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Open AccessFeature PaperShort Note

9-Aminoquino[2',3':3,4]pyrrolo[2,1-b]quinazolin-11(13H)-one

Department of Pharmaceutical Chemistry, University of Vienna, Althanstraße 14, A-1090 Vienna, Austria
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Molbank 2019, 2019(1), M1050; https://doi.org/10.3390/M1050
Received: 18 February 2019 / Revised: 25 February 2019 / Accepted: 26 February 2019 / Published: 1 March 2019
(This article belongs to the Collection Molecules from Catalytic Processes)
Chemoselective reduction of the corresponding 9-nitro precursor by catalytic transfer hydrogenation afforded the title compound, a new 9-amino derivative of the antitumor alkaloid Luotonin A, in good yield. The structure of the compound was established by means of 1D and 2D 1H-NMR and 13C-NMR spectroscopy as well as by EI-MS and high-resolution ESI-MS. View Full-Text
Keywords: Luotonin A; nitro group reduction; catalytic transfer hydrogenation Luotonin A; nitro group reduction; catalytic transfer hydrogenation
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MDPI and ACS Style

Schneider, E.; Haider, N. 9-Aminoquino[2',3':3,4]pyrrolo[2,1-b]quinazolin-11(13H)-one. Molbank 2019, 2019, M1050.

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