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• W2285779600 endingPage "2957" @default.
• W2285779600 startingPage "2950" @default.
• W2285779600 abstract "The trisubstituted cyclohexenone 12, generated through a palladium-catalyzed Ullmann cross-coupling reaction between o-iodonitrobenzene and a 4,5-trans-disubstituted 2-iodo-2-cyclohexen-1-one, engaged in a tandem reductive cyclization process upon exposure to hydrogen gas in the presence of Raney cobalt. As a result, the 1,5-methanoazocino[4,3-b]indole 13 was obtained and this could be readily elaborated to the racemic modifications of the alkaloids uleine, dasycarpidone, noruleine, and nordasycarpidone (1-4, respectively)." @default.
• W2285779600 created "2016-06-24" @default.
• W2285779600 creator A5034973943 @default.
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• W2285779600 date "2016-03-17" @default.
• W2285779600 modified "2023-09-24" @default.
• W2285779600 title "Palladium-Catalyzed Ullmann Cross-Coupling/Tandem Reductive Cyclization Route to Key Members of the Uleine Alkaloid Family" @default.
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• W2285779600 doi "https://doi.org/10.1021/acs.joc.6b00240" @default.
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• W2285779600 hasPublicationYear "2016" @default.
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