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- W2777463100 endingPage "1240" @default.
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- W2777463100 abstract "A novel domino reaction of (2-iminoaryl)divinyl ketones with nitromethane was developed for the efficient synthesis of hexahydrophenanthridin-9(5H)-ones. The reaction proceeded smoothly from readily available starting materials under mild reaction conditions to construct three new bonds and two rings with high diastereoselectivities in good to excellent yields in a single step. A mechanism is proposed, involving a stepwise double Michael addition/aza-Henry reaction cascade, and in this transformation, nitromethane acts as a trinucleophile." @default.
- W2777463100 created "2018-01-05" @default.
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- W2777463100 date "2018-01-16" @default.
- W2777463100 modified "2023-10-14" @default.
- W2777463100 title "Triple Nucleophilic Attack of Nitromethane on (2-Iminoaryl)divinyl Ketones: A Domino Synthetic Strategy for Hexahydrophenanthridinones" @default.
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- W2777463100 doi "https://doi.org/10.1021/acs.joc.7b02759" @default.
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