Mark E. Wood

University of Exeter

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Matthew Whiteman

University of Exeter

Alexis Perry

University of Exeter

Jack E. Baldwin

University of Manchester

Roberta Torregrossa

University of Exeter

Andrew M. Fryer

Array BioPharma (United States)

Matt Whiteman

University of Exeter

Jacqueline L. Whatmore

University of Exeter

Paul G. Winyard

University of Exeter

Csaba Szabó

University of Fribourg

Michael B. Hursthouse

University of Southampton

Cooperative Institutions

University of Exeter

100

University of Oxford

Western University

Universidade de São Paulo

London Health Sciences Centre

Dyson (United Kingdom)

National University of Singapore

Slovak Academy of Sciences

University of Debrecen

Imperial College London

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ChemInform Abstract: Towards a Versatile Synthesis of Kainoids. Part 3. Efficient Methods for Control of C‐4 Stereochemistry.

ChemInform (1997)

Jack E. Baldwin Andrew M. Fryer Mark R. Spyvee Roger C. Whitehead Mark E. Wood

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.199732164

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Mitochondria-targeted Hydrogen Sulfide (H 2 S), but not Untargeted H 2 S, Reverses Ventricular Arrhythmia at Reperfusion

Free Radical Biology and Medicine (2017)

Matthew Whiteman Qutuba G. Karwi Mark E. Wood Gary F. Baxter

10.1016/j.freeradbiomed.2017.10.189

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Citations (3)

Investigating the generation of hydrogen sulfide from the phosphonamidodithioate slow-release donor GYY4137

MedChemComm (2015)

Benjamin Alexander Simon J. Coles Bridget C. Fox Tahmina F. Khan Joseph Maliszewski

A two-step hydrolytic decomposition pathway has been elucidated for the slow-release hydrogen sulfide donor GYY4137.

10.1039/c5md00170f

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Citations (54)

CCDC 2291332: Experimental Crystal Structure Determination

The Cambridge Structural Database (2023)

Mark E. Wood Simon J. Coles Michael B. Hursthouse Steven J. Lamond

An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

10.5517/ccdc.csd.cc2gx9yn

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ChemInform Abstract: THE ADDITION TO 1,5‐DIMETHYL‐1‐V

Chemischer Informationsdienst (1977)

F. J. McQuillin Mark E. Wood

10.1002/chin.197725148

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ChemInform Abstract: A Stereocontrolled Synthesis of Protected (2R,3R)‐3‐Mercaptoaspartic Acid via a β‐Aspartyl Enolate Sulfenylation.

ChemInform (1996)

Norio Shibata Jack E. Baldwin Adam Jacobs Mark E. Wood

10.1002/chin.199642218

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Reaction of Alkyl Halides with Tin(II) Chloride in a Salt Melt

Compounds of Group 14 (Ge, Sn, Pb) (2003)

Mark E. Wood

10.1055/sos-sd-005-00268

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Fluoride/Chloride Exchange

Compounds of Group 14 (Ge, Sn, Pb) (2003)

Mark E. Wood

10.1055/sos-sd-005-00255

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A general route to protected quaternary α-amino acids from β-amino alcohols via a stereocontrolled radical approach

Chemical Communications (2006)

Mark E. Wood Mark J. Penny Jenny S. Steere Peter N. Horton Mark E. Light

A radical-based approach facilitates the highly stereocontrolled functionalisation of β-amino alcohols, opening up a new, generally applicable methodology for the preparation of quaternary α-amino acids.

Protein quaternary structure

10.1039/b604123j

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Citations (7)

PL04 Modulation of inflammatory and vascular signalling by novel slow release and mitochondria-targeted H2S donors

Nitric Oxide (2013)

Matthew Whiteman Alexis Perry Sophie Le Trionnaire Jacqueline L. Whatmore Tahanver Ahmed

Pathophysiology

10.1016/j.niox.2013.06.014

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Citations (1)