment of selective tandem ring closing metathesis reactions.

Tricyclic

Tandem

Ring-Closing Metathesis

Salt metathesis reaction

10.1039/b002136i

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Citations (22)

Spirocycle assembly through selective tandem ring closing metathesis reactions

Tetrahedron Letters (1999)

Martin J. Bassindale Peter Hamley Andreas Leitner Joseph P. A. Harrity

Tandem

Ring-Closing Metathesis