研究领域
Our research efforts are directed toward developing new classes of ancillary ligands/transition metal complexes that exhibit interesting and unusual reactivity, with the goal of incorporating such reactivity into useful substrate transformations.
近期论文
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Nickel-Catalyzed Monoarylation of Ammonia" A. Borzenko, N. L. Rotta-Loria, P. M. MacQueen, C. M. Lavoie, R. McDonald and Mark Stradiotto* (Angew. Chem. Int. Ed., 2015, 54, 3773-3777).
"Utilizing Mor-DalPhos/Palladium-Catalyzed Monoarylation in the Multicomponent One-Pot Synthesis of Indoles" N. L. Rotta-Loria, A. Borzenko, P. G. Alsabeh, C. B. Lavery and Mark Stradiotto* (Adv. Synth. Catal., 2015, 357, 100-106).
"(N-Phosphinoamidinate)Cobalt-Catalyzed Hydroboration: Alkene Isomerization Affords Terminal Selectivity" A. J. Ruddy, O. L. Sydora,* B. L. Small, Mark Stradiotto* and L. Turculet* (Chem. Eur. J., 2014, 20, 13918-13922).
"Addressing Challenges in Palladium-Catalyzed Cross-Couplings of Aryl Mesylates: Monoarylation of Ketones and Primary Alkyl Amines." P. G. Alsabeh and Mark Stradiotto* (Angew. Chem. Int. Ed., 2013, 52, 7242 –7246).
"Palladium-Catalyzed Cross-Coupling of Aryl Chlorides and Tosylates with Hydrazine." R. J. Lundgren and Mark Stradiotto* (Angew. Chem. Int. Ed., 2010, 49, 8686-8690).
"A P,N-Ligand for Pd-Catalyzed Ammonia Arylation: Coupling of Deactivated Aryl Chlorides, Chemoselective Arylations, and Room Temperature Reactions." R. J. Lundgren, B. D. Peters, P. G. Alsabeh, and Mark Stradiotto* (Angew. Chem. Int. Ed., 2010, 49, 4071-4074).