D. Fengas

The discovery and optimization of benzimidazoles as selective NaV1.8 blockers for the treatment of pain.

A. Brown, E. Stevens, J. Warmus, 2019, Bioorganic & medicinal chemistry.

Bifurcate, tandem ATRC reactions: Towards 2-oxabicyclo[4.3.0]nonane core of eunicellins

J. Raftery, M. Helliwell, P. Quayle, 2005 .

A Practical Synthesis of 3,3‐Difluorocyclobutane Carboxylic Acid

M. Fray, D. Fengas, Dirk L. Elend, 2005 .

Toward catalyst economy : A programmed approach to the synthesis of bicyclic lactones and lactams

J. Raftery, Chris D. Edlin, D. House, 2006 .

Atom Transfer Radical Cyclisations Mediated by the Grubbs Ruthenium Metathesis Catalyst

P. Quayle, S. Richards, D. Fengas, 2003 .

Practical Synthesis of (1s,4s)-4-(Methylamino)-1′H-spiro[cyclohexane-1,3′-furo[3,4-c]pyridin]-1′-one

G. Bish, M. Fray, Stephané P. A. Dubant, 2010 .

Identification of substance P metabolites using a combination of reversed-phase high-performance liquid chromatography and capillary electrophoresis.

R. Whelpton, A. Michael-Titus, S. Stephens, 1998, Journal of chromatography. B, Biomedical sciences and applications.

Intramolecular metathesis versus Kharasch reactions using the Grubbs metathesis catalyst: towards catalyst economy

Chris D. Edlin, P. Quayle, S. Richards, 2005 .

Discovery of Allosteric, Potent, Subtype Selective, and Peripherally Restricted TrkA Kinase Inhibitors.

R. Grimley, J. Bilsland, J. Cui, 2019, Journal of medicinal chemistry.

Highly potent and selective NaV1.7 inhibitors for use as intravenous agents and chemical probes.

Brian E Marron, Neil A Castle, Rubben Torella, 2017, Bioorganic & medicinal chemistry letters.