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Organic Letters|September 25, 2004
Self-condensation of N-tert-butanesulfinyl aldimines: application to the rapid asymmetric synthesis of biologically important amine-containing compoundsLaurie B Schenkel, Jonathan A EllmanOrganic Letters|February 14, 2003
Novel sulfinyl imine ligands for asymmetric catalysisLaurie B Schenkel, Jonathan A EllmanThe Journal of Organic Chemistry|April 3, 2004
Application of P,N-sulfinyl imine ligands to iridium-catalyzed asymmetric hydrogenation of olefinsLaurie B Schenkel, Jonathan A EllmanExperimental Hematology|January 24, 2013
Differential selectivity of JAK2 inhibitors in enzymatic and cellular settingsVioleta Yu, Jeanne Pistillo, Ivonne Archibeque, et al.Organic Letters|April 21, 2006
New air-stable catalysts for general and efficient suzuki-miyaura cross-coupling reactions of heteroaryl chloridesAnil S Guram, Anthony O King, John G Allen, et al.SLAS Discovery : Advancing Life Sciences R & D|December 20, 2019
Forced Self-Modification Assays as a Strategy to Screen MonoPARP EnzymesTim J Wigle, W David Church, Christina R Majer, et al.Bioorganic & Medicinal Chemistry Letters|June 24, 2014
Development of novel azabenzofuran TRPA1 antagonists as in vivo toolsKatrina W Copeland, Alessandro A Boezio, Eugene Cheung, et al.Immunohorizons|July 11, 2022
Selective Pharmaceutical Inhibition of PARP14 Mitigates Allergen-Induced IgE and Mucus Overproduction in a Mouse Model of Pulmonary Allergic ResponseAlex M Eddie, Kevin W Chen, Laurie B Schenkel, et al.The Journal of Organic Chemistry|March 31, 2012
Synthesis of 4-substituted chlorophthalazines, dihydrobenzoazepinediones, 2-pyrazolylbenzoic acid, and 2-pyrazolylbenzohydrazide via 3-substituted 3-hydroxyisoindolin-1-onesHanh Nho Nguyen, Victor J Cee, Holly L Deak, et al.Bioorganic & Medicinal Chemistry Letters|July 8, 2017
Discovery of a biarylamide series of potent, state-dependent NaV1.7 inhibitorsLaurie B Schenkel, Erin F DiMauro, Hanh N Nguyen, et al.Pageof 2