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• W2045431079 endingPage "11873" @default.
• W2045431079 startingPage "11860" @default.
• W2045431079 abstract "A general method is described for the synthesis of 1,3′-bipyrroles. The route involves constructing a pyrrole ring on the nitrogen of a substituted 1H-pyrrole, so as to generate the 1,3′-bipyrrole. In this approach the nitrogen of the starting pyrrole was alkylated with a special Michael acceptor having an allylic leaving group, and the product was then modified in such a way that the second pyrrole ring could be formed by a Paal–Knorr reaction. Two variants of this sequence were examined, one of which led to formation of a 3-hydroxypyridine instead of the second pyrrole ring; the other variant used phenacyl bromide instead of the special Michael acceptor." @default.
• W2045431079 created "2016-06-24" @default.
• W2045431079 creator A5008812976 @default.
• W2045431079 creator A5013699172 @default.
• W2045431079 creator A5090046345 @default.
• W2045431079 date "2013-11-26" @default.
• W2045431079 modified "2023-10-10" @default.
• W2045431079 title "A General Route to 1,3′-Bipyrroles" @default.
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• W2045431079 doi "https://doi.org/10.1021/jo401892t" @default.
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• W2045431079 hasPublicationYear "2013" @default.
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