Abstract
A new manganese catalyzed heterocyclization of aminoalcohols has been accomplished. A wide range of heterocycles were synthesized, including 1,2,3,4-tetrahydroquinolines, dihydroquinolinones, and 2,3,4,5-tetrahydro-1H-benzo[b]azepines. The reaction is performed under mild reaction conditions using air and moisture stable manganese catalysts. The desired heterocycles were obtained in good to excellent yields.
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CITATION STYLE
Zubar, V., Brzozowska, A., Sklyaruk, J., & Rueping, M. (2022). Dehydrogenative and Redox-Neutral N-Heterocyclization of Aminoalcohols Catalyzed by Manganese Pincer Complexes. Organometallics, 41(14), 1743–1747. https://doi.org/10.1021/acs.organomet.2c00027
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