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- W2950794862 abstract "The aldol condensation of an enolisable ketone and a benzaldehyde followed by Michael addition of the enone with a second enolisable ketone under solvent free conditions leads to the quantitative formation of a diketone, which can be readily converted to a pyridine (typically >80% overall yield) via a double condensation in the presence of ammonium acetate in acetic acid, allowing access to a diverse range of oligopyridyls including bipyridyls and terpyridyls." @default.
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- W2950794862 date "2010-05-22" @default.
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- W2950794862 title "ChemInform Abstract: Efficient Synthesis of Pyridines via a Sequential Solventless Aldol Condensation and Michael Addition." @default.
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- W2950794862 doi "https://doi.org/10.1002/chin.200214145" @default.
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