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Jonathan M Large

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Combinatorial Chemistry & High Throughput Screening|March 12, 2009
Design and combinatorial synthesis of a library of methylenesulfonamides and related compounds as potential kinase inhibitorsJane E Torr, Jonathan M Large, Edward McDonald
Organic Letters|January 31, 2022
Diarylamine Synthesis via Desulfinylative Smiles RearrangementThomas Sephton, Jonathan M Large, Sam Butterworth, et al.
Organic Letters|September 5, 2023
Synthesis of Functionalized Pyrrolidinone Scaffolds via Smiles-Truce CascadeThomas Sephton, Jonathan M Large, Sam Butterworth, et al.
Structure (London, England : 1993)|May 14, 2013
Structure of rhomboid protease in complex with β-lactam inhibitors defines the S2' cavityKutti R Vinothkumar, Olivier A Pierrat, Jonathan M Large, et al.
Frontiers in Molecular Neuroscience|April 30, 2024
Targeted protein degradation in CNS disorders: a promising route to novel therapeutics?Sandra Kuemper, Andrew G Cairns, Kristian Birchall, et al.
Angewandte Chemie (International Ed. in English)|May 31, 2024
XAT-Catalysis for Intramolecular Biaryl SynthesisThomas Sephton, Jonathan M Large, Louise S Natrajan, et al.
Frontiers in Microbiology|January 4, 2021
Targeting the Malaria Parasite cGMP-Dependent Protein Kinase to Develop New DrugsDavid A Baker, Alexios N Matralis, Simon A Osborne, et al.
Angewandte Chemie (International Ed. in English)|October 18, 2023
Aryne-Enabled C-N Arylation of AnilinesThomas Sephton, Anastasios Charitou, Cristina Trujillo, et al.
Bioorganic & Medicinal Chemistry Letters|November 13, 2003
Synthesis and nicotinic binding of novel phenyl derivatives of UB-165. Identifying factors associated with alpha7 selectivityGunter Karig, Jonathan M Large, Christopher G V Sharples, et al.
SLAS Discovery : Advancing Life Sciences R & D|December 30, 2020
A "Target Class" Screen to Identify Activators of Two-Pore Domain Potassium (K2P) ChannelsDavid McCoull, Emma Ococks, Jonathan M Large, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Combinatorial Chemistry & High Throughput Screening|March 12, 2009
Design and combinatorial synthesis of a library of methylenesulfonamides and related compounds as potential kinase inhibitorsJane E Torr, Jonathan M Large, Edward McDonald
Organic Letters|January 31, 2022
Diarylamine Synthesis via Desulfinylative Smiles RearrangementThomas Sephton, Jonathan M Large, Sam Butterworth, et al.
Organic Letters|September 5, 2023
Synthesis of Functionalized Pyrrolidinone Scaffolds via Smiles-Truce CascadeThomas Sephton, Jonathan M Large, Sam Butterworth, et al.
Structure (London, England : 1993)|May 14, 2013
Structure of rhomboid protease in complex with β-lactam inhibitors defines the S2' cavityKutti R Vinothkumar, Olivier A Pierrat, Jonathan M Large, et al.
Frontiers in Molecular Neuroscience|April 30, 2024
Targeted protein degradation in CNS disorders: a promising route to novel therapeutics?Sandra Kuemper, Andrew G Cairns, Kristian Birchall, et al.
Angewandte Chemie (International Ed. in English)|May 31, 2024
XAT-Catalysis for Intramolecular Biaryl SynthesisThomas Sephton, Jonathan M Large, Louise S Natrajan, et al.
Frontiers in Microbiology|January 4, 2021
Targeting the Malaria Parasite cGMP-Dependent Protein Kinase to Develop New DrugsDavid A Baker, Alexios N Matralis, Simon A Osborne, et al.
Angewandte Chemie (International Ed. in English)|October 18, 2023
Aryne-Enabled C-N Arylation of AnilinesThomas Sephton, Anastasios Charitou, Cristina Trujillo, et al.
Bioorganic & Medicinal Chemistry Letters|November 13, 2003
Synthesis and nicotinic binding of novel phenyl derivatives of UB-165. Identifying factors associated with alpha7 selectivityGunter Karig, Jonathan M Large, Christopher G V Sharples, et al.
SLAS Discovery : Advancing Life Sciences R & D|December 30, 2020
A "Target Class" Screen to Identify Activators of Two-Pore Domain Potassium (K2P) ChannelsDavid McCoull, Emma Ococks, Jonathan M Large, et al.
Pageof 3