Stephen L. Buchwald
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Read more: Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditionsTeverovskiy, G.Surry, D. S.Buchwald, S. L.
Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions
Angew. Chem. Int. Ed.,2011,50(32),7312-4. -
Read more: Rapid and Efficient Copper-Catalyzed Finkelstein Reaction of (Hetero)Aromatics under Continuous-Flow ConditionsChen, M.Ichikawa, S.Buchwald, S. L.
Rapid and Efficient Copper-Catalyzed Finkelstein Reaction of (Hetero)Aromatics under Continuous-Flow Conditions
Angew. Chem. Int. Ed.,2014,54263-266. -
Read more: Rational Ligand Design for the Arylation of Hindered Primary Amines Guided by Reaction Progress Kinetic AnalysisRuiz-Castillo, P.Blackmond, D. G.Buchwald, S. L.
Rational Ligand Design for the Arylation of Hindered Primary Amines Guided by Reaction Progress Kinetic Analysis
J. Am. Chem. Soc.,2015,1373085-3092. -
Read more: Reaction of dicyclopentadienylmethylenetitanium with organic halides: Evidence for a radical mechanismBuchwald, Stephen L.Anslyn, Eric V.Grubbs, Robert H.
Reaction of dicyclopentadienylmethylenetitanium with organic halides: Evidence for a radical mechanism
J. Am. Chem. Soc.,1985,107(6),1766-1768. -
Read more: Regio- and Enantioselective Synthesis of 1,2-Diamine Derivatives by Copper-Catalyzed HydroaminationSaki IchikawaXi-Jie DaiStephen L. Buchwald
Regio- and Enantioselective Synthesis of 1,2-Diamine Derivatives by Copper-Catalyzed Hydroamination
Org. Lett.,2019,21(11),4370-4373. -
Read more: Rh-catalyzed asymmetric hydroformylation of functionalized 1,1-disubstituted olefinsWang, X.Buchwald, S. L.
Rh-catalyzed asymmetric hydroformylation of functionalized 1,1-disubstituted olefins
J. Am. Chem. Soc.,2011,133(47),19080-3. -
Read more: Room temperature copper(II)-catalyzed oxidative cyclization of enamides to 2,5-disubstituted oxazoles via vinylic C-H functionalizationCheung, C. W.Buchwald, S. L.
Room temperature copper(II)-catalyzed oxidative cyclization of enamides to 2,5-disubstituted oxazoles via vinylic C-H functionalization
J. Org. Chem.,2012,777526-37. -
Read more: Room-Temperature Copper-Catalyzed Etherification of Aryl BromidesMichael J. StraussMegan E. GreavesSeoung-Tae KimChristiana N. TeijaroMichael A. SchmidtPaul M. ScolaStephen L. Buchwald
Room-Temperature Copper-Catalyzed Etherification of Aryl Bromides
Angewandte Chemie,2024,e202400333. https://doi.org/10.1002/anie.202400333. -
Read more: Room-Temperature Cu-Catalyzed Amination of Aryl Bromides Enabled by DFT-Guided Ligand DesignSeoung-Tae KimMichael J. StraussAlbert CabréStephen L. Buchwald
Room-Temperature Cu-Catalyzed Amination of Aryl Bromides Enabled by DFT-Guided Ligand Design
J. Am. Chem. Soc.,2023,145(12),6966-6975. -
Read more: Schwartz’s ReagentBuchwald, S. L.LaMaire, Susan J.Nielsen, Ralph B.Watson, Brett T.King, Susan M.
Schwartz’s Reagent
Org. Synth.,1993,71(71),77.