L. McMurray

发表

Recent developments in natural product synthesis using metal-catalysed C-H bond functionalisation.

M. Gaunt, F. O’Hara, L. McMurray, 2011, Chemical Society reviews.

A unified “top-down” approach for the synthesis of diverse lead-like molecular scaffolds

S. Marsden, A. Nelson, L. McMurray, 2022, Bioorganic & Medicinal Chemistry Letters.

Identification and Strategies to Mitigate High Total Clearance of Benzylamine-Substituted Biphenyl Ring Systems.

B. Williamson, Aixiang Xue, S. Boyd, 2022, Molecular pharmaceutics.

Recent Advances in Photocatalytic Decarboxylative Coupling Reactions in Medicinal Chemistry

T. McGuire, R. Howells, L. McMurray, 2020, Synthesis.

Pharmacological inhibition of MERTK induces in vivo retinal degeneration: a multimodal imaging ocular safety assessment

M. Coen, A. Doherty, G. Maglennon, 2022, Archives of toxicology.

Copper-catalyzed alkene arylation with diaryliodonium salts.

Robert J. Phipps, M. Gaunt, L. McMurray, 2012, Journal of the American Chemical Society.

Chemical synthesis of Aspidosperma alkaloids inspired by the reverse of the biosynthesis of the rhazinilam family of natural products.

M. Gaunt, E. M. Beck, L. McMurray, 2012, Angewandte Chemie.

Generating Selective Leads for Mer Kinase Inhibitors-Example of a Comprehensive Lead-Generation Strategy.

Anthony D. Keefe, E. Hennessy, A. Keefe, 2021, Journal of medicinal chemistry.

Discovery of a Potent and Orally Bioavailable Zwitterionic Series of Selective Estrogen Receptor Degrader-Antagonists.

J. Breed, J. Nissink, Paul R. J. Davey, 2023, Journal of medicinal chemistry.

Optimization of an Imidazo[1,2-a]pyridine Series to Afford Highly Selective Type I1/2 Dual Mer/Axl Kinase Inhibitors with In Vivo Efficacy.

E. Hennessy, Nichola L. Davies, A. Doherty, 2021, Journal of medicinal chemistry.