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Journal of Medicinal Chemistry|July 15, 2020
The Most Common Functional Groups in Bioactive Molecules and How Their Popularity Has Evolved over TimePeter Ertl, Eva Altmann, Jeffrey M McKennaOrganic Letters|December 24, 2014
Amine protection/α-activation with the tert-butoxythiocarbonyl group: application to azetidine lithiation-electrophilic substitutionDavid M Hodgson, Claire L Mortimer, Jeffrey M McKennaAdvanced Synthesis & Catalysis|May 20, 2014
Gold Catalysed Redox Synthesis of Imidazo[1,2-<i>a</i>]pyridine using Pyridine <i>N</i>-Oxide and AlkynesEric P A Talbot, Melodie Richardson, Jeffrey M McKenna, et al.Journal of the American Chemical Society|June 26, 2018
Chiral Diaryliodonium Phosphate Enables Light Driven Diastereoselective α-C(sp<sup>3</sup>)-H AcetalizationBaihua Ye, Jie Zhao, Ke Zhao, et al.Journal of the American Chemical Society|March 13, 2014
Asymmetric palladium-catalyzed directed intermolecular fluoroarylation of styrenesEric P A Talbot, Talita de A Fernandes, Jeffrey M McKenna, et al.Journal of Chromatography. A|February 1, 2025
A 'One-Shot' strategy for preparative chiral sub/supercritical fluid chromatography with chiroptical detection accelerates purification and enhances characterization for drug discoveryJohn Reilly, Marie-Anne Lozach, Aldo Meishammer, et al.ACS Chemical Biology|March 20, 2023
Targeted Protein Degradation through E2 RecruitmentNafsika Forte, Dustin Dovala, Matthew J Hesse, et al.Cell Chemical Biology|March 10, 2023
Chemoproteomics-enabled discovery of a covalent molecular glue degrader targeting NF-κBElizabeth A King, Yoojin Cho, Nathan S Hsu, et al.The Journal of Organic Chemistry|September 25, 2015
α- and α'-Lithiation-Electrophile Trapping of N-Thiopivaloyl and N-tert-Butoxythiocarbonyl α-Substituted Azetidines: Rationalization of the Regiodivergence Using NMR and ComputationKelvin E Jackson, Claire L Mortimer, Barbara Odell, et al.Journal of Medicinal Chemistry|May 17, 2002
An algorithm-directed two-component library synthesized via solid-phase methodology yielding potent and orally bioavailable p38 MAP kinase inhibitorsJeffrey M McKenna, Frank Halley, John E Souness, et al.Pageof 4