Mn- and Co-Catalyzed Aminocyclizations of Unsaturated Hydrazones Providing a Broad Range of Functionalized Pyrazolines
datasetposted on 11.06.2021, 20:04 by Moritz Balkenhohl, Sebastian Kölbl, Tony Georgiev, Erick M. Carreira
Manganese- and cobalt-catalyzed aminocyclization reactions of unsaturated hydrazones are reported. Whereas manganese catalysis provides access to pyrazoline and tetrahydropyridazine alcohols, cobalt catalysis for the first time paves the way for the selective formation of pyrazoline aldehydes. Furthermore, various functional groups including hydroperoxide, thiol derivatives, iodide, and bicyclopentane may be introduced via manganese-catalyzed ring-forming aminofunctionalization. A progesterone receptor antagonist was prepared using the aminocyclization protocol.
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pyrazoline aldehydeshydrazonebicyclopentaneprogesterone receptor antagonistaminocyclization protocoliodideaccessthiol derivativeshydroperoxideBroad Rangecobalt catalysistetrahydropyridazine alcoholsMnUnsaturated Hydrazonesformationcobalt-catalyzed aminocyclization r...manganese-catalyzed ring-forming am...Functionalized Pyrazolines ManganeseCo-Catalyzed Aminocyclizationsmanganese catalysis