Stephen L. Buchwald
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Read more: Enantioselective β-arylation of ketones enabled by lithiation/borylation/1,4-addition sequence under flow conditionsShu, W.Buchwald, S. L.
Enantioselective β-arylation of ketones enabled by lithiation/borylation/1,4-addition sequence under flow conditions
Angew. Chem. Int. Ed.,2012,515355-5358. -
Read more: Engaging Aldehydes in CuH-Catalyzed Reductive Coupling Reactions: Stereoselective Allylation with Unactivated 1,3-Diene PronucleophilesChengxi Li*Kwangmin Shin*Richard Y.LiuStephen L. Buchwald
Engaging Aldehydes in CuH-Catalyzed Reductive Coupling Reactions: Stereoselective Allylation with Unactivated 1,3-Diene Pronucleophiles
Angew. Chem. Int. Ed.,2019,5817074-17080. -
Read more: Engineering Bioactive Dimeric Transcription Factor Analogs via Palladium Rebound ReagentsMuhammad JbaraSebastian PomplunCarly K. SchisselSusana Wilson HawkenAnn BoijaIsaac KleinJacob RodriguezStephen L. BuchwaldBradley L. Pentelute
Engineering Bioactive Dimeric Transcription Factor Analogs via Palladium Rebound Reagents
J. Am. Chem. Soc.,2021,14311788-11798. -
Read more: Extremely Electron-Rich, Boron-Functionalized, Icosahedral Carborane-Based PhosphinoboranesSpokoyny, Alexander M.Lewis, Calvin D.Teverovskiy, GeorgiyBuchwald, Stephen L.
Extremely Electron-Rich, Boron-Functionalized, Icosahedral Carborane-Based Phosphinoboranes
Organometallics,2012,318478-8481. -
Read more: Group 4 metal complexes of benzynes, cycloalkynes, acyclic alkynes, and alkenesBuchwald, Stephen L.Nielsen, Ralph B.
Group 4 metal complexes of benzynes, cycloalkynes, acyclic alkynes, and alkenes
Chemical Reviews,1988,88(7),1047-1058. -
Read more: Improved Process for the Palladium-Catalyzed C–O Cross-Coupling of Secondary AlcoholsHong ZhangPaula Ruiz-CastilloAlexander W. SchuppeStephen L. Buchwald
Improved Process for the Palladium-Catalyzed C–O Cross-Coupling of Secondary Alcohols
Org. Lett.,2020,22(14),5369-5374. -
Read more: Kinetic Modeling Enables Understanding of Off-Cycle Processes in Pd-Catalyzed Amination of Five-Membered Heteroaryl HalidesElaine Reichert RaguramJakob C. DahlKlavs F. JensenStephen L. Buchwald
Kinetic Modeling Enables Understanding of Off-Cycle Processes in Pd-Catalyzed Amination of Five-Membered Heteroaryl Halides
J. Am. Chem. Soc.,2024,146(48),33035-33047. -
Read more: Kinetics and substituent effects in the formation of zirconocene thioaldehyde complexes: .beta.-hydride elimination versus cyclometalationBuchwald, Stephen L.Nielsen, Ralph B.
Kinetics and substituent effects in the formation of zirconocene thioaldehyde complexes: .beta.-hydride elimination versus cyclometalation
J. Am. Chem. Soc.,1988,110(10),3171-3175. -
Read more: Large Increase in External Quantum Efficiency by Dihedral Angle Tuning in a Sky-Blue Thermally Activated Delayed Fluorescence EmitterWenliang HuangMarkus EinzingerAndrea MauranoTianyu ZhuJan TiepeltChao YuHyun Sik ChaeTroy Van VoorhisMarc A. BaldoStephen L. Buchwald
Large Increase in External Quantum Efficiency by Dihedral Angle Tuning in a Sky-Blue Thermally Activated Delayed Fluorescence Emitter
Adv. Optical Mater.,2019,71900476-1900481. -
Read more: Microfluidic electrochemistry for single-electron transfer redox-neutral reactionsYiming MoZhaohong LuGirish RughooburPrashant PatilNeil GershenfeldAkintunde I. AkinwandeStephen L. BuchwaldKlavs F. Jensen
Microfluidic electrochemistry for single-electron transfer redox-neutral reactions
Science,2020,368(6497),1352-1357.