Pd/NHC-Catalyzed Enantiospecific and Regioselective Suzuki–Miyaura Arylation of 2-Arylaziridines: Synthesis of Enantioenriched 2-Arylphenethylamine Derivatives | Journal of the American Chemical Society
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Palladium-catalyzed regioselective and stereo-invertive ring-opening borylation of 2-arylaziridines with bis(pinacolato)diboron: experimental and computational studies - Chemical Science (RSC Publishing)
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Catalyst-controlled regiodivergent ring-opening C(sp 3 )–Si bond-forming reactions of 2-arylaziridines with silylborane enabled by synergistic palladi ... - Chemical Science (RSC Publishing) DOI:10.1039/C9SC02507C
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Stereospecific Couplings of Secondary and Tertiary Boronic Esters - Leonori - 2015 - Angewandte Chemie International Edition - Wiley Online Library
J. Am. Chem. Soc. on Twitter: "Stereospecific Acylative Suzuki–Miyaura Cross-Coupling: General Access to Optically Active α-Aryl Carbonyl Compounds @OSUScience @OSU_Chemistry @SNUnow @TotalSyntheses #Stereospecific #Acylative #SuzukiMiyaura ...
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A medial groupoid which does not satisfy left invertive law | Download Scientific Diagram
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Palladium-catalyzed regioselective and stereo-invertive ring-opening borylation of 2- arylaziridines with bis(pinacolato)diboron
Experimental and computational mechanistic investigations a, An... | Download Scientific Diagram
